3INSERM UMR 1186, Integrative Tumour Immunology and Immunotherapy,
5Department of Biochemistry,
9Thumbay Research Institute of Precision Medicine,
Correspondence Address: Dr. Agnete S. T. Engelsen, Centre for Cancer Biomarkers and Department of Biomedicine, University of Bergen, Jonas Lies vei 91, Bergen 5009, Norway. E-mail: firstname.lastname@example.org
© The Author(s) 2020. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
Epithelial-mesenchymal plasticity (EMP) of cancer cells contributes to cancer cell heterogeneity, and it is well established that EMP is a critical determinant of acquired resistance to cancer treatment modalities including radiation therapy, chemotherapy, and targeted therapies. Here, we aimed to explore how EMP contributes to cancer cell camouflage, allowing an ever-changing population of cancer cells to pass under the radar of our immune system and consequently compromise the effect of immune checkpoint blockade therapies. The ultimate clinical benefit of any combination regimen is evidenced by the sum of the drug-induced alterations observed in the variety of cellular populations composing the tumor immune microenvironment. The finely-tuned molecular crosstalk between cancer and immune cells remains to be fully elucidated, particularly for the spectrum of malignant cells along the epithelial to mesenchymal axis. High-dimensional single cell analyses of specimens collected in ongoing clinical studies is becoming a key contributor to our understanding of these interactions. This review will explore to what extent targeting EMP in combination with immune checkpoint inhibition represents a promising therapeutic avenue within the overarching strategy to reactivate a halting cancer-immunity cycle and establish a robust host immune response against cancer cells. Therapeutic strategies currently in clinical development will be discussed.
Epithelial-to-mesenchymal transition, epithelial-mesenchymal plasticity, immune evasion, tumor immune microenvironment, intrinsic and extrinsic mechanisms of resistance to immune checkpoint blockade, therapeutic opportunity
The history of cancer immunology research dates all the way back to 1863 when Rudolf Virchow observed immune cell infiltration in tumors and hypothesized that sites of chronic inflammation served as a hot bed for cancer development[1,2]. Since then, numerous studies have explored the mechanistic link between chronic inflammation and cancer incidence, and tumor-promoting inflammation has been established as a hallmark of cancer[3-6]. However, in 1909, Paul Ehrlich postulated that the immune system could also have a protective role against tumorigenesis, and this concept was further developed and presented as the “theory of immunosurveillance” by Burnet and Thomas in the 1950’s[8-11]. Despite the fact that these early studies established a link between cancer and the immune system, the importance of the immune system in cancer progression and the therapeutic possibilities for cancer treatment remained largely neglected for nearly half a century. In fact, the theory of immunosurveillance was considered controversial until an important scientific discovery was published in Nature by Shankaran et al. in 2001. The experimental evidence presented in this paper unambiguously showed that the immune system can, and often does, prevent tumors from developing, and that the immune status of mice is a critical determinant of their susceptibility to tumor development induced by chemical carcinogens[12,13].
A malignant cell may reveal its identity and alert the immune system in various ways. During malignant progression, cancer cells accumulate genetic mutations, which in turn may result in the expression of tumor-specific antigens, also known as neo-antigens. In addition, epigenetic alterations may also deregulate the expression of tumor-associated antigens such as cancer embryonic antigens or cancer testis antigens. Both tumor-specific and tumor-associated antigens can be recognized as foreign by the immune system and initiate immune cell-mediated clearing of the malignant cell population[14,15]. However, the strong selection pressure towards cancer cells that continuously expose tumor antigens and markers of cellular distress enforces a continuous interplay between cancer cells and immune cells, referred to as the process of “immunoediting”[9,13]. As a consequence of this constant selection pressure, malignant cells evolve to escape the immune system, and thus the concept of immunoediting could in part explain what was previously considered a controversy: the immune system may contribute to tumor suppression as well as tumor promotion.
Conceptually, the process of immunoediting consists of three sequential phases. In the first phase, the innate and adaptive arms of the immune system work in concert to attack and eliminate the malignant cells (elimination phase). In the second phase, the adaptive arm of the immune system keeps the cancer under control by eliminating some cancer cells while others survive and proliferate, resulting in an equilibrium between dying and proliferating cells in the malignant tissue (equilibrium phase). In this phase, the cells that are still actively dividing will give rise to a population of more or less immunogenic cells, and clonal expansion of less immunogenic cancer cells results in the third phase of the immunoediting process, wherein the tumor escapes from the immune response (escape phase). It is believed that malignancies can remain dormant and asymptomatic in the equilibrium phase of immunoediting for a prolonged period of time, in some cases even an entire lifetime, unless they can eventually “escape” the immune pressure and manifest as symptomatic and clinically detectable cancers. This notion is supported by autopsy studies that have revealed the prevalence of well-differentiated indolent malignancies or “pseudo cancers” of the thyroid, prostate and mammary glands. The onset of the escape phase may be a result of alterations in the cancer cells themselves or through alterations in the tumor immune microenvironment (TIME), leading to an immunosuppressive state[9,13]. As all clinically detectable cancers have successfully escaped the immune response at least to some degree, the process of immunoediting represents a non-linear model where the evolution of the malignant cells and the TIME are mutually dependent on each other. The goal of cancer immunotherapy is to shift the equilibrium of cancer immunoediting from tumor tolerance towards eradication by modulating the crosstalk between malignant cells and the TIME.
William Coley was the first to demonstrate that immune cells can kill cancer cells in patients. Already in 1893, he treated cancer patients with a mixture of bacterial toxins (Coley’s toxins) in a successful attempt to activate the immune system to attack cancers[17,18]. Another approach to boost the immune system to fight cancer has been used for decades in the clinical management of early stage high-risk non-muscle-invasive bladder cancer, where Bacillus Calmette-Guerin, a vaccine originally intended for immunization against M. tuberculosis, is applied as an intravesical immunotherapy to induce a localized immune response[19,20]. However, immunotherapy did not emerge as a revolutionary cancer therapy for multiple cancer types until the recent development of immune checkpoint blockade (ICB) therapy. The concept of ICB is to utilize antibodies to block the receptor-ligand interactions of molecules that serve as negative regulators of the immune system, such as cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and programmed cell death protein 1 (PD-1). Work by Allison and colleagues showed that CTLA-4 functions as an immune checkpoint or “off-switch” by binding CD80/CD86 with greater affinity than the stimulatory “on-switch” CD28, thereby inhibiting activation and proliferation of T cells[21,22]. Ipilimumab (Yervoy®, Bristol-Myers Squibb, New York City, NY, US) is a humanized antibody that blocks CTLA-4, thereby reactivating the immune system. The clinical trials leading to US Food and Drug Administration (FDA) approval of ipilimumab in 2011 received enormous attention, as it was the first cancer treatment ever to demonstrate an increased overall survival in metastatic melanoma patients.
The interaction between the PD-1 receptor and its inhibitory ligand programmed death-ligand 1 (PD-L1) is another example of an inhibitory checkpoint modulating the duration and amplitude of the immune response against cancer cells[24-26]. Interactions between PD-1 and PD-L1 cause inhibition of T cell receptor (TCR)-mediated lymphocyte proliferation and cytokine secretion. In a physiological context, PD-L1 plays an important role in protecting host cells from immune-mediated tissue damage post-infection and preventing autoimmune disorders. PD-L1 is frequently overexpressed by malignant cells, allowing cancers to escape the adaptive immune system. Numerous studies have reported that increased expression of PD-L1 in tumors is associated with poor prognosis[28-31]. Antibodies blocking the PD-1/PD-L1 axis have been shown to induce durable clinical responses in numerous cancer types including malignant melanoma[22,23,32], non-small cell lung cancer (NSCLC)[33,34], urothelial carcinoma[35,36], head and neck squamous cell carcinoma, Hodgkin’s lymphoma and renal cell carcinoma (RCC)[32-34,37-39]. This has led to FDA approval of several immune checkpoint inhibitors including the fully humanized monoclonal PD-L1-targeting antibodies atezolizumab (Tecentriq®, Genentech/Roche, South San Francisco, CA, US) and durvalumab (Imfinzi®, AstraZeneca, Cambridge, UK), as well as monoclonal antibodies targeting PD-1; namely pembrolizumab (Keytruda®, Merck Sharp & Dohme, Kenilworth, New Jersey, US) and nivolumab (Opdivo®, Bristol-Myers Squibb, New York City, NY, US)[35,36,40,41].
ICB truly represents a paradigm shift in cancer treatment; not only do some patients experience profound clinical benefit from the treatment, but also it has been shown to induce durable responses for a subset of patients with aggressive malignancies[42,43]. Unfortunately, some of the most common cancers such as breast, prostate and colon cancer have shown poor responses to ICB[37,44]. Furthermore, even within the subtypes of cancers for which ICB therapy is indicated, heterogeneous responses have been shown, and a majority of the patients do not benefit from ICB therapy. Furthermore, heterogeneous responses have been observed between multiple cancer lesions within the same patient. The European Organisation for Research and Treatment of Cancer 18071 trial reported that more than half of high-risk patients with stage III melanoma who received adjuvant ipilimumab relapsed with a median recurrence-free survival of 26.1 months. The KEYNOTE-001 trial reported that one in four patients with metastatic melanoma who achieved an initial objective response to pembrolizumab subsequently experienced disease progression. However, the reported outcomes of the efficacy of pembrolizumab treatment either alone or in combination with other treatments for advanced/metastatic melanoma varies considerably in the multiple studies performed, and a recent meta-analysis including 25 research articles with a total of 2,909 patients reported an overall response rate of only 34% (progression-free survival: 5.7 months, overall survival 20.3 months).
Multiple mechanisms have been proposed to explain why only a subset of tumors respond to ICB, yet an urgent lack of reliable predictive biomarkers remains[37,42,47]. High cancer cell expression of immune checkpoint ligands, high tumor mutational burden (TMB) and a favorable immune cell infiltration in the TIME, i.e., immune cell inflamed “hot” as opposed to immune cell excluded “cold” tumors, have all been associated with a more favorable response to ICB[37,48,49]. The best predictive biomarkers identified so far include the TMB and neoantigen landscape of the tumor; however the adoption and harmonization of these methods in the clinic remain in their infancy[15,50,51]. For lack of better alternatives, PD-L1 expression is currently being used as a predictive biomarker for immune checkpoint inhibitors targeting the PD-1/PD-L1 axis in malignant melanoma, NSCLC and RCC, but the usefulness of PD-L1 expression as a predictor of response to ICB remains a continuous matter of debate[42,52]. Thus, extensive efforts are currently being made to identify better predictive biomarkers and explore rational combinational therapies, with the ultimate aim to increase initial ICB response rates while also preventing or reversing the emergence of resistance[49,53].
In this review, we aim to explore how epithelial-mesenchymal plasticity (EMP), i.e., the acquired ability of epithelial cells to transition between epithelial and mesenchymal phenotypes, might contribute to cancer cell camouflage, enabling an ever-changing population of cancer cells to escape the immune system. Targeting EMP represents a promising therapeutic opportunity in combination with immune checkpoint inhibitors. Here, we aim to elucidate how EMP affects the various steps of the cancer-immunity cycle and to highlight some of the clinical evidence and molecular mechanisms supporting the hypothesis that targeting EMP represents a promising therapeutic avenue within the overarching strategy to reactivate a halting cancer-immunity cycle and establish a robust host immune response against cancer cells.
