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Cancer Drug Resist 2019;2:877-884.10.20517/cdr.2019.44© The Author(s) 2019.
Open AccessOriginal Article

Genetic variations in triple-negative breast cancers undergoing neo-adjuvant chemotherapy

1Department of Breast Surgical Oncology, Showa University, Shinagawaku, Tokyo 142-8666, Japan.

2Clinical Research Laboratory, Showa University, Shinagawaku, Tokyo 142-8666, Japan.

3Department of Pathology, Showa University, Shinagawaku, Tokyo 142-8666, Japan.

Correspondence Address: Dr. Miki Mori, Department of Breast Surgical Oncology, Showa University, 1-5-8 Hatanodai, Shinagawaku, Tokyo 142-8666, Japan. E-mail: wilsonmikity@yahoo.co.jp

    Science Editor: Helen M. Coley | Copy Editor: Cai-Hong Wang | Production Editor: Tian Zhang
    ...

    © The Author(s) 2019. 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.

    Abstract

    Aim: Triple negative breast cancer (TNBC) is known as aggressive subtype and have no identified targeted therapies. We examined the relationship of neoadjuvant chemotherapy response to genetic variations of TNBC.

    Methods: The tumors used in this study were collected from Showa University Hospital, Japan. Thirteen formalin-fixed paraffin-embedded tumors from Japanese TNBC patients who underwent neoadjuvant chemotherapy were used for analysis. Of these, eight surgically resected tumors showed progressive disease and/or recurrence after treatment (PD/REC), and biopsy tissues from five patients showing pathological complete response (pCR) were analyzed. DNA extracted from tissue sample were analyzed. The Miseq system and Trusight Tumor Sequence panel kit were used to sequence 174 amplicons over 82 exons of 26 cancer-related genes to identify genetic mutations.

    Results: Seven somatic non-synonymous variants were detected in three genes (FOXL2, PIK3CA, and TP53) in all five pCR patients, and six somatic non-synonymous variants in two genes (PTEN and TP53) were detected in six of eight PD/REC patients. Eight of 13 TNBC tumors were found to have TP53 pathogenic variants, in both pCR and PD/REC cases.

    Conclusion: Although TP53 variation was detected in both pCR and PD/REC cases, each location and type of the variant were different. We could not identify genetic mutations associated with chemotherapy response and recurrence.

    Introduction

    Triple-negative breast cancer (TNBC) is defined as any breast cancer lacking estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 expression. It accounts for approximately 15%-20% of all breast cancers[1,2]. TNBC is reported to behave more aggressively and is associated with a worse survival than other types of breast cancer[3,4]. Patients with TNBC have no identified targeted therapies. They are currently treated by surgery and chemotherapy alone[1].

    Triple-negative subtypes are more sensitive to neo-adjuvant chemotherapy than luminal breast cancers[5-7]. Patients with TNBC have increased pathologic complete response (pCR) rates compared with non-TNBC patients, and those with pCR have excellent survival regardless of subtype[5-7]. However, patients with progressive disease after neo-adjuvant chemotherapy have a significantly worse prognosis if they have TNBC compared with other subtypes[5,7]. About 70%-80% of patients of TNBC fail to respond to neoadjuvant chemotherapy (NAC)[5-7], but the molecular mechanism underlying differences in responders and non-responders is unclear. It is also poorly understood which genes and pathways are related to treatment response in breast tumors.

    Herein, we performed an exploratory study using next generation sequencing to investigate the dynamics of tumor gene mutations in TNBC patients receiving NAC.

    Methods

    Ethical approval

    This study was approved (number 1589) by the Institutional Review Board of Showa University, Japan. Written informed consent was received from the patients. If informed consent could not be received for the death of patients, the candidate opted out on the homepage of the hospital.

    Patient information

    The tumors analyzed in this study were collected from Showa University Hospital, Japan. Ninety four patients revealed triple negative subtype of 1111 patients of primary breast cancer surgery between 2011 and 2013. Of these 94 patients, 33 underwent neo adjuvant chemotherapy prior to surgery. Ten patients achieved pCR and remaining 23 patients had residual disease. Four patients revealed clinically progressive disease during neo adjuvant chemotherapy. Taxane followed by anthracycline based regimens were applied as standard neo-adjuvant chemotherapy. Two patients who revealed progressive disease during first taxane regimen dropped out of neo-adjuvant chemotherapy then planned surgery without following anthracycline chemotherapy. Seven patients of 23 patients who had residual disease including 3 progressive disease revealed recurrence in the same period. In total, there were 8 patients with progressive disease and/or recurrence (PD/REC). Five of 10 pCR cases underwent pretreatment biopsy in Showa University Hospital and able to obtain the sample. These 8 PD/REC cases and 5 pCR cases were analyzed. Formalin-fixed paraffin-embedded (FFPE) samples from pretreatment biopsy of PD/REC and pCR cases and surgical specimen of PD/REC cases were obtained. Clinical and pathologic information was obtained from medical chart including the information of the results of both germline BRCA1/2 testing and BRNAness. The concept of “BRCAness” is that sporadic basal-like breast cancers resemble BRCA1 mutated cancers. A set of 34 MLPA probes was used to identify BRCAness[8]. American Joint Committee on Cancer/tumor-node-metastasis cancer staging was assessed.

