fig1

Tumor-derived exosomes: immune properties and clinical application in lung cancer

Figure 1. Molecular composition, biogenesis, release, and uptake of tumor-derived exosomes (TEXs). (A) TEXs originate from intraluminal vesicles (ILVs) in the multivesicular bodies (MVBs) (also known as late endosomes). Firstly, early endosomes (EEs) are formed when the membrane microdomains are endocytosed via inward budding of the plasma membrane. Then EEs mature into MVBs, which follow either fusion with the plasma membrane to form exosomes or degradation by lysosome. During this process, the proteins, nucleic acids, and lipids are packed into exosomes. Finally, exosomes can interact with recipient cells through three main ways: endocytosis/phagocytosis, direct fusion with cellular membrane, and receptor-ligand interactions. (B) Schematic diagram of components of TEXs.

Cancer Drug Resistance
ISSN 2578-532X (Online)

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