The majority of human cancers are of epithelial origin. As opposed to mesenchymal cells, which are characterized by their spindle-shaped fibroblast-like morphology and loose connection to surrounding cells, epithelial cells exhibit highly organized apicobasal polarity and junctional complexes ensuring stable intercellular adhesion and controlling transepithelial permeability. The process of epithelial-to-mesenchymal transition (EMT) was first described in embryonic development[55-57], but was later associated with physiological and pathological processes occurring in adults such as wound healing, in the progression of carcinoma and indirectly in tissue fibrosis[58-63]. EMT is a cellular process where epithelial cells lose their cell polarity and tight cell-cell adhesions, acquiring a fibroblast-like morphology and cytoarchitecture as well as the ability to remodel the extracellular matrix (ECM) and alter their cellular behavior to gain more migratory and invasive properties[55,62,64]. Considerable remodeling of the cytoskeleton accompanies the loss of epithelial cell polarity and confers new mechanobiological properties favoring migration and tissue invasion[62,63]. At the molecular level, EMT is characterized by downregulation of epithelial markers (e.g., E-cadherin and EpCAM), and upregulation of mesenchymal markers (e.g., N-cadherin and vimentin). Mesenchymal cells also exhibit increased expression of matrix metalloproteinases which are required for their invasive properties[65,66]. The most commonly recognized EMT transcription factors (TFs) include Snail (SNAI1), Slug (SNAI2), zinc finger E-box binding homeobox 1 and 2 (ZEB1 and ZEB2), and Twist family BHLH transcription factor 1[62,67]. Since multiple TFs may activate EMT, different combinations of TFs may be responsible, at least in part, for the heterogeneity that stems from different versions of the EMT program. Of note, the EMT International Association suggests that EMT should not be assessed solely on the basis of EMT-TF expression or that of a small number of molecular markers, but rather the primary criteria for defining EMT should consist of measurable alterations in cellular characteristics together with a set of molecular markers.
Importantly, EMT is not an irreversible linear process, and the reverse process, mesenchymal-to-epithelial transition (MET), describes the transition from the mesenchymal (M) to the epithelial (E) state. Although EMT was initially believed to be a binary process, it is now well documented that this is indeed a dynamic process and intermediate-state cells also exist[61,69]. Cells can thus undergo partial EMT or partial MET to obtain intermediate E/M states with a cellular phenotype that is neither completely epithelial nor completely mesenchymal and harbors attributes characteristic of both states[62,69]. Rather than acting as an “on/off” switch between the E and M states, the process of EMT is therefore considered to generate a continuum of cell states along an “epithelial-mesenchymal axis”, also frequently referred to as an “EMT scale” or “EMT spectrum”[60,70]. Tan and colleagues have developed a universal and quantitative gene expression-based EMT scoring system used to establish and evaluate an EMT spectrum across different cancer types. Recently, the term “epithelial-mesenchymal plasticity” (EMP) has been increasingly recognized, referring to the ability of cells to adopt mixed E/M features and to switch between various states along the epithelial-mesenchymal spectrum. Although carcinoma cells may hijack this conserved developmental program, its physiological role in maintaining homeostasis is highly regulated both spatially and temporally, while the pathological EMT program detected in cancers, on the other hand, appears to be a mainly stochastic and time-independent process[65,66,71]. Of note, non-epithelial cancers such as melanoma have also been shown to undergo EMT-like programs leading to similar phenotypic changes induced by EMT-related genes, and serve as a model system for studying metastasis and therapy resistance[72-74]. Phenotypic switching in melanoma involves re-organization of the cytoskeleton, cell membrane and cellular adhesions, as well as alterations in common EMP-related phenotypic markers including gain of E-cadherin and loss of N-cadherin expression.
Under pathological conditions, epithelial cells are believed to undergo EMT, but they rarely or perhaps never undergo the full EMT transition to obtain a completely mesenchymal phenotype, suggesting that partial EMT represents the norm rather than the exception[60,62]. Evidence also indicates that these intermediate E/M phenotypes have the greatest malignant and metastatic potential[75-77]. Carcinoma cells can also temporarily transition to a more plastic state to metastasize or overcome selection pressures from therapy and subsequently revert to an epithelial-like state. Expression of EMT-TFs is also frequently accompanied by features of stemness. Retention of stemness has been linked to EMT and in particular to a stemness window around intermediate E/M states. Like EMP, the acquisition of stem cell traits in cancer cells is not considered a fixed trait; rather it represents a hallmark of cancer within a spatial and temporal window in cancer progression. Accumulating evidence suggests that morphological phenotype and stemness can be regulated independently in malignant cells, but that a stemness window along the EMT axis may predispose malignant cells for acquisition of stem cell traits.
Even for the most effective cancer therapies, be it chemotherapy, targeted therapies, radiotherapy or immunotherapy, persisting cancer cells that survive treatment are believed to constitute a reservoir of slow-cycling cells that eventually may acquire irreversible genetic mutations or epigenetic alterations causing therapy resistance and relapse[78-80]. Acquired therapy resistance is one of the major obstacles to achieving durable remission, and thus major efforts have been made to understand the mechanisms of drug resistance against targeted therapies as well as more conventional cancer treatment regimens. Historically, the focus of this research has been to uncover genetic mutations responsible for acquired drug resistance, such as secondary mutations in the target gene, causing impaired drug binding, or mutations causing activation of downstream signaling or alternative survival pathways[78,81]. However, recent attempts to characterize resistance mechanisms to targeted therapies, such as that of third-generation anaplastic lymphoma kinase (ALK) inhibitor loratinib resistance by next-generation sequencing and phenotypic analysis of longitudinal tumor samples, have highlighted EMT as a mediator of resistance in cases where a specific mutation affecting drug binding could not be detected. Furthermore, the EMT-mediated loratinib resistance found in these patient-derived cell lines could be overcome by combined SRC and ALK inhibition. EMP has been shown to be widely associated with therapy resistance against both cytotoxic and targeted therapy in multiple cancer types, and increasing evidence also shows that EMP contributes to a multidrug resistance phenotype[58,60,71,83]. However, the exact mechanism by which EMP contributes to drug resistance in these various contexts remains to be fully elucidated. Proposed mechanisms include reduced levels of pro-apoptotic proteins or increased drug efflux, which may be part of a broader association between EMT-mediated cancer cell dedifferentiation, acquisition of stem cell traits, and drug resistance[78,83-87]. Although it has been acknowledged for quite some time that dynamic chromatin modifications may be an independent route to drug resistance in cancer cells and thus embodies a promising drug target in combination with various drugs including ICB, it was not until the recent FDA approval of tazemetostat (Trade name: Tazverik, developer: Epizyme), a first-in-class small molecule inhibitor of enhancer of zeste homolog 2 (EZH2), that this hypothesis has been feasible for clinical testing. Tazemetostat was FDA approved as a monotherapy in January 2020 for patients with histologically confirmed, metastatic or locally advanced epithelioid sarcoma with INI1 loss, and was thus the first “epigenetic” drug approved for solid cancers. EZH2 is considered a master regulator of EMT through orchestrating the regulation of the H3K27me3 epigenetic mark, and in pancreatic cancer it has been shown to regulate EMT through miRNA 139-5p. Tazemetostat is currently in phase 2 clinical trials in combination with the PD-1 inhibitor TecentriqTM (atezolizumab) in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), and thus future combination studies will need to address whether EZH2 inhibitors or other epigenetic drugs can reduce EMT and increase response to ICB in pancreatic cancer or other solid cancers.
Novel technologies leveraging single cell analysis have only just begun to provide a better mechanistic understanding of the processes at play. In several recent studies in vitro, drug-tolerant persister cells, sometimes referred to as “jackpot” cells, have been observed in cancer cell cultures from a variety of tumor types upon treatment[78,80,88-91]. From single-cell sequencing endeavors, these studies have shown that many cancers, including melanoma, display a profound transcriptional variety at the single cell level. Through single-cell gene expression analyses of melanoma cultures, Shaffer and colleagues were able to demonstrate that non-heritable resistance to the V600E mutated BRAF inhibitor vemurafenib (Zelboraf, Plexxikon and Genentech) was established from a very rare (1 per 50-500 cells) subpopulation of pre-existing pre-resistant cells. These cells transiently express a semi-coordinated set of well-known plasticity and resistance markers, including epidermal growth factor receptor (EGFR), platelet derived growth factor receptor beta, nerve growth factor receptor, fibroblast growth factor receptor 1, Wnt family member 5A (WNT5A), JUN and the receptor tyrosine kinase AXL. Treatment with vemurafenib induced a stepwise reprogramming of the pre-resistant cells into a stable resistant phenotype, which was not affected by drug holidays.
AXL expression in melanoma has been associated with resistance mechanisms mediated by mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) signaling[92-94]. Tirosh and colleagues provided strong evidence for the involvement of AXL as well as AXL-related genes (AXL signature) in acquired melanoma resistance to both vemurafenib and the MEK inhibitor trametinib (Mekinist, Novartis, Basel, Switzerland), and also found that the proportion of a similar population of “jackpot” cells as well as the abundance of plasticity gene transcripts significantly increased after resistance was acquired in vitro, while being selected against more differentiated populations expressing melanocyte-inducing transcription factor (MITF) and SRY-box transcription factor 10. Taken together, the accumulating evidence for the role of rare “jackpot” cells in acquired therapy resistance supports the hypothesis that intervention with cytotoxic or targeted therapies and immunotherapies displaying initial efficacy in tumor eradication may also act as selection pressures, predisposing tumors to immune evasion through the acquisition of plasticity phenotypes and priming cells for immune resistance. The adoption of distinct phenotypes through the process of EMT may provide cells with properties adaptive to changes in the TIME, and thus act as drivers towards a phenotypic state independent of the drug-targeted pathways.
The tumor microenvironment is a key regulator of EMP, which may be induced by combinations of multiple microenvironmental factors including hypoxia, pH, ECM composition, tensile forces and the presence of soluble factors such as interferons, inflammatory cytokines and growth factors[61,65,66,86,96-98]. Hypoxia occurs in most actively growing solid tumors and is an important EMT inducer. Accumulating evidence also suggests that hypoxic stress is linked to therapy resistance as well as regulation of tumor immunogenicity and both tumor and immune plasticity[99,100]. Hypoxic areas of growing tumors have been shown to attract immunosuppressive cells such as myeloid-derived suppressor cells (MDSCs), tumor-associated macrophages (TAMs) and regulatory T cells (Tregs), and hypoxia has also been shown to upregulate PD-L1 on MDSCs[102,103]. Targeting hypoxia has thus been suggested to improve the efficacy of cancer immunotherapy[102,104,105]. Remodeling of ECM through secretion of specific matrix MMPs and new ECM components, namely collagen type 1, has been shown to induce EMT through both mechanotransduction and direct membrane receptor signaling through integrins and DDR1/2[106-108]. Cancer-associated fibroblasts (CAFs), in addition to their role in ECM remodeling, serve as one of the primary sources of key EMT-inducing growth factors including hepatocyte growth factor (HGF), fibroblast growth factor, interleukin (IL)-6 and transforming growth factor-beta (TGF-β); however, molecular profiling and ablation of heterogeneous CAF subsets in various tumor models have shown conflicting and context-dependent effects on the efficacy of different therapies. Thus, for CAFs and other cellular components of the TIME, the continuum of cells along the differentiation/polarization axis is far more complex than previously anticipated and remains to be explored further by high-dimensional analyses.
Multiple studies have demonstrated that the TIME strongly contributes to the induction of the EMT program and subsequent tumor progression. Cells of the TIME that are involved in regulating EMP include TAMs, MDSCs, neutrophils and natural killer (NK) cells[110,111]. TAMs have a major role in orchestrating cancer-related inflammation, and pro-inflammatory macrophages have been shown to induce EMT at the invasive margin of the tumor through inflammatory cytokine tumor necrosis factor-α (TNF-α)-mediated stabilization of the transcription factor SNAI1 via nuclear factor-κB (NF-κB) pathway activation, while knockdown of SNAI1 suppressed inflammation-mediated breast cancer metastasis, suggesting a mechanism for EMT as a regulator of inflammation-induced metastasis. Macrophages have also been shown to induce EMT in intratumoral cancer cells via TGF-β secretion and activation of the β-catenin pathway. In a murine melanoma model, MDSCs were shown to infiltrate the tumor and induce EMT in vivo. Functional in vitro assays with purified MDSCs revealed that the TGF-β, epidermal growth factor (EGF) and HGF signaling pathways were all involved in MDSC-induced EMT activation of cancer cells. In a similar model, HGF secretion by T cell-inflamed TIMEs was shown to mobilize and recruit neutrophils through binding and activation of c-MET, wherein they gained immunosuppressive properties. Neutrophils are also frequently enriched at the invasive margin of gastric cancers, and in a recent study, tumor-associated neutrophils were shown by in vitro co-culture experiments to promote EMT in gastric cancer cells via IL-17α signaling. Although the mechanisms are still unclear, NK cells may increase the malignancy of melanoma cells by inducing an EMT-like switch.
