Cargando…

Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer

Mounting evidence indicates that tumor-derived exosomes (TDEs) play critical roles in tumor development and progression by regulating components in the tumor microenvironment (TME) in an autocrine or paracrine manner. Moreover, due to their delivery of critical molecules that react to chemotherapy a...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Ye, Chen, Zhuo-Kun, Duan, Xu, Zhang, He-Jing, Xiao, Bo-Lin, Wang, Kui-Ming, Chen, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534887/
https://www.ncbi.nlm.nih.gov/pubmed/36117219
http://dx.doi.org/10.1038/s12276-022-00856-3
_version_ 1784802647809720320
author Li, Ye
Chen, Zhuo-Kun
Duan, Xu
Zhang, He-Jing
Xiao, Bo-Lin
Wang, Kui-Ming
Chen, Gang
author_facet Li, Ye
Chen, Zhuo-Kun
Duan, Xu
Zhang, He-Jing
Xiao, Bo-Lin
Wang, Kui-Ming
Chen, Gang
author_sort Li, Ye
collection PubMed
description Mounting evidence indicates that tumor-derived exosomes (TDEs) play critical roles in tumor development and progression by regulating components in the tumor microenvironment (TME) in an autocrine or paracrine manner. Moreover, due to their delivery of critical molecules that react to chemotherapy and immunotherapy, TDEs also contribute to tumor drug resistance and impede the effective response of antitumor immunotherapy, thereby leading to poor clinical outcomes. There is a pressing need for the inhibition or removal of TDEs to facilitate the treatment and prognosis of cancer patients. Here, in the present review, we systematically overviewed the current strategies for TDE inhibition and clearance, providing novel insights for future tumor interventions in translational medicine. Moreover, existing challenges and potential prospects for TDE-targeted cancer therapy are also discussed to bridge the gaps between progress and promising applications.
format Online
Article
Text
id pubmed-9534887
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-95348872022-10-20 Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer Li, Ye Chen, Zhuo-Kun Duan, Xu Zhang, He-Jing Xiao, Bo-Lin Wang, Kui-Ming Chen, Gang Exp Mol Med Review Article Mounting evidence indicates that tumor-derived exosomes (TDEs) play critical roles in tumor development and progression by regulating components in the tumor microenvironment (TME) in an autocrine or paracrine manner. Moreover, due to their delivery of critical molecules that react to chemotherapy and immunotherapy, TDEs also contribute to tumor drug resistance and impede the effective response of antitumor immunotherapy, thereby leading to poor clinical outcomes. There is a pressing need for the inhibition or removal of TDEs to facilitate the treatment and prognosis of cancer patients. Here, in the present review, we systematically overviewed the current strategies for TDE inhibition and clearance, providing novel insights for future tumor interventions in translational medicine. Moreover, existing challenges and potential prospects for TDE-targeted cancer therapy are also discussed to bridge the gaps between progress and promising applications. Nature Publishing Group UK 2022-09-18 /pmc/articles/PMC9534887/ /pubmed/36117219 http://dx.doi.org/10.1038/s12276-022-00856-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Li, Ye
Chen, Zhuo-Kun
Duan, Xu
Zhang, He-Jing
Xiao, Bo-Lin
Wang, Kui-Ming
Chen, Gang
Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer
title Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer
title_full Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer
title_fullStr Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer
title_full_unstemmed Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer
title_short Targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer
title_sort targeted inhibition of tumor-derived exosomes as a novel therapeutic option for cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534887/
https://www.ncbi.nlm.nih.gov/pubmed/36117219
http://dx.doi.org/10.1038/s12276-022-00856-3
work_keys_str_mv AT liye targetedinhibitionoftumorderivedexosomesasanoveltherapeuticoptionforcancer
AT chenzhuokun targetedinhibitionoftumorderivedexosomesasanoveltherapeuticoptionforcancer
AT duanxu targetedinhibitionoftumorderivedexosomesasanoveltherapeuticoptionforcancer
AT zhanghejing targetedinhibitionoftumorderivedexosomesasanoveltherapeuticoptionforcancer
AT xiaobolin targetedinhibitionoftumorderivedexosomesasanoveltherapeuticoptionforcancer
AT wangkuiming targetedinhibitionoftumorderivedexosomesasanoveltherapeuticoptionforcancer
AT chengang targetedinhibitionoftumorderivedexosomesasanoveltherapeuticoptionforcancer