    Preparation of genomic DNA

    Ten slices of 10 μm-thick FFPE tissues were used for genomic DNA extraction. Tissues were de-paraffinized with xylene, then DNA was extracted using the QIAamPD/recNA FFPE Tissue Kit (Qiagen, Venlo, Netherlands) following the manufacturer’s instructions.

    Briefly, each deparaffinization solution, specific buffers and proteinase was added to destruct cells while centrifuging. After incubation, ethanol was added to precipitate DNA. After transferring the entire lysate to purification column, the centrifugation was repeated. Finally, elution buffer was added to elute DNA in the column.

    Target genes

    The TruSight Tumor Sequencing panel (Illumina, San Diego, California, USA, #FC-130-2001) was used to detect genetic variations in tumors using NGS. This panel covered 174 amplicons over 82 exons of 26 cancer-related genes. The following genes encode kinases: AKT1, ALK, BRAF, EGFR, ERBB2, FGFR2, KIT, MAP2K1, MET, PD/RECGFRA, PIK3CA, SRC, and STK11, while the remainder do not: APC, CDH1, CTNNB1, FBXW7, FOXL2, GNAQ, GNAS, KRAS, MSH6, NRAS, PTEN, SMAD4, and TP53.

    Sequencing

    The quality of the genomic DNA purified from FFPE tissues was checked by quantitative PCR using Quality Control Template (Illumina) and iQTM SYBR® Green Supermix (BioRad). Samples were required to fulfill the criteria ΔCt < 5, which was typically 30-300 ng depending on the DNA quality. However, ΔCt = 12 biopsy specimens were also included in the analysis. Genomic DNA hybridization-based enrichment was performed using the TruSight Tumor Sequence panel kit according to the manufacturer’s protocol. Pooled amplicons were end-repaired then underwent adapter ligation. The purified library was quantified using the Qubit® fluorometer with the Qubit® dsDNA BR assay kit. Finally, the captured DNA was subjected to 121-bp paired-end read sequencing on the MiSeq system (Illumina).

    Strategies for the analysis of genetic variations

    Sequence reads were exported into FASTQ format files. The alignment of pair-end sequencing reads to the reference genome was performed using a banded Smith-Waterman method with the Amplicon-DS workflow software plug-in for MiSeq Reporter. Human Genome version 19 (UCSC) was used as the alignment reference. The identification of sequencing variants was performed using the Illumina Somatic Variant Caller algorithm. The called SNPs/indels were annotated using COSMIC (somatic mutation information), the IARC TP53 database (human TP53 gene variations related to cancer)[9], and other databases of genetic variations. Database was aggregated into the Illumina VariantStudio application. Additionally, NM_000179.2:c.3254delC and NM_000179.2:c.3253_3254insC in MSH6 were eliminated as known artifact variants. Statistical analysis was performed with Fisher’s exact test.

    Results

    Clinical features of the patients

    The clinical features of the patients are summarized in the Table 1. Patients had an average age of 49.6 years. Seven cases underwent BRCA1 and BRCA2 germline mutation testing. BRCA1/2 gene testing are not covered by national healthcare insurance, so it was performed to limited patients based on age, family history by self-pay. Seven PD/REC cases, including three patients with germline mutation showed BRCAness. One pCR case also showed BRCAness.

    Table 1

    Clinical features of the patients

    pCRPD/REC
    Age, year
       Median (range)56 (40-72)46 (27-68)
    Clinical T-stage at diagnosis
       T110
       T227
       T321
       T400
    Clinical N-stage at diagnosis
       N025
       N113
       N220
       N300
    Stage at diagnosis
       I10
       II17
       III31
       IV00
    Nuclear grade
       100
       213
       344
       Not available01
    Ki-67
       < 20%00
       ≥ 20%57
       Not available01
    Histology
       Ductal48
       Lobular00
       Others10
    Subtype defined by IHC
       EGFR(+), CK5/6(+)02
       EGFR(+), CK5/6(-)01
       EGFR(-), CK5/6(+)11
       EGFR(-), CK5/6(-)23
       Not tested21
    BRCA mutation
       Deleterious03
       Negative22
       Not tested33
    BRCAness
       Yes17
       No10
       Not analyzed31
    Neo-adjuvant treatment
       Anthracycline + Taxane46
       Taxane + Other02
       Other10
    Surgery type
       Mastectomy16
       Lumpectomy42
       Sentinel Node Biopsy only24
       Axillary lymph node dissection34
    Yeild of pathological T-stage
       T050
       T104
       T203
       T301
       T400
    Yeild of pathological N-stage
       N054
       N104
       N200
       N300
    Yeild of pathological stage
       I03
       II04
       III01
       IV00
    Adjuvant treatment
       No54
       FEC01
       Gemcitabine + Carboplatin03
    Recurrence
       Yes07
       No51
    Radiation
       Yes44
       No14
    Death
       Yes03
       No55
    Average DFS (months)2517
    Average observation period (months)3440