The finely tuned, step-wise process by which the immune system can efficiently recognize and eradicate cancer cells was first conceptualized by Chen and Mellman and is now widely known as “the cancer-immunity cycle”. In the first step of the cancer-immunity cycle, cancer antigens are recognized and captured by professional antigen-presenting cells (APCs), such as dendritic cells (DCs). Alarmins or damage-associated molecular patterns (DAMPs) released by dying tumor cells may aid in the attraction of APCs to the tumor bed[118,119]. This initiation of the cancer-immunity cycle is dependent on the APCs capturing both cancer specific antigens expressed by the cancer cells (immunogenicity) as well as signals that specifically evoke an immune response (adjuvanticity)[117,120]. Toll-like receptors (TLRs) are expressed on DCs and are key mediators bridging innate and adaptive immunity once stimulated by foreign pathogen associated molecular patterns (PAMPs) or DAMPs. TLR activation results in the secretion of pro-inflammatory cytokines including IL-6, IL-12, TNF-α, and type I interferons, which in turn serve to recruit immune effector cells. The APCs from step one of the cancer-immunity cycle travel from the tumor microenvironment to the lymph node where they present captured cancer related antigens to T cells (step 2). T cells can then be activated and programmed to specifically react to these antigens (step 3). Activated cytotoxic T lymphocytes (CTLs) then travel back to the tumor site (step 4) where they are then able to infiltrate the tumor (step 5), recognize (step 6) and kill (step 7) the antigen-presenting cancer cells. All these steps need to be intact for the cancer-immunity cycle to be successfully completed.
As discussed below, EMT may affect several steps of the cancer-immunity cycle and thus hinder progression in this finely-tuned cycle in multiple ways [Figure 1]. One of the remaining challenges will be to identify the “Achilles heel” of individual cancer cases and tailor the treatment to initiate a robust cancer-immunity cycle. We suggest that targeting cancer EMP may represent a unique opportunity to bolster several steps of the cancer-immunity cycle. Although the molecular mechanisms of EMP affecting the various steps of the cancer-immunity cycle are still largely obscure, targeting EMP represents a promising therapeutic addition within the overarching strategy of personalized cancer immunotherapy to re-activate a halting cancer-immunity cycle and re-establish a robust host immune response against the cancer cells[53,121].
Figure 1. EMP affects various steps of the cancer-immunity cycle. The therapeutic rationale for targeting EMP in combination with ICB is based on the fact that EMP affects multiple steps of the cancer-immunity cycle described by Chen and Mellman. Briefly, targeting EMP can induce an increased release of DAMPs serving as an adjuvant during the release of cancer cell antigens (STEP 1). DAMPs are further recognized by pattern recognition receptors (PRRs) including TLRs. EMP targeting can induce an M1 to M2 polarization of macrophages and an activation of APCs, and thus aid in cancer antigen presentation (STEP 2). Targeting EMP and the EMP-associated immunosuppressive tumor immune microenvironment (TIME) can enable the infiltration of educated T cells into the cancer (STEP 5). EMP is associated with reduced recognition (STEP 6) and immune effector cell-mediated killing (STEP 7) of cancer cells, and targeting EMP can therefore induce increased effector cell-mediated lysis of cancer cells and propagation of the cycle. Adapted courtesy of Chen and Mellman. EMP: epithelial-mesenchymal plasticity; ICB: immune checkpoint blockade; DAMPs: damage-associated molecular patterns; APCs: antigen-presenting cells
Using hypoxia-inducible factor 1-alpha (HIF1 alpha) and AXL inhibitors as examples, the rationale behind clinical trials combining ICB and mediators of epithelial phenotypic plasticity are based on the effects of these drugs on multiple steps of the cycle. First, cancer treatments that induce immunogenic cell death (ICD) have been shown to contribute to anticancer immune attack, mediated by the exposure of DAMPs. Hypoxia is a strong microenvironmental factor that supports coordinated induction of EMT and also AXL expression and autophagy. The HIF1 alpha inhibitor PX-478 was also recently shown to enhance gemcitabine-induced immune responses and eliminate pancreatic ductal adenocarcinoma (PDAC) cells through induction of ICD. EMT correlates with autophagy induction, and pre-mortem stress-related autophagy is also linked to the release of DAMPs and induction of ICD[53,123]. Thus, the impact of targeting autophagy to increase the efficacy of immune checkpoint inhibition is expected to be seen particularly in cancers of an immune cold or immune-excluded immunophenotype. We have recently shown that the small molecule AXL inhibitor bemcentinib abrogates the autophagic flux and is a potent inducer of ICD; this is of particular interest as it implicates a favorable adjuvant effect and alteration of the TIME upon AXL inhibition in immunogenic but immunosuppressed tumors[53,124]. In this context, it is important to note that the increased danger signaling per se is not sufficient to compensate for the intrinsically low immunogenicity of some tumors, and that the effect of autophagy-dependent danger signaling is solely expected to warm up immune cold tumors and elicit a strong immune response in immunogenic tumors. Increased immunoadjuvanticity, that is, the recruitment of professional APCs to educate the naïve T lymphocyte population, is critical to maximize the potential therapeutic benefit of ICB. Furthermore, AXL has been shown to suppress antigen presentation by downregulating major histocompatibility complex I (MHC-I), and genetic ablation of AXL in the experimental PyMT-induced tumor model was shown to induce MHC-I expression to even higher levels compared to IFN-γ-induced parental cells. AXL inhibition enhances cytokine release and increases CD8+ T cell response in syngeneic models, resulting in an elevated cytotoxic T cell-dependent antitumor immune response after radiation, which could be further enhanced by ICB.
Carcinoma subclones with pronounced mesenchymal phenotypes emerging from sustained hypoxic stress of primary NSCLC cells in culture were shown to be less susceptible to NK and CTL cell-mediated lysis compared to subclones with a more epithelial phenotype. This difference was associated with reduced expression of intercellular adhesion molecule 1 (ICAM1), UL16 binding protein 1 (ULBP1), and MHC-I as well as increased TGF-β expression in mesenchymal subclones. It was shown that expression of AXL in the mesenchymal NSCLC clones was correlated with an increased cancer cell intrinsic resistance to immune cell-mediated killing by NK cells as well as autologous CTLs while AXL targeting via small molecule inhibition potently sensitized mesenchymal lung cancer cells to cytotoxic lymphocyte-mediated killing. These findings raise the intriguing possibility that phenotypic plasticity may enable tumor cells to circumvent NK- and CTL-mediated cell killing. This has also been attributed to the associated cytoskeletal remodeling in tumor cells, interfering with immune synapse formation[96,128,129]. This process may provide a rationale to test EMP-targeting approaches to enhance antitumor immunotherapy[95,130,131].
The EMT-TF SNAI1 has been shown to have a strong impact on the cancer-immunity cycle. In human mammary carcinoma MCF7 cells, Akalay et al. observed that overexpression of exogenous SNAI1 correlated with increased mesenchymal and stemness traits in these cells while reducing their susceptibility to CTL-mediated lysis. This was in part explained by reduced MHC expression in the SNAI1-transfected MCF7 derivatives and concomitant reduced activity of TCR signaling at the site of cell-cell contact (immunological synapse). Similar observations were reported using another MCF-7 derivative displaying hyperactive TGF-β signaling. Likewise, SNAI1 overexpression in murine B16 melanoma cells resulted in inhibition of CTL lysis activity, inhibition of DC maturation and expansion of suppressive Treg-like CD4+ Foxp3+ cells in a mechanism involving thrombospondin (TSP1) and TGF-β secretion. Using PyMT cells, a murine transplantable model of breast cancer carcinoma, Dongre and colleagues showed that tumors arising with a more mesenchymal phenotype and high expression of SNAI1 expressed more PD-L1 and less MHC-I and had less cytotoxic T cells, but were enriched for immunosuppressive components including M2 macrophages and Tregs. The link between EMP and the presence of immunosuppressive macrophages seems to be critical. Although the mechanisms are still unclear, it is tempting to speculate the involvement of immunosuppressive chemoattractants (e.g., TGF-β) in the recruitment of macrophages to the TIME. Another interesting observation made by Dongre and colleagues was that NK cells infiltrate mesenchymal tumors more effectively compared to the epithelial tumors, which can be explained by downregulation of MHC-I in the more mesenchymal tumors. However, despite this NK enrichment, the mesenchymal tumors rapidly grow in this model suggesting intrinsic or extrinsic resistance as well as possible cooperative effects.
Converging preclinical evidence also suggests that tumors with a more EMP/mesenchymal phenotype are less responsive to ICB. SNAI1+ melanoma tumors were unresponsive to immunotherapy, but targeting SNAI1 with siRNA or anti-TSP1 monoclonal antibody could inhibit tumor progression and induce systemic immune responses. In ZEB1/miR-200-driven NSCLC models as well as in SNAI1-driven breast cancer models, EMP was associated with PD-L1 expression. Targeting PD-L1 in NSCLC efficiently prevented tumor growth and metastasis. In PyMT breast cancer models, epithelial tumors were susceptible to elimination by anti-CTLA-4 immunotherapy, whereas corresponding mesenchymal tumors were refractory to such treatment. By injecting E/M cells at various ratios, these investigators also elegantly demonstrated that in the case of mixed epithelial-mesenchymal tumors, even the presence of rare mesenchymal carcinoma cells could protect the epithelial counterpart from anti-CTLA-4 treatment by promoting the recruitment of immunosuppressive cells including M2 macrophages and Tregs.
Sharma and colleagues have described three different categories of resistance against immunotherapy: primary, adaptive and acquired resistance. Primary, or innate, resistance to immunotherapy occurs when the cancer does not have an initial response (i.e., it is refractory) to the therapy. Adaptive resistance occurs when the tumor is initially recognized by the immune system, but the tumor adapts to escape immune attack. Given the evolving nature of the interaction between immune cells and cancer cells in this process, adaptive resistance can manifest clinically as either primary resistance, mixed responses or acquired resistance. Thus, only clinical data describing the role of EMP in primary and acquired resistance will be discussed here. Acquired resistance describes the clinical scenario in which the cancer initially responded to immunotherapy but recurs and progresses after a period of time. However, as Sharma and colleagues emphasize in their review, the immune response is dynamic and can evolve for each patient and tumor, and could also be affected by environmental and genetic factors as well as by the cancer treatment. Accordingly, it is important to note that the process of immunoediting mentioned above is anything but a static process, as novel rounds of therapy and subsequent immunoediting affect the composition of the TIME through clonal selection acting on pre-existing cancer cell populations or de novo acquisition of resistant traits.
The hypothesis that epithelial phenotypic plasticity could be a key determinant of the outcome of immune checkpoint inhibition in cancer is fueled by pioneer transcriptional data. Hugo and colleagues performed exome and transcriptomic sequencing of melanoma pre-treatment samples, and a common gene signature was shown to characterize tumors that were non-responsive to anti-PD-1 therapy. This innate PD-1 resistance (IPRES) gene signature encapsulates the upregulation of EMT transcription factors, immunosuppressive cytokines, and pro-angiogenic factors. The IPRES signature, enriched in non-responding patients, overlaps with signatures for wound-healing, angiogenesis, ECM remodeling, cell adhesion, monocyte/macrophage chemotaxis and resistance to MAPK pathway inhibition. Data from The Cancer Genome Atlas (TCGA), PROSPECT, and BATTLE-1 showed that inflammatory changes in the tumor microenvironment were strongly associated with induction of EMT signatures in lung adenocarcinoma, which in turn correlated with upregulation of multiple suppressive immune checkpoint receptors or their ligands, including B7-H3, CTLA-4, PD-1, PD-L1, PD-L2, B and T lymphocyte attenuator, and T cell immunoglobulin and mucin-domain containing-3 (TIM-3). Taken together, these data suggest that attenuating the mechanics underlying the IPRES signature may have the potential to enhance anti-PD-1 responses in melanoma and other cancers. Intriguingly, the receptor tyrosine kinase AXL, whose upregulation is associated with a reversible plasticity cell state and is part of the “jackpot” signature of pre-existing pre-resistant cells, was found to be a component of the IPRES signature among 532 upregulated genes including several EMT and EMP mediators such as EGFR, NGF, CDH11, EPHA3, HEY1, HEY (NOTCH effectors), TWIST2, ID3, ID1, many interleukins including immunosuppressive IL10, ITGA5/8; LOX, LOXL2, MMP1, MMP2, MMP3, MMP9, NRP1, THBS1 and THBS2, NUMBL (plasticity factor), ROR2, RORB, RUNX2, SEMA3A SERPINE1 VEGFA, VEGFC and Wnt genes WNT11 WNT2 WNT5A WNT7B and DKK3. Among the 161 genes downregulated in the IPRES signature are HLA-A and E-cadherin (CDH1).
