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The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity
During tumorigenesis, cancer cells are exposed to a wide variety of intrinsic and extrinsic stresses that challenge homeostasis and growth. Cancer cells display activation of distinct mechanisms for adaptation and growth even in the presence of stress. Autophagy is a catabolic mechanism that aides i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575731/ https://www.ncbi.nlm.nih.gov/pubmed/33117715 http://dx.doi.org/10.3389/fonc.2020.578418 |
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author | Chavez-Dominguez, Rodolfo Perez-Medina, Mario Lopez-Gonzalez, Jose S. Galicia-Velasco, Miriam Aguilar-Cazares, Dolores |
author_facet | Chavez-Dominguez, Rodolfo Perez-Medina, Mario Lopez-Gonzalez, Jose S. Galicia-Velasco, Miriam Aguilar-Cazares, Dolores |
author_sort | Chavez-Dominguez, Rodolfo |
collection | PubMed |
description | During tumorigenesis, cancer cells are exposed to a wide variety of intrinsic and extrinsic stresses that challenge homeostasis and growth. Cancer cells display activation of distinct mechanisms for adaptation and growth even in the presence of stress. Autophagy is a catabolic mechanism that aides in the degradation of damaged intracellular material and metabolite recycling. This activity helps meet metabolic needs during nutrient deprivation, genotoxic stress, growth factor withdrawal and hypoxia. However, autophagy plays a paradoxical role in tumorigenesis, depending on the stage of tumor development. Early in tumorigenesis, autophagy is a tumor suppressor via degradation of potentially oncogenic molecules. However, in advanced stages, autophagy promotes the survival of tumor cells by ameliorating stress in the microenvironment. These roles of autophagy are intricate due to their interconnection with other distinct cellular pathways. In this review, we present a broad view of the participation of autophagy in distinct phases of tumor development. Moreover, autophagy participation in important cellular processes such as cell death, metabolic reprogramming, metastasis, immune evasion and treatment resistance that all contribute to tumor development, is reviewed. Finally, the contribution of the hypoxic and nutrient deficient tumor microenvironment in regulation of autophagy and these hallmarks for the development of more aggressive tumors is discussed. |
format | Online Article Text |
id | pubmed-7575731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75757312020-10-27 The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity Chavez-Dominguez, Rodolfo Perez-Medina, Mario Lopez-Gonzalez, Jose S. Galicia-Velasco, Miriam Aguilar-Cazares, Dolores Front Oncol Oncology During tumorigenesis, cancer cells are exposed to a wide variety of intrinsic and extrinsic stresses that challenge homeostasis and growth. Cancer cells display activation of distinct mechanisms for adaptation and growth even in the presence of stress. Autophagy is a catabolic mechanism that aides in the degradation of damaged intracellular material and metabolite recycling. This activity helps meet metabolic needs during nutrient deprivation, genotoxic stress, growth factor withdrawal and hypoxia. However, autophagy plays a paradoxical role in tumorigenesis, depending on the stage of tumor development. Early in tumorigenesis, autophagy is a tumor suppressor via degradation of potentially oncogenic molecules. However, in advanced stages, autophagy promotes the survival of tumor cells by ameliorating stress in the microenvironment. These roles of autophagy are intricate due to their interconnection with other distinct cellular pathways. In this review, we present a broad view of the participation of autophagy in distinct phases of tumor development. Moreover, autophagy participation in important cellular processes such as cell death, metabolic reprogramming, metastasis, immune evasion and treatment resistance that all contribute to tumor development, is reviewed. Finally, the contribution of the hypoxic and nutrient deficient tumor microenvironment in regulation of autophagy and these hallmarks for the development of more aggressive tumors is discussed. Frontiers Media S.A. 2020-10-07 /pmc/articles/PMC7575731/ /pubmed/33117715 http://dx.doi.org/10.3389/fonc.2020.578418 Text en Copyright © 2020 Chavez-Dominguez, Perez-Medina, Lopez-Gonzalez, Galicia-Velasco and Aguilar-Cazares. 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 Chavez-Dominguez, Rodolfo Perez-Medina, Mario Lopez-Gonzalez, Jose S. Galicia-Velasco, Miriam Aguilar-Cazares, Dolores The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity |
title | The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity |
title_full | The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity |
title_fullStr | The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity |
title_full_unstemmed | The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity |
title_short | The Double-Edge Sword of Autophagy in Cancer: From Tumor Suppression to Pro-tumor Activity |
title_sort | double-edge sword of autophagy in cancer: from tumor suppression to pro-tumor activity |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575731/ https://www.ncbi.nlm.nih.gov/pubmed/33117715 http://dx.doi.org/10.3389/fonc.2020.578418 |
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