TY - JOUR
T1 - Extracellular Vesicles
T2 - New Classification and Tumor Immunosuppression
AU - Sheta, Mona
AU - Taha, Eman A.
AU - Lu, Yanyin
AU - Eguchi, Takanori
N1 - Funding Information:
M.S. was supported by Japan Society for the Promotion of Science (JSPS) International Research Fellowship in Japan. T.E. was supported by JSPS Kakenhi Grants 22F22409-TE, 22H03511-HO, 21H03119-TY, 21K08902-HY, 20H03888-HN, 20K20611-MT, 20K09904-CS, and 19H03817-MT, Wesco Scientific Promotion Foundation, and Okayama University.
Publisher Copyright:
© 2023 by the authors.
PY - 2023/1
Y1 - 2023/1
N2 - Extracellular vesicles (EVs) are cell-derived membrane-surrounded vesicles carrying various types of molecules. These EV cargoes are often used as pathophysiological biomarkers and delivered to recipient cells whose fates are often altered in local and distant tissues. Classical EVs are exosomes, microvesicles, and apoptotic bodies, while recent studies discovered autophagic EVs, stressed EVs, and matrix vesicles. Here, we classify classical and new EVs and non-EV nanoparticles. We also review EVs-mediated intercellular communication between cancer cells and various types of tumor-associated cells, such as cancer-associated fibroblasts, adipocytes, blood vessels, lymphatic vessels, and immune cells. Of note, cancer EVs play crucial roles in immunosuppression, immune evasion, and immunotherapy resistance. Thus, cancer EVs change hot tumors into cold ones. Moreover, cancer EVs affect nonimmune cells to promote cellular transformation, including epithelial-to-mesenchymal transition (EMT), chemoresistance, tumor matrix production, destruction of biological barriers, angiogenesis, lymphangiogenesis, and metastatic niche formation.
AB - Extracellular vesicles (EVs) are cell-derived membrane-surrounded vesicles carrying various types of molecules. These EV cargoes are often used as pathophysiological biomarkers and delivered to recipient cells whose fates are often altered in local and distant tissues. Classical EVs are exosomes, microvesicles, and apoptotic bodies, while recent studies discovered autophagic EVs, stressed EVs, and matrix vesicles. Here, we classify classical and new EVs and non-EV nanoparticles. We also review EVs-mediated intercellular communication between cancer cells and various types of tumor-associated cells, such as cancer-associated fibroblasts, adipocytes, blood vessels, lymphatic vessels, and immune cells. Of note, cancer EVs play crucial roles in immunosuppression, immune evasion, and immunotherapy resistance. Thus, cancer EVs change hot tumors into cold ones. Moreover, cancer EVs affect nonimmune cells to promote cellular transformation, including epithelial-to-mesenchymal transition (EMT), chemoresistance, tumor matrix production, destruction of biological barriers, angiogenesis, lymphangiogenesis, and metastatic niche formation.
KW - amphisome
KW - autophagy
KW - cellular communication
KW - exosome
KW - extracellular vesicle
KW - immune evasion
KW - immunosuppression
KW - matrix vesicle
KW - therapy resistance
KW - tumor microenvironment
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U2 - 10.3390/biology12010110
DO - 10.3390/biology12010110
M3 - Review article
AN - SCOPUS:85146746935
SN - 2079-7737
VL - 12
JO - Biology
JF - Biology
IS - 1
M1 - 110
ER -