In line with these findings from melanoma, Thompson and colleagues recently observed that NSCLC tumors displaying a more mesenchymal phenotype showed reduced clinical responses to ICB. In this study, an EMT/inflammation-based signature had clinical utility in predicting clinical response, supporting the view that the EMP signature is an adverse predictor of ICB response across tumor types.
Furthermore, in urothelial cancer patients with T cell-infiltrated tumors, a higher EMT/stroma-related gene expression signature was associated with poor response and disease progression under anti-PD-1 therapy. This study suggested that stromal elements are the major source of immune resistance in this setting, thus providing a rationale for co-targeting PD-1 and the stromal elements mediating resistance.
Potential mechanisms of acquired resistance to immunotherapy include loss of T-cell function, downregulation of tumor-associated antigen presentation, and acquisition of mutations that enable immune escape. The IFN-γ pathway plays an important regulatory role at the center stage of primary, adaptive and acquired resistance to ICB. IFN-γ, which is secreted primarily by T cells and NK cells, is crucial to initiate an effective antitumor immune response as it mediates increased MHC-I expression, recruitment of immune cells and direct antiproliferative and pro-apoptotic effects in cancer cells. However, constitutive IFN-γ exposure might initiate immunoediting and subsequent immune escape by promoting alteration of the molecules involved in IFN signaling pathways such as Janus kinase/signal transducers and activators of transcription (JAK/STAT) and induction of EMT. For example, an increased frequency of IFN-γ pathway gene mutations in tumors of melanoma patients that did not respond to the anti-CTLA-4 antibody ipilimumab has been shown[37,138]. Mutations in the IFN-γ pathway could also result in lack of IFN-γ-induced PD-L1 expression causing primary resistance to PD-1 blockade[37,139].
Cancer cell activation of the Wnt/β-catenin pathway or activation of the phosphoinositide 3-kinase (PI3K)/AKT signaling pathway, through, e.g., acquired loss of the tumor suppressor protein phosphatase PTEN, have both been shown to regulate EMT, and both signaling pathways have been mechanistically linked to immune resistance in preclinical studies[140-144]. Trujillo and colleagues performed a molecular analysis of baseline and treatment-resistant tumor samples from two malignant melanoma patients who initially showed a durable partial response to either a melanoma-peptide/interleukin-12 vaccine or combined anti-CTLA-4 + anti-PD-1 therapy and subsequently developed new treatment-resistant metastases. Transcriptional profiling and genomic sequencing for oncogenic alterations as well as histologic analysis for T cell infiltration were performed to investigate mechanisms of acquired resistance to immunotherapy. In the first case, the authors found increased tumor cell intrinsic activation of β-catenin in the patient’s treatment-resistant metastasis, whereas in the second case genomic sequencing revealed acquired biallelic PTEN loss, while both cases were associated with loss of T cell infiltration. This study highlights that continued analysis of acquired resistance samples is crucial to identify potentially targetable resistance pathways amenable to therapeutic intervention.
Expression of IL8 by tumor cells has been shown to promote their EMP. Thus, IL8 and its receptor CXCR1/2 axis have been established as potential EMP regulating factors and subsequent targeting of the IL8/CXCR1/2 axis has been explored as a promising EMP target. Preclinical studies have also been performed combining CXCR1/2 blockade with bifunctional anti-TGF-β RII/PD-L1. In this study, Horn and colleagues were able to show that simultaneous inhibition of TGF-β, PD-L1 and CXCR1/2 in murine breast and lung cancers synergized to reverse EMP and associated mesenchymal features, reduce infiltration by immunosuppressive MDSCs, and enhance T cell infiltration and overall antitumor immune response.
Combination therapies being tested that seek to enhance the immune response have been extensively reviewed elsewhere[49,146]. From the discussion above, it is evident that it is not clear which combination of the multifaceted characteristics of EMP drives the prominent resistance to ICB, and thus it is also not clear how EMP may be targeted most effectively in various cancer contexts. The multiple pathways involved in the initiation and maintenance of epithelial plasticity and the redundancy between these overlapping pathways makes EMP a challenging target. Attempts are being made to target EMP through the multitude of soluble factors, receptors, and transcription factors involved. Several combinations with ICB have been explored in preclinical models, and a few trials have been initiated based on the hypothesis that EMP is one of the main mediators compromising the efficacy of ICB therapies and that targeting EMP could lead to stronger and more durable ICB responses [Table 1]. Here, we will specifically highlight promising therapeutic agents targeting EMP-mediated mechanisms of ICB resistance and discuss them in light of the available mechanistic data to support their multifaceted mechanism of action within the TIME.
Clinical trials where EMP targets are being evaluated in combination with ICB targeting the PD-1/PD-L1 axis
|Target||Drug name||Type||Cancer type||Latest phase*||Clinical trial number**|
|TGF-βRI||Vactosertib + durvalumab||Selective TKI||Urothelial||II||NCT04064190|
|TGF-βRI||LY3200882||Selective TKI||Advanced cancer||II||NCT04158700|
|PD-L1/TGF-βRII||Bintrafusp-alfa||AntiPD-L1/TGFbetaRII fusion protein||NSCLC||III||NCT03631706|
|(TYRO3, AXL, MER)/KIT/VEGFR2||Sitravatinib||Pan-TKI||NSCLC||III||NCT03906071|
TGF-β is a major regulator of the tumor microenvironment, and also a potent inducer of cancer cell EMT and immune suppression[61,86,97,98]. TGF-β is being explored as a target for combination with ICB. Recent retrospective and preclinical reports highlight its role in ICB resistance, while mechanistic and clinical studies continue to refine targeting strategies and synergy with checkpoint blockade. TGF-β is expressed in cancer, stromal and immune cells in three isoforms, TGF-β1, β2, and β3. Several pan-cancer gene expression analyses have shown that TGF-β1 is the primary isoform expressed in tumors, while TGF-β3 is less frequently observed and TGF-β2 is rarely detected and mainly serves to regulate normal cardiac function and hematopoiesis, which helps explain the failure of earlier pan-TGF-β targeting therapies due to toxicity-related adverse events[108,147,148]. The most common proposed mechanisms of TGF-β-driven ICB resistance are CD8+ T cell exclusion via fibroblast differentiation and subsequent stromal remodeling and inhibition of CD4+ T helper cell differentiation to the immune-activating T-helper (Th)1 effector cell phenotype, as these conditions have been reproduced in various mouse tumor models and effectively treated by combined targeting of TGF-β and the PD-1/PD-L1 axis[149-152]. Additionally, anti-TGF-β was shown to act in synergy with ICB by suppressing immunosuppressive Tregs and EMT in cancer cells in a murine squamous cell carcinoma (SCC) model. However, not all tumor models respond equally well to the combination since its efficacy seems to be highly dependent on CTL anti-tumor activity, suggesting that the most immunogenic tumors are expected to benefit the most from this combination.
TGF-β-targeting therapies in combination clinical trials with ICB for advanced solid cancers include the small molecule tyrosine kinase inhibitors (TKIs) vactosertib and LY3200882, which specifically target TGF-βRI signaling via ALK5 inhibition (NCT04158700, NCT04064190, NCT02937272). The most advanced of these, galunisertib, has been shown to inhibit in vivo cancer cell invasion and metastasis in addition to the mechanisms mentioned above; however, it also inhibits p38α due to its similarity to ALK5, and this may contribute to potentially serious side effects that have caused other TKIs in this class of drugs to fail. It was recently announced that Eli Lilly discontinued the development of galusertinib. However, several alternative TGF-β-targeting strategies are also being tested in the clinic, including AVID200, a novel fusion protein that specifically traps free TGF-β1/3 and has recently shown promising safety in a phase I monotherapy trial, and bintrafusp-alfa (formerly M7824), an anti-PD-L1/TGF-βRII fusion protein that functions both as a checkpoint inhibitor and a TIME-localized TGF-β trap. Bintrafusp alfa has shown superior efficacy in several murine models compared to anti-PD-L1 and anti-TGF-β administered both alone and in combination while also reversing TGF-β1-induced tumor cell plasticity, prompting multiple clinical trials in various malignancies including lung (NSCLC and SCLC), breast, cervical, and colorectal (CRC) cancers as monotherapy or in combination with radio- or chemotherapy (NCT02517398, NCT03554473, NCT03620201, NCT03524170, NCT03579472, NCT04246489, NCT03436563). Notable among these is the trial in second-line advanced NSCLC (unselected for PD-L1 expression level), which has shown durable responses and encouraging long-term survival while maintaining a manageable safety profile over a two-year follow-up period, prompting a randomized phase III clinical trial vs. pembrolizumab in first-line PD-L1-high NSCLC (NCT03631706).
AXL receptor tyrosine kinase (RTK) has been consistently linked to EMT-mediated drug resistance in a number of cancers, and thus represents a promising drug target in this context. AXL expression is prevalent in EMT- and stem cell-related gene expression profiles, highlighting its role in facilitating plasticity phenotypes[95,158-160]. AXL signaling has also been shown to contribute uniquely to both tumor intrinsic and microenvironmental immunosuppression and is initiated by its ligand Gas6 as well as heterodimerization with other RTKs. Antony and colleagues showed that GAS6-AXL signaling network is a mesenchymal molecular subtype-specific therapeutic target in ovarian cancer. Of note, this paper also elegantly demonstrated the crucial role of AXL moving from cholesterol-rich lipid rafts in epithelial carcinoma cells to the normal plasma membrane domain where it multimerizes with other RTKs in mesenchymal carcinoma cells. In a later study, Antony and co-authors were able to demonstrate that the tumor suppressor opioid-binding protein/cell adhesion molecule (OPCML), which is silenced in over 83% of ovarian carcinomas by loss of heterozygosity or by epigenetic mechanisms, is spatially restricted to the cholesterol-rich lipid rafts together with AXL, and when present, represses AXL-dependent oncogenic signaling through protein tyrosine phosphatase receptor type G (PTPRG) in a coordinated manner. This study also serves to illustrate how two spatially restricted tumor suppressors, OPCML and PTPRG, coordinate to repress AXL-dependent oncogenic signaling in the Epi context, and where the loss of lipid raft organization upon EMT could lead to overactivation of AXL and more promiscuous heterodimerization with other RTKs in the M state. Thus, a therapeutic strategy to re-introduce OPCML represents an opportunity to target signaling networks, as opposed to more linear systems. AXL signaling activates downstream MAPK/ERK and PI3K/Akt pathways, which are known to drive cell survival, proliferation, migration and invasion, both of which are crucial for cancer progression and associated with poor patient outcomes[157,163]. AXL inhibition in malignant tumors holds the potential to target AXL-mediated epithelial plasticity, stimulate antigen presentation, and block the recruitment of immunosuppressive macrophages to the TIME[164,165]. As such, several AXL-targeting therapeutics have emerged and are in various phases of clinical development in combination with ICB. Although not initially developed as AXL-targeting agents, pan-TKIs that inhibit a spectrum of RTKs including AXL, most notably cabozantinib and sitravatinib, have shown promising activity in combination with ICB particularly in ICB-naïve renal cell carcinoma (NCT03937219, NCT03680521). The most advanced clinical stage selective small molecule AXL kinase inhibitor is bemcentinib (BGB324, formerly R428)[159,166]. Bemcentinib is currently in phase II development for a variety of malignancies including NSCLC (NCT03184571), mesothelioma (NCT03654833), triple-negative breast cancer (NCT03184558), and melanoma (NCT02872259) in combination with pembrolizumab. A recent presentation of results from an ICB-naive, advanced NSCLC cohort treated with bemcentinib and pembrolizumab (NCT03184571) reported improved overall response and disease control rates with a promising safety profile compared to previous benchmarks of pembrolizumab monotherapy and salvage chemotherapy. Strikingly, transcriptional analysis showed that pretreatment tumor biopsy samples from patients who turned out to be durable responders to the combination treatment displayed significant upregulation of EMT and myeloid activation gene expression signatures including AXL and TGFB1. In contrast, a negative regulation of EMT gene signature was downregulated; notably, PD-L1 and INFG levels were not associated with response. Importantly, over half the patients in the cohort were also PD-L1 negative (< 1% tumor positive cells) as assessed by IHC staining of pretreatment biopsies, although the particular assay does not account for PD-L1 expression in immune cells which may play a significant role. By the same token, stratification of patients based on AXL IHC staining of both tumor and immune cells was associated with significantly improved patient survival. In addition to enhancing responses to non-inflamed (PD-L1-low) tumors, EMT targeting is currently being pursued as a strategy to restore the efficacy of ICB by rechallenging ICB-refractory patients with EMT-ICB combination therapies. In NSCLC, ICB-refractory patients are increasingly treated with salvage chemotherapy, as prior ICB regimens appear to have a chemo-sensitization effect. However, reversing the acquired ICB resistance may have an even more desirable effect. Phase II ICB combination trials of both bemcentinib (NCT03184571) and sitravatinib (NCT02954991) in ICB-refractory NSCLC have shown promising results compared to salvage chemotherapy benchmarks, and have allowed the advancement of sitravatinib to a phase III randomized trial vs. docetaxel (NCT03906071) and also to a phase II trial in ICB-refractory urothelial carcinoma (NCT03606174).