    Genetic variations in tumors showed PD/REC and pCR

    The genetic variations after filtering out synonymous variants and known artifacts are shown in the Table 2. Three biopsy samples of 8 PD/REC cases were not available for the analysis. In PD/REC cases, we found ten non-synonymous variants were detected in the coding regions of two genes in 5 biopsy tissues before NAC, while 14 non-synonymous variants were detected in the coding regions of three genes in 8 surgical specimens after NAC. In 5 pCR cases, ten non-synonymous variants were detected in the coding regions of four genes. Of these, variants TP53 Val31Ile and Pro72Arg, STK11 Phe354Leu, and MET Asn375Ser are known polymorphisms (NIH dbSNP: rs33917957, rs1042522, rs59912467 and rs33917957, respectively).

    Table 2

    Genetic vatiations detected in pCR/PD groups

    Sample IDBiopsy samples before NACSurgical specimens after NAC
    GenePathological variationsPolymorphismsGenePathological variationsPolymorphisms
    Genetic variations in PD/REC patients
      6TP53      p.Val31IleTP53      p.Val31Ile
    TP53      p.Pro72ArgTP53      p.Pro72Arg
    STK11      p.Phe354LeuSTK11      p.Phe354Leu
      7TP53      p.Pro72ArgTP53      p.Pro72Arg
    PTEN      p.Ser179Valfs*8
      8TP53      p.Val272Met      p.Pro72ArgTP53      p.Val272Met      p.Pro72Arg
      9n.a.TP53      p.Arg333Valfs*12
      10n.a.TP53      p.Pro72Arg
      11TP53      p.Cys275Trp      p.Pro72ArgTP53      p.Cys275Trp      p.Pro72Arg
      12n.a.TP53      p.Val216Met
      13TP53      p.Ile195Thr      p.Pro72ArgTP53      p.Ile195Thr      p.Pro72Arg
    Genetic variations in pCR patients
      1TP53p.Leu111Phefs*40
      2TP53p.Val157Phep.Pro72Arg
    Metp.Asn375Ser
      3TP53p.Cys141Tyrp.Pro72Arg
      4TP53p.Arg342*p.Pro72Arg
    FOXL2p.Leu130Gln
      5PIK3CAp.Arg1023Glnfs*4

    As a result, total of 3 somatic mutations in one gene (TP53) and six somatic mutations in two genes (TP53 and PTEN) were detected in biopsy samples (3/5 cases) and surgical specimens of PD/REC patients (6/8 cases), respectively. Somatic mutations were detected in three genes TP53, FOXL2 and PIK3CA in pCR patients (5/5 cases).

    TP53 was the most frequently mutated gene (9 of 13, 69.2% in total, 5 of 8, 62.5% in PD/REC cases and 4 of 5, 80% in pCR cases) (P = 0.50). Other pathogenic variants detected at a lower frequency were in genes PIK3CA (n = 1), PTEN (n = 1) and FOXL2 (n = 1). In both PD/REC and CR, unique pathogenic variants were detected in TP53 and other genes. As shown in the Table 3, the TP53 Pro72Arg polymorphism was detected in both pCR and PD/REC cases.

    Table 3

    Genotype of the TP53 Pro72Arg polymorphism

    Sample IDGenotypeAmino acidGenotypeRespose to chemothrapy
      1    C/C  Pro/Pro-                pCR
      2    C/G  Pro/ArgHeterozygote                pCR
      3    G/G  Arg/ArgHomozygote                pCR
      4    G/G  Arg/ArgHomozygote                pCR
      5    C/C  Pro/Pro-                pCR
      6    C/G  Pro/ArgHeterozygote                PD/REC
      7    C/G  Pro/ArgHeterozygote                PD/REC
      8    G/G  Arg/ArgHomozygote                PD/REC
      9    C/C  Pro/Pro-                PD/REC
      10    C/G  Pro/ArgHeterozygote                PD/REC
      11    G/G  Arg/ArgHomozygote                PD/REC
      12    C/C  Pro/Pro-                PD/REC
      13    C/C  Pro/Pro-                PD/REC

    Next, we compared the effect of chemotherapy in five matched cases showed PD/REC. In patient 7, the PTEN Ser179Valfs*8 mutation was detected after NAC, but it was seen before NAC at low frequency on one strand (2%). Other genetic variations (TP53 and STK11) were observed both pre- and post-treatment.

