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Exosomes and their roles in the chemoresistance of pancreatic cancer

Pancreatic cancer (PC) remains one of the most lethal human malignancies worldwide. Due to the insidious onset and the rapid progression, most patients with PC are diagnosed at an advanced stage rendering them inoperable. Despite the development of multiple promising chemotherapeutic agents as recom...

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Detalles Bibliográficos
Autores principales: Pan, Yubin, Tang, Honglin, Li, Qijun, Chen, Guangpeng, Li, Da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761084/
https://www.ncbi.nlm.nih.gov/pubmed/35587712
http://dx.doi.org/10.1002/cam4.4830
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author Pan, Yubin
Tang, Honglin
Li, Qijun
Chen, Guangpeng
Li, Da
author_facet Pan, Yubin
Tang, Honglin
Li, Qijun
Chen, Guangpeng
Li, Da
author_sort Pan, Yubin
collection PubMed
description Pancreatic cancer (PC) remains one of the most lethal human malignancies worldwide. Due to the insidious onset and the rapid progression, most patients with PC are diagnosed at an advanced stage rendering them inoperable. Despite the development of multiple promising chemotherapeutic agents as recommended first‐line treatment for PC, the therapeutic efficacy is largely limited by unwanted drug resistance. Recent studies have identified exosomes as essential mediators of intercellular communications during the occurrence of drug resistance. Understanding the underlying molecular mechanisms and complex signaling pathways of exosome‐mediated drug resistance will contribute to the improvement of the design of new oncologic therapy regimens. This review focuses on the intrinsic connections between the chemoresistance of PC cells and exosomes in the tumor microenvironment (TME).
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spelling pubmed-97610842022-12-20 Exosomes and their roles in the chemoresistance of pancreatic cancer Pan, Yubin Tang, Honglin Li, Qijun Chen, Guangpeng Li, Da Cancer Med REVIEWS Pancreatic cancer (PC) remains one of the most lethal human malignancies worldwide. Due to the insidious onset and the rapid progression, most patients with PC are diagnosed at an advanced stage rendering them inoperable. Despite the development of multiple promising chemotherapeutic agents as recommended first‐line treatment for PC, the therapeutic efficacy is largely limited by unwanted drug resistance. Recent studies have identified exosomes as essential mediators of intercellular communications during the occurrence of drug resistance. Understanding the underlying molecular mechanisms and complex signaling pathways of exosome‐mediated drug resistance will contribute to the improvement of the design of new oncologic therapy regimens. This review focuses on the intrinsic connections between the chemoresistance of PC cells and exosomes in the tumor microenvironment (TME). John Wiley and Sons Inc. 2022-05-19 /pmc/articles/PMC9761084/ /pubmed/35587712 http://dx.doi.org/10.1002/cam4.4830 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle REVIEWS
Pan, Yubin
Tang, Honglin
Li, Qijun
Chen, Guangpeng
Li, Da
Exosomes and their roles in the chemoresistance of pancreatic cancer
title Exosomes and their roles in the chemoresistance of pancreatic cancer
title_full Exosomes and their roles in the chemoresistance of pancreatic cancer
title_fullStr Exosomes and their roles in the chemoresistance of pancreatic cancer
title_full_unstemmed Exosomes and their roles in the chemoresistance of pancreatic cancer
title_short Exosomes and their roles in the chemoresistance of pancreatic cancer
title_sort exosomes and their roles in the chemoresistance of pancreatic cancer
topic REVIEWS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761084/
https://www.ncbi.nlm.nih.gov/pubmed/35587712
http://dx.doi.org/10.1002/cam4.4830
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