Members of the TAM family of RTKs (TYRO3, AXL and MER) have emerged as attractive targets for cancer therapy, and they have received a great deal of attention for ICB combination due to their suppressive functions in innate immune cells[19,170]. Thus, TAM receptor inhibition is expected to unleash an innate-driven antitumor immune response; however, blocking all three family members is expected to yield intolerable side-effects. Thus, specific inhibitors targeting one family member only are most advanced in clinical testing. Selectively targeting only MERTK is also expected to have ambiguous effects; in addition to expression on a myriad innate immune cells MERTK has also emerged as a T-cell costimulatory molecule. Thus, targeting MERTK in the TIME is expected to negatively affect T cell functionality, rendering PD-1 therapy counter-productive. Targeting the other family members AXL or TYRO3 with specific inhibitors is expected to yield a primarily antitumor immunological effect as these receptors predominantly function as immune-inhibitory receptors on APCs.
Accordingly, it is important to stress that targeting a given pathway may affect several of the innate or acquired resistance mechanisms mentioned in the previous sections due to the concerted upregulation of the pathway in multiple compartments of the TIME and the diverse yet coordinated functions that this conserved biological program engages; thus, the observed effect when combining targeted therapies with ICB in a given patient population may also be driven by one or more uncharacterized mechanisms of action. Using AXL targeting as an example, apart from its expression on subpopulations of mesenchymal cancer cells, AXL is also present on a number of immune cell types, particularly myeloid-derived suppressor cells and M2 polarized macrophages, where it confers an immunosuppressive role in tumor and normal inflammatory environments[163,170]. AXL expressing DCs were shown to display phenotypic and functional diversity, and this population of cells was suggested to represent in situ plasticity of the plasmacytoid dendritic cell lineage. Recently, an AXL+ regulatory DC population that strongly suppresses antitumor immunity was characterized. AXL is a well-established negative-feedback regulator of the innate immune response by dampening the TLR response, and as AXL inhibition has been shown to elicit an immunogenic form of cell death in cancer cells, it is expected to initiate a strong innate anticancer immune response through recruitment and activation of APCs[53,124,170]. Furthermore, inhibiting AXL has significant anti-angiogenic potential which may normalize the tumor vasculature, reduce hypoxia and play a role in reversing ICB resistance; not only does AXL signaling blockade in tumor cells decrease secretion of pro-angiogenic factors, but it also directly impairs vascular endothelial growth factor A-dependent angiogenesis in vessel endothelial cells, which ubiquitously express AXL.
From in vitro models and preclinical in vivo models, targeting EMP has emerged as one of the most promising strategies to increase both the response rates and duration of responses to ICB. Since most novel EMP-targeting drugs are currently in early phases of clinical development, it follows that these therapies must first be tested on patients who have failed currently approved standard-of-care treatments, which in many cases include ICB. Reversal, rather than prevention, of EMP is therefore being tested in most current clinical trials [Table 1], although for most compounds, the optimal strategy would be to move from second-line combination testing to 1st line combination with ICB. In the long term, based on preclinical evidence that EMP targeting might also enhance natural cancer immunosurveillance in a cancer preventive setting, it would be of great interest to also evaluate the efficacy of several drug candidates mentioned above in Table 1 in chemoprevention. In the chemopreventive context specifically, it will be important to monitor potentially toxic long-term effects, as the targeted pathways are expected to also affect both the immune and stem/progenitor cell populations necessary for maintaining physiological homeostasis and repair processes.
Most of the genomic studies thus far have relied solely on analyses of pretreatment samples, and thus the results obtained provide a brief snapshot that may be useful to dissect the hallmarks of innate resistance vs. response, whereas longitudinal sampling would provide deeper insight into the cellular heterogeneity and dynamics of acquired therapy resistance and associated intercellular communication. This information is crucial to determine which targets of EMP modulators induce optimal antitumor responses in combination with ICB in a particular context. The sum of the alterations induced in the variety of cellular populations in the TIME eventually constitutes the clinical benefit of these combination regimens. Several clinical scenarios as explained above could benefit from a rational combination strategy including EMP inhibitors [Table 1], and biomarker- or biosignature-driven clinical trial design is also expected to contribute more effectively to our biological understanding. Clearly, targeting EMP impacts the dynamic and fine-tuned regulation of the myriad cellular compartments differently. Although not covered in depth in this review, phenotypic and functional plasticity of immune cells are also expected to be affected by interventions targeting cancer EMP and contribute to clinical benefit. Much is yet to be learned regarding how EMP targeting might shift the polarization of immune cell phenotypes in a manner that either supports or represses antitumor immunity. High-dimensional single cell technologies are expected to shed light on these important questions regarding the spatial and temporal regulation of EMP in the TIME. The complex intercellular communication within the TIME, although much remains unknown, holds significant promise; increased knowledge regarding this intricate interplay may enable the coordinated polarization of cancer and immune cells in the TIME to be effectively targeted through EMP in a tailored and therapeutic fashion to improve the efficacy of cancer ICB combination therapies.
The authors wish to thank special issue editor Prof. Gerhard Hamilton and the expert referees for constructive and insightful feedback. The excellent editorial assistance of Ms. Susan Song, Ms. Chloe Yang and Ms. Lori Kang is greatly appreciated. The illustrations were created with BioRender.com.Authors’ contributions
Drafted the manuscript: Lotsberg ML, Rayford A, Engelsen AST
Contributed with their expertise in the field, with literature review, data interpretation and ideation, critically revised the manuscript: Lotsberg ML, Rayford A, Thiery JP, Belleggia G, Peters SDM, Lorens JB, Chouaib S, Terry S, Engelsen ASTAvailability of data and materials
Not applicable.Financial support and sponsorship
This work was partly supported by the Research Council of Norway through its Centres of Excellence funding scheme, project number 223250 (CCBIO affiliates). Lorens JB was supported by grants from the Norwegian Research Council (grant number 240130), and Norwegian Cancer Society (grant number 190330). Engelsen AST was supported by the FRIPRO Mobility Grant Fellowship from the Research Council of Norway co-funded by the EU’s 7th Framework Programme’s Marie Skłodowska Curie Actions (MSCA COFUND, grant agreement number 608695). Support from Legat for Forskning av Kreftsykdommer fund at UIB and the Familien Blix fund to ASTE for this project is greatly appreciated.Conflicts of interest
Rayford A is an industrial PhD candidate at University of Bergen co-funded by BerGenBio ASA and the Research Council of Norway’s industrial PhD scheme. Thiery JP is scientific founder and CSO of Biocheetah Pte Ltd Singapore and consultant/shareholder Biosyngen Pte Lte Limited and ACTgenomics Taipei Taiwan. Lorens JB is founder and shareholder of BerGenBio ASA. The remaining authors declared no conflicts of interest.Ethical approval and consent to participate
Not applicable.Consent for publication
© The Author(s) 2020.
