TY - JOUR
T1 - Targeting Cytoprotective Autophagy to Enhance Anticancer Therapies
AU - Xiao, Malina
AU - Benoit, Alice
AU - Hasmim, Meriem
AU - Duhem, Caroline
AU - Vogin, Guillaume
AU - Berchem, Guy
AU - Noman, Muhammad Zaeem
AU - Janji, Bassam
N1 - Funding Information:
This work was supported by Luxembourg Institute of Health and grants from the Luxembourg National Research Fund (PRIDE15/10675146/CANBIO and C18/BM/12670304/ COMBATIC); FNRS Televie (grants 7.4606.18 and 7.4579.20); Fondation Cancer, Luxembourg (FC/2018/06); Kriibskrank Kanner Foundation, Luxembourg (2019); RCMS foundation, and Action LIONS Vaincre le Cancer Luxembourg. The authors also declare that this study received funding from Janssen Cilag Pharma and Roche Pharma. These funders were not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
Publisher Copyright:
© Copyright © 2021 Xiao, Benoit, Hasmim, Duhem, Vogin, Berchem, Noman and Janji.
PY - 2021/2/25
Y1 - 2021/2/25
N2 - 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.
AB - 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.
KW - autophagy
KW - cancer resistance
KW - chemotherapy
KW - immunotherapy
KW - radiotherapy
KW - targeted therapy
UR - http://www.scopus.com/inward/record.url?scp=85102437608&partnerID=8YFLogxK
UR - https://www.ncbi.nlm.nih.gov/pubmed/33718194
U2 - 10.3389/fonc.2021.626309
DO - 10.3389/fonc.2021.626309
M3 - Review article
C2 - 33718194
AN - SCOPUS:85102437608
SN - 2234-943X
VL - 11
SP - 626309
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 626309
ER -