    Discussion

    In this study, we used NGS to analyze 26 genes of 13 TNBC tumors receiving NAC. This is the first report to determine genetic variations in Japanese TNBC patients who showed pCR and PD/REC as a result of NAC. TP53 pathogenic variants were detected in both pCR and PD/REC cases at frequencies similar to the high rates previously reported. TP53 genetic variations in pCR cases might be associated with sensitivity to chemotherapy, and other TP53 variants in PD/REC cases might affect resistance to chemotherapy. Thus, sensitivity to chemotherapy may vary by the location and type of somatic TP53 variants. However, we could not confirm whether these genetic alterations found in this study were responsible for the chemo-sensitivity and recurrence because the number of patients are too small.

    The numbers of genes and cases assessed were limited in this study. However, the frequency of genetic variations detected in TNBC did not differ greatly from those in previous studies. Lips et al.[10] analyzed 1977 genes in 56 pre-treatment TNBC biopsies of NAC responders and non-responders as well as matched normal DNA. They reported that most mutations were in TP53, TTN, and PIK3CA (55%, 14%, and 9%, respectively). No recurrent mutations were associated with chemotherapy response or relapse[10]. Balko et al.[11] examined residual disease in 74 clinically defined TNBCs after NAC, which included NGS performed on 20 matched pretreatment biopsies. Targeted NGS was carried out of 3320 exons from 182 oncogenes and tumor suppressors as well as 37 introns of 14 genes frequently rearranged in cancer. The frequency of each mutation was fewer than 5% of samples. Alterations in TP53 were identified in 72 of 81 samples (89%), which was a similar rate to that observed in other studies of basal-like breast cancer or TNBC, and The Cancer Genome Atlas dataset (~85%)[11]. Roy-Chowdhuri et al.[12] reported that a triple-negative group (n = 77) showed mutations in 15 of 46 genes tested, with TP53 showing the highest mutation frequency (n = 48/77, 62%), followed by PIK3CA (n = 13/77, 17%), APC, RET, SMAD4 (n = 2, 3%), AKT1, ATM, BRAF, FGFR1, HRAS, JAK3, MET, SRC, PTEN, and STK11 (n = 1, 1%)[12]. From these previous reports, it is difficult to conclude that the varied and sparse genetic alterations seen in the present study caused differences between responders and non-responders toward chemotherapy.

    TP53 mutations in breast cancer have previously been reported to be associated with worse prognosis[13,14]. Ooe et al.[15] investigated the relationship between the p53 mutation status and response to docetaxel in breast cancers. They found that the response rate of patients with p53-mutated tumors (44%) was lower than that of those with wild-type tumors (62%). In addition, the TP53 p.Pro72Arg polymorphism was reported association with platinum-based chemotherapy response in non-small cell lung cancer[16]. Platinum-based chemotherapy was only administered to one case in our study, so no response difference was detected between heterozygous and homozygous variants in the pCR or PD/REC group. However, the same genetic variations of TP53 (p.V157F and p.Cys141Tyr) detected in PD/REC samples in previous study[11] were also observed in pCR samples in our study.

    As a cohort, it is representative of Japanese TNBC, but the number of patients and samples was too low to confirm relevant relationship with genetic variants. This preliminary study should be followed up with a higher number of patients and selected genes in future.

    In this study, 8 of 13 TNBC tumors were found to have TP53 pathogenic variants, in both pCR and PD/REC cases. TP53 variations were detected at similarly high rates as previously reported and may be associated with sensitivity or resistance to chemotherapy depending on the location and type of the variant. If the effect of these genetic variations on the induction of apoptosis could be determined, this might enable the mechanism of the NAC chemotherapy response to be understood. Our results provide insights into potentially actionable variants for targeted therapeutic options in TNBC.

    Declarations

    Authors’ contributions

    Drafting of the manuscript, review and revisions of the final draft, data analysis and experiments: Mori M, Watanabe T, Makino R

    Experiments: Ueda K, Hirota Y

    Supervision, manuscript review and project administration: Akashi-Tanaka S, Nakamura S

    Availability of data and materials

    Not applicable.

    Financial support and sponsorship

    This work was supported in part by a Grant-in-Aid for the High-Technology Research Center Project from the Ministry of Education, Culture, Sports, Science and Technology of Japan.

    Conflicts of interest

    All authors declared that there are no conflicts of interest.

    Ethical approval and consent to participate

    This study was approved (number 1589) by the Institutional Review Board of Showa University, Japan. Written informed consent was received from the patients. If informed consent could not be received for the death of patients, the candidate opted out on the homepage of the hospital.

    Consent for publication

    Not applicable.

    Copyright

    © The Author(s) 2019.

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