1. Virchow R. Cellular pathology. As based upon physiological and pathological histology. Lecture XVI--Atheromatous affection of arteries. 1858. Nutr Rev 1989;47:23-5.DOIPubMed
2. Korniluk A, Koper O, Kemona H, Dymicka-Piekarska V. From inflammation to cancer. Ir J Med Sci 2017;186:57-62.DOIPubMedPMC
3. Balkwill F, Mantovani A. Inflammation and cancer: back to Virchow? Lancet 2001;357:539-45.DOIPubMed
4. Thun MJ, Henley SJ, Gansler T. Inflammation and cancer: an epidemiological perspective. In: Chadwick DJ, Goode JA, editors. Cancer and inflammation: novartis foundation symposium 256. Chichester, UK: John Wiley & Sons, Ltd; 2004. pp. 6-28.PubMed
5. Hanahan D, Weinberg RA. The hallmarks of cancer. Cell 2000;100:57-70.DOIPubMed
6. Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell 2011;144:646-74.DOIPubMed
7. Ehrlich P. Über den jetzigen Stand der Chemotherapie. Ber Dtsch Chem Ges 1909;42:17-47.DOI
8. Burnet FM. The concept of immunological surveillance. Prog Exp Tumor Res 1970;13:1-27.DOIPubMed
9. Dunn GP, Bruce AT, Ikeda H, Old LJ, Schreiber RD. Cancer immunoediting: from immunosurveillance to tumor escape. Nat Immunol 2002;3:991-8.DOIPubMed
10. Burnet M. Cancer; a biological approach. I. The processes of control. Br Med J 1957;1:779-86.DOIPubMedPMC
11. Ribatti D. The concept of immune surveillance against tumors. The first theories. Oncotarget 2017;8:7175-80.DOIPubMedPMC
12. Shankaran V, Ikeda H, Bruce AT, White JM, Swanson PE, et al. IFNgamma and lymphocytes prevent primary tumour development and shape tumour immunogenicity. Nature 2001;410:1107-11.DOIPubMed
13. Schreiber RD, Old LJ, Smyth MJ. Cancer immunoediting: integrating immunity’s roles in cancer suppression and promotion. Science 2011;331:1565-70.DOIPubMed
14. Alexandrov LB, Nik-Zainal S, Wedge DC, Aparicio SAJR, Behjati S, et al. Signatures of mutational processes in human cancer. Nature 2013;500:415-21.DOIPubMedPMC
15. Rizvi NA, Hellmann MD, Snyder A, Kvistborg P, Makarov V, et al. Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer. Science 2015;348:124-8.DOIPubMedPMC
16. Furuya-Kanamori L, Bell KJL, Clark J, Glasziou P, Doi SAR. Prevalence of differentiated thyroid cancer in autopsy studies over six decades: a meta-analysis. J Clin Oncol 2016;34:3672-9.DOIPubMed
17. Coley WB. The treatment of malignant tumors by repeated inoculations of erysipelas. With a report of ten original cases. 1893. Clin Orthop Relat Res 1991:3-11.PubMed
18. Coley WB. The treatment of inoperable sarcoma by bacterial toxins (the mixed toxins of the streptococcus erysipelas and the bacillus prodigiosus). Proc R Soc Med 1910;3:1-48.PubMedPMC
19. Kamat AM, Hahn NM, Efstathiou JA, Lerner SP, Malmström PU, et al. Bladder cancer. Lancet 2016;388:2796-810.DOIPubMed
20. Knowles MA, Hurst CD. Molecular biology of bladder cancer: new insights into pathogenesis and clinical diversity. Nat Rev Cancer 2015;15:25-41.DOIPubMed
21. Krummel MF, Allison JP. CD28 and CTLA-4 have opposing effects on the response of T cells to stimulation. J Exp Med 1995;182:459-65.DOIPubMedPMC
22. Leach DR, Krummel MF, Allison JP. Enhancement of antitumor immunity by CTLA-4 blockade. Science 1996;271:1734-6.DOIPubMed
23. Hodi FS, O’Day SJ, McDermott DF, Weber RW, Sosman JA, et al. Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med 2010;363:711-23.DOIPubMedPMC
24. Ishida Y, Agata Y, Shibahara K, Honjo T. Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death. EMBO J 1992;11:3887-95.PubMedPMC
25. Dong H, Zhu G, Tamada K, Chen L. B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion. Nat Med 1999;5:1365-9.DOIPubMed
26. Freeman GJ, Long AJ, Iwai Y, Bourque K, Chernova T, et al. Engagement of the PD-1 immunoinhibitory receptor by a novel B7 family member leads to negative regulation of lymphocyte activation. J Exp Med 2000;192:1027-34.DOIPubMedPMC
27. Iwai Y, Ishida M, Tanaka Y, Okazaki T, Honjo T, et al. Involvement of PD-L1 on tumor cells in the escape from host immune system and tumor immunotherapy by PD-L1 blockade. Proc Natl Acad Sci USA 2002;99:12293-7.DOIPubMedPMC
28. Xiang X, Yu PC, Long D, Liao XL, Zhang S, et al. Prognostic value of PD -L1 expression in patients with primary solid tumors. Oncotarget 2018;9:5058-72.DOIPubMedPMC
29. Carlsson J, Sundqvist P, Kosuta V, Fält A, Giunchi F, et al. PD-L1 expression is associated with poor prognosis in renal cell carcinoma. Appl Immunohistochem Mol Morphol 2020;28:213-20.DOIPubMed
30. de Vicente JC, Rodríguez-Santamarta T, Rodrigo JP, Blanco-Lorenzo V, Allonca E, et al. PD-L1 expression in tumor cells is an independent unfavorable prognostic factor in oral squamous cell carcinoma. Cancer Epidemiol Biomarkers Prev 2019;28:546-54.DOIPubMed
31. Massi D, Brusa D, Merelli B, Falcone C, Xue G, et al. The status of PD-L1 and tumor-infiltrating immune cells predict resistance and poor prognosis in BRAFi-treated melanoma patients harboring mutant BRAFV600. Ann Oncol 2015;26:1980-7.DOIPubMed
32. Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med 2012;366:2443-54.DOIPubMedPMC
33. Borghaei H, Paz-Ares L, Horn L, Spigel DR, Steins M, et al. Nivolumab versus docetaxel in advanced nonsquamous non-small-cell lung cancer. N Engl J Med 2015;373:1627-39.DOIPubMedPMC
34. Brahmer J, Reckamp KL, Baas P, Crinò L, Eberhardt WE, et al. Nivolumab versus docetaxel in advanced squamous-cell non-small-cell lung cancer. N Engl J Med 2015;373:123-35.DOIPubMedPMC
35. Powles T, O’Donnell PH, Massard C, Arkenau HT, Friedlander TW, et al. Efficacy and safety of durvalumab in locally advanced or metastatic urothelial carcinoma: updated results from a phase 1/2 open-label study. JAMA Oncol 2017;3:e172411.DOIPubMedPMC
36. Three drugs approved for urothelial carcinoma by FDA. Cancer Discov 2017;7:659-60.DOIPubMed
37. Sharma P, Hu-Lieskovan S, Wargo JA, Ribas A. Primary, adaptive, and acquired resistance to cancer immunotherapy. Cell 2017;168:707-23.DOIPubMedPMC
38. Hellmann MD, Rizvi NA, Goldman JW, Gettinger SN, Borghaei H, et al. Nivolumab plus ipilimumab as first-line treatment for advanced non-small-cell lung cancer (CheckMate 012): results of an open-label, phase 1, multicohort study. Lancet Oncol 2017;18:31-41.DOIPubMedPMC
39. Motzer RJ, Rini BI, McDermott DF, Redman BG, Kuzel TM, et al. Nivolumab for metastatic renal cell carcinoma: results of a randomized phase II trial. J Clin Oncol 2015;33:1430-7.DOIPubMedPMC
40. Hargadon KM, Johnson CE, Williams CJ. Immune checkpoint blockade therapy for cancer: an overview of FDA-approved immune checkpoint inhibitors. Int Immunopharmacol 2018;62:29-39.DOIPubMed
41. Syed YY. Durvalumab: first global approval. Drugs 2017;77:1369-76.DOIPubMedPMC
42. Nishino M, Ramaiya NH, Hatabu H, Hodi FS. Monitoring immune-checkpoint blockade: response evaluation and biomarker development. Nat Rev Clin Oncol 2017;14:655-68.DOIPubMedPMC
43. Schadendorf D, Hodi FS, Robert C, Weber JS, Margolin K, et al. Pooled analysis of long-term survival data from phase II and phase III trials of ipilimumab in unresectable or metastatic melanoma. J Clin Oncol 2015;33:1889-94.DOIPubMedPMC
44. Trotta AM, Pacelli R, Scala S. Predictive immune biomarkers: an unattainable chimera? Cell Mol Immunol 2018;15:740-2.DOIPubMedPMC
45. Syn NL, Teng MWL, Mok TSK, Soo RA. De-novo and acquired resistance to immune checkpoint targeting. Lancet Oncol 2017;18:e731-41.DOIPubMed
46. Garzón-Orjuela N, Prieto-Pinto L, Lasalvia P, Herrera D, Castrillón J, et al. Efficacy and safety of dabrafenib-trametinib in the treatment of unresectable advanced/metastatic melanoma with BRAF-V600 mutation: a systematic review and network meta-analysis. Dermatol Ther 2020;33:e13145.DOIPubMed
47. Tray N, Weber JS, Adams S. Predictive biomarkers for checkpoint immunotherapy: current status and challenges for clinical application. Cancer Immunol Res 2018;6:1122-8.DOIPubMed
48. Schumacher TN, Schreiber RD. Neoantigens in cancer immunotherapy. Science 2015;348:69-74.DOIPubMed
49. Galon J, Bruni D. Approaches to treat immune hot, altered and cold tumours with combination immunotherapies. Nat Rev Drug Discov 2019;18:197-218.DOIPubMed
50. Snyder A, Makarov V, Merghoub T, Yuan J, Zaretsky JM, et al. Genetic basis for clinical response to CTLA-4 blockade in melanoma. N Engl J Med 2014;371:2189-99.DOIPubMedPMC
51. Van Allen EM, Miao D, Schilling B, Shukla SA, Blank C, et al. Genomic correlates of response to CTLA-4 blockade in metastatic melanoma. Science 2015;350:207-11.DOIPubMedPMC
52. Chan TA, Yarchoan M, Jaffee E, Swanton C, Quezada SA, et al. Development of tumor mutation burden as an immunotherapy biomarker: utility for the oncology clinic. Ann Oncol 2019;30:44-56.DOIPubMedPMC
53. Lotsberg ML, Chen S, Dhakal S, Lorens JB, Baguley B, et al. Autophagy mediated danger signaling regulates tumor immunosurveillance and may potentiate the effects of anti-cancer immunotherapy through increased adjuvanticity. Autophagy in immune response: impact on cancer immunotherapy. Elsevier; 2020. pp. 119-40.
54. Klymkowsky MW, Savagner P. Epithelial-mesenchymal transition: a cancer researcher’s conceptual friend and foe. Am J Pathol 2009;174:1588-93.DOIPubMedPMC
55. Hay ED. An overview of epithelio-mesenchymal transformation. Acta Anat (Basel) 1995;154:8-20.DOIPubMed
56. Greenburg G, Hay ED. Epithelia suspended in collagen gels can lose polarity and express characteristics of migrating mesenchymal cells. J Cell Biol 1982;95:333-9.DOIPubMedPMC
57. Hay ED. Organization and fine structure of epithelium and mesenchyme in the developing chick embryo. Biology 1968.
58. Kalluri R, Weinberg RA. The basics of epithelial-mesenchymal transition. J Clin Invest 2009;119:1420-8.DOIPubMedPMC
59. Davis FM, Stewart TA, Thompson EW, Monteith GR. Targeting EMT in cancer: opportunities for pharmacological intervention. Trends Pharmacol Sci 2014;35:479-88.DOIPubMed
60. Zhang Y, Weinberg RA. Epithelial-to-mesenchymal transition in cancer: complexity and opportunities. Front Med 2018;12:361-73.DOIPubMedPMC
61. Nieto MA, Huang RYJ, Jackson RA, Thiery JP. EMT: 2016. Cell 2016;166:21-45.DOIPubMed
62. Yang J, Antin P, Berx G, Blanpain C, Brabletz T, et al. Guidelines and definitions for research on epithelial-mesenchymal transition. Nat Rev Mol Cell Biol 2020;21:341-52.DOIPubMedPMC
63. Thiery JP. Epithelial-mesenchymal transitions in tumour progression. Nat Rev Cancer 2002;2:442-54.DOIPubMed
64. Nieto MA. The ins and outs of the epithelial to mesenchymal transition in health and disease. Annu Rev Cell Dev Biol 2011;27:347-76.DOIPubMed
65. Sistigu A, Di Modugno F, Manic G, Nisticò P. Deciphering the loop of epithelial-mesenchymal transition, inflammatory cytokines and cancer immunoediting. Cytokine Growth Factor Rev 2017;36:67-77.DOIPubMed
