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Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies

Autophagy is a highly regulated multi-step process that occurs at the basal level in almost all cells. Although the deregulation of the autophagy process has been described in several pathologies, the role of autophagy in cancer as a cytoprotective mechanism is currently well established and support...

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Autores principales: Xiao, Malina, Benoit, Alice, Hasmim, Meriem, Duhem, Caroline, Vogin, Guillaume, Berchem, Guy, Noman, Muhammad Zaeem, Janji, Bassam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951055/
https://www.ncbi.nlm.nih.gov/pubmed/33718194
http://dx.doi.org/10.3389/fonc.2021.626309
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author Xiao, Malina
Benoit, Alice
Hasmim, Meriem
Duhem, Caroline
Vogin, Guillaume
Berchem, Guy
Noman, Muhammad Zaeem
Janji, Bassam
author_facet Xiao, Malina
Benoit, Alice
Hasmim, Meriem
Duhem, Caroline
Vogin, Guillaume
Berchem, Guy
Noman, Muhammad Zaeem
Janji, Bassam
author_sort Xiao, Malina
collection PubMed
description Autophagy is a highly regulated multi-step process that occurs at the basal level in almost all cells. Although the deregulation of the autophagy process has been described in several pathologies, the role of autophagy in cancer as a cytoprotective mechanism is currently well established and supported by experimental and clinical evidence. Our understanding of the molecular mechanism of the autophagy process has largely contributed to defining how we can harness this process to improve the benefit of cancer therapies. While the role of autophagy in tumor resistance to chemotherapy is extensively documented, emerging data point toward autophagy as a mechanism of cancer resistance to radiotherapy, targeted therapy, and immunotherapy. Therefore, manipulating autophagy has emerged as a promising strategy to overcome tumor resistance to various anti-cancer therapies, and autophagy modulators are currently evaluated in combination therapies in several clinical trials. In this review, we will summarize our current knowledge of the impact of genetically and pharmacologically modulating autophagy genes and proteins, involved in the different steps of the autophagy process, on the therapeutic benefit of various cancer therapies. We will also briefly discuss the challenges and limitations to developing potent and selective autophagy inhibitors that could be used in ongoing clinical trials.
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spelling pubmed-79510552021-03-12 Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies Xiao, Malina Benoit, Alice Hasmim, Meriem Duhem, Caroline Vogin, Guillaume Berchem, Guy Noman, Muhammad Zaeem Janji, Bassam Front Oncol Oncology Autophagy is a highly regulated multi-step process that occurs at the basal level in almost all cells. Although the deregulation of the autophagy process has been described in several pathologies, the role of autophagy in cancer as a cytoprotective mechanism is currently well established and supported by experimental and clinical evidence. Our understanding of the molecular mechanism of the autophagy process has largely contributed to defining how we can harness this process to improve the benefit of cancer therapies. While the role of autophagy in tumor resistance to chemotherapy is extensively documented, emerging data point toward autophagy as a mechanism of cancer resistance to radiotherapy, targeted therapy, and immunotherapy. Therefore, manipulating autophagy has emerged as a promising strategy to overcome tumor resistance to various anti-cancer therapies, and autophagy modulators are currently evaluated in combination therapies in several clinical trials. In this review, we will summarize our current knowledge of the impact of genetically and pharmacologically modulating autophagy genes and proteins, involved in the different steps of the autophagy process, on the therapeutic benefit of various cancer therapies. We will also briefly discuss the challenges and limitations to developing potent and selective autophagy inhibitors that could be used in ongoing clinical trials. Frontiers Media S.A. 2021-02-25 /pmc/articles/PMC7951055/ /pubmed/33718194 http://dx.doi.org/10.3389/fonc.2021.626309 Text en Copyright © 2021 Xiao, Benoit, Hasmim, Duhem, Vogin, Berchem, Noman and Janji http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Xiao, Malina
Benoit, Alice
Hasmim, Meriem
Duhem, Caroline
Vogin, Guillaume
Berchem, Guy
Noman, Muhammad Zaeem
Janji, Bassam
Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies
title Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies
title_full Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies
title_fullStr Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies
title_full_unstemmed Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies
title_short Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies
title_sort targeting cytoprotective autophagy to enhance anticancer therapies
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951055/
https://www.ncbi.nlm.nih.gov/pubmed/33718194
http://dx.doi.org/10.3389/fonc.2021.626309
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