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AMBRA1 and its role as a target for anticancer therapy

The activating molecule in Beclin1-regulated autophagy protein 1 (AMBRA1) is an intrinsically disordered protein that regulates the survival and death of cancer cells by modulating autophagy. Although the roles of autophagy in cancer are controversial and context-dependent, inhibition of autophagy u...

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Autores principales: Li, Xiang, Lyu, Yuan, Li, Junqi, Wang, Xinjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551033/
https://www.ncbi.nlm.nih.gov/pubmed/36237336
http://dx.doi.org/10.3389/fonc.2022.946086
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author Li, Xiang
Lyu, Yuan
Li, Junqi
Wang, Xinjun
author_facet Li, Xiang
Lyu, Yuan
Li, Junqi
Wang, Xinjun
author_sort Li, Xiang
collection PubMed
description The activating molecule in Beclin1-regulated autophagy protein 1 (AMBRA1) is an intrinsically disordered protein that regulates the survival and death of cancer cells by modulating autophagy. Although the roles of autophagy in cancer are controversial and context-dependent, inhibition of autophagy under some circumstances can be a useful strategy for cancer therapy. As AMBRA1 is a pivotal autophagy-associated protein, targeting AMBRA1 similarly may be an underlying strategy for cancer therapy. Emerging evidence indicates that AMBRA1 can also inhibit cancer formation, maintenance, and progression by regulating c-MYC and cyclins, which are frequently deregulated in human cancer cells. Therefore, AMBRA1 is at the crossroad of autophagy, tumorigenesis, proliferation, and cell cycle. In this review, we focus on discussing the mechanisms of AMBRA1 in autophagy, mitophagy, and apoptosis, and particularly the roles of AMBRA1 in tumorigenesis and targeted therapy.
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spelling pubmed-95510332022-10-12 AMBRA1 and its role as a target for anticancer therapy Li, Xiang Lyu, Yuan Li, Junqi Wang, Xinjun Front Oncol Oncology The activating molecule in Beclin1-regulated autophagy protein 1 (AMBRA1) is an intrinsically disordered protein that regulates the survival and death of cancer cells by modulating autophagy. Although the roles of autophagy in cancer are controversial and context-dependent, inhibition of autophagy under some circumstances can be a useful strategy for cancer therapy. As AMBRA1 is a pivotal autophagy-associated protein, targeting AMBRA1 similarly may be an underlying strategy for cancer therapy. Emerging evidence indicates that AMBRA1 can also inhibit cancer formation, maintenance, and progression by regulating c-MYC and cyclins, which are frequently deregulated in human cancer cells. Therefore, AMBRA1 is at the crossroad of autophagy, tumorigenesis, proliferation, and cell cycle. In this review, we focus on discussing the mechanisms of AMBRA1 in autophagy, mitophagy, and apoptosis, and particularly the roles of AMBRA1 in tumorigenesis and targeted therapy. Frontiers Media S.A. 2022-09-27 /pmc/articles/PMC9551033/ /pubmed/36237336 http://dx.doi.org/10.3389/fonc.2022.946086 Text en Copyright © 2022 Li, Lyu, Li and Wang https://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
Li, Xiang
Lyu, Yuan
Li, Junqi
Wang, Xinjun
AMBRA1 and its role as a target for anticancer therapy
title AMBRA1 and its role as a target for anticancer therapy
title_full AMBRA1 and its role as a target for anticancer therapy
title_fullStr AMBRA1 and its role as a target for anticancer therapy
title_full_unstemmed AMBRA1 and its role as a target for anticancer therapy
title_short AMBRA1 and its role as a target for anticancer therapy
title_sort ambra1 and its role as a target for anticancer therapy
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551033/
https://www.ncbi.nlm.nih.gov/pubmed/36237336
http://dx.doi.org/10.3389/fonc.2022.946086
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