66. Nisticò P, Bissell MJ, Radisky DC. Epithelial-mesenchymal transition: general principles and pathological relevance with special emphasis on the role of matrix metalloproteinases. Cold Spring Harb Perspect Biol 2012;4.DOIPubMedPMC
67. Martin M, Wei H, Lu T. Targeting microenvironment in cancer therapeutics. Oncotarget 2016;7:52575-83.DOIPubMedPMC
68. Hugo H, Ackland ML, Blick T, Lawrence MG, Clements JA, et al. Epithelial--mesenchymal and mesenchymal--epithelial transitions in carcinoma progression. J Cell Physiol 2007;213:374-83.DOIPubMed
69. Tan TZ, Miow QH, Miki Y, Noda T, Mori S, et al. Epithelial-mesenchymal transition spectrum quantification and its efficacy in deciphering survival and drug responses of cancer patients. EMBO Mol Med 2014;6:1279-93.DOIPubMedPMC
70. Burger GA, Danen EHJ, Beltman JB. Deciphering epithelial-mesenchymal transition regulatory networks in cancer through computational approaches. Front Oncol 2017;7:162.DOIPubMedPMC
71. Thiery JP, Acloque H, Huang RYJ, Nieto MA. Epithelial-mesenchymal transitions in development and disease. Cell 2009;139:871-90.DOIPubMed
72. Li FZ, Dhillon AS, Anderson RL, McArthur G, Ferrao PT. Phenotype switching in melanoma: implications for progression and therapy. Front Oncol 2015;5:31.DOIPubMedPMC
73. Caramel J, Papadogeorgakis E, Hill L, Browne GJ, Richard G, et al. A switch in the expression of embryonic EMT-inducers drives the development of malignant melanoma. Cancer Cell 2013;24:466-80.DOIPubMed
74. Richard G, Dalle S, Monet MA, Ligier M, Boespflug A, et al. ZEB1-mediated melanoma cell plasticity enhances resistance to MAPK inhibitors. EMBO Mol Med 2016;8:1143-61.DOIPubMedPMC
75. Williams ED, Gao D, Redfern A, Thompson EW. Controversies around epithelial-mesenchymal plasticity in cancer metastasis. Nat Rev Cancer 2019;19:716-32.DOIPubMedPMC
76. Pastushenko I, Brisebarre A, Sifrim A, Fioramonti M, Revenco T, et al. Identification of the tumour transition states occurring during EMT. Nature 2018;556:463-8.DOIPubMed
77. Gupta PB, Pastushenko I, Skibinski A, Blanpain C, Kuperwasser C. Phenotypic plasticity: driver of cancer initiation, progression, and therapy resistance. Cell Stem Cell 2019;24:65-78.DOIPubMedPMC
78. Boumahdi S, de Sauvage FJ. The great escape: tumour cell plasticity in resistance to targeted therapy. Nat Rev Drug Discov 2020;19:39-56.DOIPubMed
79. Ramirez M, Rajaram S, Steininger RJ, Osipchuk D, Roth MA, et al. Diverse drug-resistance mechanisms can emerge from drug-tolerant cancer persister cells. Nat Commun 2016;7:10690.DOIPubMedPMC
80. Sharma SV, Lee DY, Li B, Quinlan MP, Takahashi F, et al. A chromatin-mediated reversible drug-tolerant state in cancer cell subpopulations. Cell 2010;141:69-80.DOIPubMedPMC
81. Røsland GV, Engelsen AST. Novel points of attack for targeted cancer therapy. Basic Clin Pharmacol Toxicol 2015;116:9-18.DOIPubMedPMC
82. Recondo G, Mezquita L, Facchinetti F, Planchard D, Gazzah A, et al. Diverse resistance mechanisms to the third-generation ALK inhibitor lorlatinib in ALK-rearranged lung cancer. Clin Cancer Res 2020;26:242-55.DOIPubMedPMC
83. Shibue T, Weinberg RA. EMT, CSCs, and drug resistance: the mechanistic link and clinical implications. Nat Rev Clin Oncol 2017;14:611-29.DOIPubMedPMC
84. Mani SA, Guo W, Liao MJ, Eaton EN, Ayyanan A, et al. The epithelial-mesenchymal transition generates cells with properties of stem cells. Cell 2008;133:704-15.DOIPubMedPMC
85. Guo W, Keckesova Z, Donaher JL, Shibue T, Tischler V, et al. Slug and Sox9 cooperatively determine the mammary stem cell state. Cell 2012;148:1015-28.DOIPubMedPMC
86. Talbot LJ, Bhattacharya SD, Kuo PC. Epithelial-mesenchymal transition, the tumor microenvironment, and metastatic behavior of epithelial malignancies. Int J Biochem Mol Biol 2012;3:117-36.PubMedPMC
87. Ocaña OH, Córcoles R, Fabra A, Moreno-Bueno G, Acloque H, et al. Metastatic colonization requires the repression of the epithelial-mesenchymal transition inducer Prrx1. Cancer Cell 2012;22:709-24.DOIPubMed
88. Touil Y, Igoudjil W, Corvaisier M, Dessein AF, Vandomme J, et al. Colon cancer cells escape 5FU chemotherapy-induced cell death by entering stemness and quiescence associated with the c-Yes/YAP axis. Clin Cancer Res 2014;20:837-46.DOIPubMedPMC
89. Liau BB, Sievers C, Donohue LK, Gillespie SM, Flavahan WA, et al. Adaptive chromatin remodeling drives glioblastoma stem cell plasticity and drug tolerance. Cell Stem Cell 2017;20:233-46.e7.DOIPubMedPMC
90. Hata AN, Niederst MJ, Archibald HL, Gomez-Caraballo M, Siddiqui FM, et al. Tumor cells can follow distinct evolutionary paths to become resistant to epidermal growth factor receptor inhibition. Nat Med 2016;22:262-9.DOIPubMedPMC
91. Shaffer SM, Dunagin MC, Torborg SR, Torre EA, Emert B, et al. Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance. Nature 2017;546:431-5.DOIPubMedPMC
92. Müller J, Krijgsman O, Tsoi J, Robert L, Hugo W, et al. Low MITF/AXL ratio predicts early resistance to multiple targeted drugs in melanoma. Nat Commun 2014;5:5712.DOIPubMedPMC
93. Hoek KS, Eichhoff OM, Schlegel NC, Döbbeling U, Kobert N, et al. In vivo switching of human melanoma cells between proliferative and invasive states. Cancer Res 2008;68:650-6.DOIPubMed
94. Konieczkowski DJ, Johannessen CM, Abudayyeh O, Kim JW, Cooper ZA, et al. A melanoma cell state distinction influences sensitivity to MAPK pathway inhibitors. Cancer Discov 2014;4:816-27.DOIPubMedPMC
95. Tirosh I, Izar B, Prakadan SM, Wadsworth MH, Treacy D, et al. Dissecting the multicellular ecosystem of metastatic melanoma by single-cell RNA-seq. Science 2016;352:189-96.DOIPubMedPMC
96. Terry S, Buart S, Tan TZ, Gros G, Noman MZ, et al. Acquisition of tumor cell phenotypic diversity along the EMT spectrum under hypoxic pressure: consequences on susceptibility to cell-mediated cytotoxicity. Oncoimmunology 2017;6:e1271858.DOIPubMedPMC
97. Bhowmick NA, Ghiassi M, Bakin A, Aakre M, Lundquist CA, et al. Transforming growth factor-beta1 mediates epithelial to mesenchymal transdifferentiation through a RhoA-dependent mechanism. Mol Biol Cell 2001;12:27-36.DOIPubMedPMC
98. Jokela TA, Engelsen AST, Rybicka A, Pelissier Vatter FA, Garbe JC, et al. Microenvironment-induced non-sporadic expression of the AXL and cKIT receptors are related to epithelial plasticity and drug resistance. Front Cell Dev Biol 2018;6:41.DOIPubMedPMC
99. Terry S, Faouzi Zaarour R, Hassan Venkatesh G, Francis A, et al. Role of hypoxic stress in regulating tumor immunogenicity, resistance and plasticity. Int J Mol Sci 2018;19.DOIPubMedPMC
100. Hasmim M, Noman MZ, Messai Y, Bordereaux D, Gros G, et al. Cutting edge: hypoxia-induced nanog favors the intratumoral infiltration of regulatory T cells and macrophages via direct regulation of TGF-β1. J Immunol 2013;191:5802-6.DOIPubMed
101. Noman MZ, Benlalam H, Hasmim M, Chouaib S. Cytotoxic T cells - stroma interactions. Bull Cancer 2011;98:E19-24.DOIPubMed
102. Noman MZ, Chouaib S. Targeting hypoxia at the forefront of anticancer immune responses. Oncoimmunology 2014;3:e954463.DOIPubMedPMC
103. Noman MZ, Desantis G, Janji B, Hasmim M, Karray S, et al. PD-L1 is a novel direct target of HIF-1α, and its blockade under hypoxia enhanced MDSC-mediated T cell activation. J Exp Med 2014;211:781-90.DOIPubMedPMC
104. Noman MZ, Hasmim M, Lequeux A, Xiao M, Duhem C, et al. Improving cancer immunotherapy by targeting the hypoxic tumor microenvironment: new opportunities and challenges. Cells 2019;8.DOIPubMedPMC
105. Chouaib S, Noman MZ, Kosmatopoulos K, Curran MA. Hypoxic stress: obstacles and opportunities for innovative immunotherapy of cancer. Oncogene 2017;36:439-45.DOIPubMedPMC
106. Dong Y, Zheng Q, Wang Z, Lin X, You Y, et al. Higher matrix stiffness as an independent initiator triggers epithelial-mesenchymal transition and facilitates HCC metastasis. J Hematol Oncol 2019;12:112.DOIPubMedPMC
107. Gonzalez DM, Medici D. Signaling mechanisms of the epithelial-mesenchymal transition. Sci Signal 2014;7:re8.DOIPubMedPMC
108. Horn LA, Fousek K, Palena C. Tumor plasticity and resistance to immunotherapy. Trends Cancer 2020;6:432-41.DOIPubMedPMC
109. Fiori ME, Di Franco S, Villanova L, Bianca P, Stassi G, et al. Cancer-associated fibroblasts as abettors of tumor progression at the crossroads of EMT and therapy resistance. Mol Cancer 2019;18:70.DOIPubMedPMC
110. Huergo-Zapico L, Parodi M, Cantoni C, Lavarello C, Fernández-Martínez JL, et al. NK-cell editing mediates epithelial-to-mesenchymal transition via phenotypic and proteomic changes in melanoma cell lines. Cancer Res 2018;78:3913-25.DOIPubMed
111. Romeo E, Caserta CA, Rumio C, Marcucci F. The vicious cross-talk between tumor cells with an EMT phenotype and cells of the immune system. Cells 2019;8.DOIPubMedPMC
112. Wu Y, Deng J, Rychahou PG, Qiu S, Evers BM, et al. Stabilization of snail by NF-kappaB is required for inflammation-induced cell migration and invasion. Cancer Cell 2009;15:416-28.DOIPubMedPMC
113. Bonde A-K, Tischler V, Kumar S, Soltermann A, Schwendener RA. Intratumoral macrophages contribute to epithelial-mesenchymal transition in solid tumors. BMC Cancer 2012;12:35.DOIPubMedPMC
114. Toh B, Wang X, Keeble J, Sim WJ, Khoo K, et al. Mesenchymal transition and dissemination of cancer cells is driven by myeloid-derived suppressor cells infiltrating the primary tumor. PLoS Biol 2011;9:e1001162.DOIPubMedPMC
115. Glodde N, Bald T, van den Boorn-Konijnenberg D, Nakamura K, O’Donnell JS, et al. Reactive neutrophil responses dependent on the receptor tyrosine kinase c-MET limit cancer immunotherapy. Immunity 2017;47:789-802.e9.DOIPubMed
116. Li S, Cong X, Gao H, Lan X, Li Z, et al. Tumor-associated neutrophils induce EMT by IL-17α to promote migration and invasion in gastric cancer cells. J Exp Clin Cancer Res 2019;38:6.DOIPubMedPMC
117. Chen DS, Mellman I. Oncology meets immunology: the cancer-immunity cycle. Immunity 2013;39:1-10.DOIPubMed
118. Matzinger P. The danger model: a renewed sense of self. Science 2002;296:301-5.DOIPubMed
119. Garg AD, Agostinis P. Cell death and immunity in cancer: from danger signals to mimicry of pathogen defense responses. Immunol Rev 2017;280:126-48.DOIPubMed
120. Kroemer G, Galluzzi L, Kepp O, Zitvogel L. Immunogenic cell death in cancer therapy. Annu Rev Immunol 2013;31:51-72.DOIPubMed
121. Gao D. Compound-therapy based on cancer-immunity cycle: promising prospects for antitumor regimens. Am J Cancer Res 2019;9:212-8.PubMedPMC
122. Zhao T, Ren H, Jia L, Chen J, Xin W, et al. Inhibition of HIF-1α by PX-478 enhances the anti-tumor effect of gemcitabine by inducing immunogenic cell death in pancreatic ductal adenocarcinoma. Oncotarget 2015;6:2250-62.DOIPubMedPMC
123. Akalay I, Janji B, Hasmim M, Noman MZ, Thiery JP, et al. EMT impairs breast carcinoma cell susceptibility to CTL-mediated lysis through autophagy induction. Autophagy 2013;9:1104-6.DOIPubMedPMC
124. Lotsberg ML, Wnuk-Lipinska K, Terry S, Tan TZ, Lu N, et al. AXL targeting abrogates autophagic flux and induces immunogenic cell death in drug-resistant cancer cells. J Thorac Oncol 2020;15:973-99.DOIPubMedPMC
125. Kroemer G, Galluzzi L. Autophagy-dependent danger signaling and adaptive immunity to poorly immunogenic tumors. Oncotarget 2017;8:5686-91.DOIPubMedPMC
126. Aguilera TA, Rafat M, Castellini L, Shehade H, Kariolis MS, et al. Reprogramming the immunological microenvironment through radiation and targeting Axl. Nat Commun 2016;7:13898.DOIPubMedPMC
127. Terry S, Abdou A, Engelsen AST, Buart S, Dessen P, et al. AXL targeting overcomes human lung cancer cell resistance to NK- and CTL-mediated cytotoxicity. Cancer Immunol Res 2019;7:1789-802.DOIPubMed
128. Terry S, Savagner P, Ortiz-Cuaran S, Mahjoubi L, Saintigny P, et al. New insights into the role of EMT in tumor immune escape. Mol Oncol 2017;11:824-46.DOIPubMedPMC
129. Al Absi A, Wurzer H, Guerin C, Hoffmann C, Moreau F, et al. Actin cytoskeleton remodeling drives breast cancer cell escape from natural killer-mediated cytotoxicity. Cancer Res 2018;78:5631-43.DOIPubMed
130. Kudo-Saito C, Shirako H, Takeuchi T, Kawakami Y. Cancer metastasis is accelerated through immunosuppression during Snail-induced EMT of cancer cells. Cancer Cell 2009;15:195-206.DOIPubMed
131. Chouaib S, Janji B, Tittarelli A, Eggermont A, Thiery JP. Tumor plasticity interferes with anti-tumor immunity. Crit Rev Immunol 2014;34:91-102.DOIPubMed
132. Akalay I, Tan TZ, Kumar P, Janji B, Mami-Chouaib F, et al. Targeting WNT1-inducible signaling pathway protein 2 alters human breast cancer cell susceptibility to specific lysis through regulation of KLF-4 and miR-7 expression. Oncogene 2015;34:2261-71.DOIPubMed
133. Dongre A, Rashidian M, Reinhardt F, Bagnato A, Keckesova Z, et al. Epithelial-to-mesenchymal transition contributes to immunosuppression in breast carcinomas. Cancer Res 2017;77:3982-9.DOIPubMedPMC
134. Chen L, Gibbons DL, Goswami S, Cortez MA, Ahn YH, et al. Metastasis is regulated via microRNA-200/ZEB1 axis control of tumour cell PD-L1 expression and intratumoral immunosuppression. Nat Commun 2014;5:5241.DOIPubMedPMC
135. Hugo W, Zaretsky JM, Sun L, Song C, Moreno BH, et al. Genomic and transcriptomic features of response to anti-PD-1 therapy in metastatic melanoma. Cell 2016;165:35-44.DOIPubMedPMC
136. Thompson JC, Hwang WT, Davis C, Deshpande C, Jeffries S, et al. Gene signatures of tumor inflammation and epithelial-to-mesenchymal transition (EMT) predict responses to immune checkpoint blockade in lung cancer with high accuracy. Lung Cancer 2020;139:1-8.DOIPubMedPMC
137. Wang L, Saci A, Szabo PM, Chasalow SD, Castillo-Martin M, et al. EMT- and stroma-related gene expression and resistance to PD-1 blockade in urothelial cancer. Nat Commun 2018;9:3503.DOIPubMedPMC
138. Gao J, Shi LZ, Zhao H, Chen J, Xiong L, et al. Loss of IFN-γ pathway genes in tumor cells as a mechanism of resistance to anti-CTLA-4 therapy. Cell 2016;167:397-404.e9.DOIPubMedPMC
139. Shin DS, Zaretsky JM, Escuin-Ordinas H, Garcia-Diaz A, Hu-Lieskovan S, et al. Primary resistance to PD-1 blockade mediated by JAK1/2 mutations. Cancer Discov 2017;7:188-201.DOIPubMedPMC
140. Luke JJ, Bao R, Sweis RF, Spranger S, Gajewski TF. WNT/β-catenin pathway activation correlates with immune exclusion across human cancers. Clin Cancer Res 2019;25:3074-83.DOIPubMedPMC
141. Spranger S, Bao R, Gajewski TF. Melanoma-intrinsic β-catenin signalling prevents anti-tumour immunity. Nature 2015;523:231-5.DOIPubMed
142. Ruiz de Galarreta M, Bresnahan E, Molina-Sánchez P, Lindblad KE, Maier B, et al. β-catenin activation promotes immune escape and resistance to anti-PD-1 therapy in hepatocellular carcinoma. Cancer Discov 2019;9:1124-41.DOIPubMedPMC
143. Grasso CS, Giannakis M, Wells DK, Hamada T, Mu XJ, et al. Genetic mechanisms of immune evasion in colorectal cancer. Cancer Discov 2018;8:730-49.DOIPubMedPMC
144. Trujillo JA, Luke JJ, Zha Y, Segal JP, Ritterhouse LL, et al. Secondary resistance to immunotherapy associated with β-catenin pathway activation or PTEN loss in metastatic melanoma. J Immunother Cancer 2019;7:295.DOIPubMedPMC
145. Horn LA, Riskin J, Hempel HA, Fousek K, Lind H, et al. Simultaneous inhibition of CXCR1/2, TGF-β, and PD-L1 remodels the tumor and its microenvironment to drive antitumor immunity. J Immunother Cancer 2020;8.DOIPubMedPMC
146. Anandappa AJ, Wu CJ, Ott PA. Directing traffic: how to effectively drive T cells into tumors. Cancer Discov 2020;10:185-97.DOIPubMedPMC
147. Martin CJ, Datta A, Littlefield C, Kalra A, Chapron C, et al. Selective inhibition of TGFβ1 activation overcomes primary resistance to checkpoint blockade therapy by altering tumor immune landscape. Sci Transl Med 2020;12.DOIPubMed
148. Yap TA, Lakhani NJ, Araujo DV, Rodon Ahnert J, Chandana SR, et al. AVID200, first-in-class TGF-beta 1 and 3 selective and potent inhibitor: safety and biomarker results of a phase I monotherapy dose-escalation study in patients with advanced solid tumors. JCO 2020;38:3587.DOI
149. Mariathasan S, Turley SJ, Nickles D, Castiglioni A, Yuen K, et al. TGFβ attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells. Nature 2018;554:544-8.DOIPubMedPMC
150. Sow HS, Ren J, Camps M, Ossendorp F, Ten Dijke P. Combined inhibition of TGF-β signaling and the PD-L1 immune checkpoint is differentially effective in tumor models. Cells 2019;8.DOIPubMedPMC
151. Holmgaard RB, Schaer DA, Li Y, Castaneda SP, Murphy MY, et al. Targeting the TGFβ pathway with galunisertib, a TGFβRI small molecule inhibitor, promotes anti-tumor immunity leading to durable, complete responses, as monotherapy and in combination with checkpoint blockade. J Immunother Cancer 2018;6:47.DOIPubMedPMC
152. Tauriello DVF, Palomo-Ponce S, Stork D, Berenguer-Llergo A, Badia-Ramentol J, et al. TGFβ drives immune evasion in genetically reconstituted colon cancer metastasis. Nature 2018;554:538-43.DOIPubMed
153. Dodagatta-Marri E, Meyer DS, Reeves MQ, Paniagua R, To MD, et al. α-PD-1 therapy elevates Treg/Th balance and increases tumor cell pSmad3 that are both targeted by α-TGFβ antibody to promote durable rejection and immunity in squamous cell carcinomas. J Immunother Cancer 2019;7:62.DOIPubMedPMC
154. Herbertz S, Sawyer JS, Stauber AJ, Gueorguieva I, Driscoll KE, et al. Clinical development of galunisertib (LY2157299 monohydrate), a small molecule inhibitor of transforming growth factor-beta signaling pathway. Drug Des Devel Ther 2015;9:4479-99.DOIPubMedPMC
155. Xu G, Zhang Y, Wang H, Guo Z, Wang X, et al. Synthesis and biological evaluation of 4-(pyridin-4-oxy)-3-(3,3-difluorocyclobutyl)-pyrazole derivatives as novel potent transforming growth factor-β type 1 receptor inhibitors. Eur J Med Chem 2020;198:112354.DOIPubMed
156. Cho BC, Kim TM, Vicente D, Felip E, Lee DH, et al. Two-year follow-up of bintrafusp alfa, a bifunctional fusion protein targeting TGF-β and PD-L1, for second-line (2L) treatment of non-small cell lung cancer (NSCLC). JCO 2020;38:9558.DOI
157. Davidsen KT, Haaland GS, Lie MK, Lorens JB, Engelsen AST. The role of axl receptor tyrosine kinase in tumor cell plasticity and therapy resistance. In: Akslen LA, Watnick RS, editors. Biomarkers of the tumor microenvironment. Cham: Springer International Publishing; 2017. pp. 351-76.DOI
158. Kirane A, Ludwig KF, Sorrelle N, Haaland G, Sandal T, et al. Warfarin blocks Gas6-mediated axl activation required for pancreatic cancer epithelial plasticity and metastasis. Cancer Res 2015;75:3699-705.DOIPubMedPMC
159. Holland SJ, Powell MJ, Franci C, Chan EW, Friera AM, et al. Multiple roles for the receptor tyrosine kinase axl in tumor formation. Cancer Res 2005;65:9294-303.DOIPubMed
160. Taube JH, Herschkowitz JI, Komurov K, Zhou AY, Gupta S, et al. Core epithelial-to-mesenchymal transition interactome gene-expression signature is associated with claudin-low and metaplastic breast cancer subtypes. Proc Natl Acad Sci USA 2010;107:15449-54.DOIPubMedPMC
161. Antony J, Tan TZ, Kelly Z, Low J, Choolani M, et al. The GAS6-AXL signaling network is a mesenchymal (Mes) molecular subtype-specific therapeutic target for ovarian cancer. Sci Signal 2016;9:ra97.DOIPubMed
162. Antony J, Zanini E, Kelly Z, Tan TZ, Karali E, et al. The tumour suppressor OPCML promotes AXL inactivation by the phosphatase PTPRG in ovarian cancer. EMBO Rep 2018;19.DOIPubMedPMC
163. Gay CM, Balaji K, Byers LA. Giving AXL the axe: targeting AXL in human malignancy. Br J Cancer 2017;116:415-23.DOIPubMedPMC
164. Aguilera TA, Giaccia AJ. Molecular pathways: oncologic pathways and their role in T-cell exclusion and immune evasion-a new role for the AXL receptor tyrosine kinase. Clin Cancer Res 2017;23:2928-33.DOIPubMedPMC
165. Tanaka M, Siemann DW. Axl signaling is an important mediator of tumor angiogenesis. Oncotarget 2019;10:2887-98.DOIPubMedPMC
166. Sheridan C. First Axl inhibitor enters clinical trials. Nat Biotechnol 2013;31:775-6.DOIPubMed
167. Liu Y, Zugazagoitia J, Ahmed FS, Henick BS, Gettinger SN, et al. Immune cell PD-L1 colocalizes with macrophages and is associated with outcome in PD-1 pathway blockade therapy. Clin Cancer Res 2020;26:970-7.DOIPubMedPMC
168. Krebs M, Brunsvig P, Helland Å, Viñolas N, Aix S, et al. P1.01-72 a phase II study of selective AXL inhibitor bemcentinib and pembrolizumab in patients with NSCLC refractory to anti-PD(L)1. J Thorac Oncol 2019;14:S388.DOI
169. Shiono A, Kaira K, Mouri A, Yamaguchi O, Hashimoto K, et al. Improved efficacy of ramucirumab plus docetaxel after nivolumab failure in previously treated non-small cell lung cancer patients. Thorac Cancer 2019;10:775-81.DOIPubMedPMC
170. Peeters MJW, Rahbech A, Thor Straten P. TAM-ing T cells in the tumor microenvironment: implications for TAM receptor targeting. Cancer Immunol Immunother 2020;69:237-44.DOIPubMedPMC
171. Alcántara-Hernández M, Leylek R, Wagar LE, Engleman EG, Keler T, et al. High-dimensional phenotypic mapping of human dendritic cells reveals interindividual variation and tissue specialization. Immunity 2017;47:1037-50.e6.DOIPubMedPMC
172. Maier B, Leader AM, Chen ST, Tung N, Chang C, et al. A conserved dendritic-cell regulatory program limits antitumour immunity. Nature 2020;580:257-62.DOIPubMed
173. Rothlin CV, Ghosh S, Zuniga EI, Oldstone MBA, Lemke G. TAM receptors are pleiotropic inhibitors of the innate immune response. Cell 2007;131:1124-36.DOIPubMed
Lotsberg ML, Rayford A, Thiery JP, Belleggia G, D’Mello Peters S, Lorens JB, Chouaib S, Terry S, Engelsen AST. Decoding cancer’s camouflage: epithelial-mesenchymal plasticity in resistance to immune checkpoint blockade. Cancer Drug Resist 2020;3:832-853. http://dx.doi.org/10.20517/cdr.2020.41
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