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Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'

Glioblastoma multiforme is the most common and the most aggressive primary brain tumor. It is characterized by a high degree of hypoxia and also by a remarkable resistance to therapy because of its adaptation capabilities that include autophagy. This degradation process allows the recycling of cellu...

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Autores principales: Jawhari, Soha, Ratinaud, Marie-Hélène, Verdier, Mireille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133985/
https://www.ncbi.nlm.nih.gov/pubmed/27787518
http://dx.doi.org/10.1038/cddis.2016.318
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author Jawhari, Soha
Ratinaud, Marie-Hélène
Verdier, Mireille
author_facet Jawhari, Soha
Ratinaud, Marie-Hélène
Verdier, Mireille
author_sort Jawhari, Soha
collection PubMed
description Glioblastoma multiforme is the most common and the most aggressive primary brain tumor. It is characterized by a high degree of hypoxia and also by a remarkable resistance to therapy because of its adaptation capabilities that include autophagy. This degradation process allows the recycling of cellular components, leading to the formation of metabolic precursors and production of adenosine triphosphate. Hypoxia can induce autophagy through the activation of several autophagy-related proteins such as BNIP3, AMPK, REDD1, PML, and the unfolded protein response-related transcription factors ATF4 and CHOP. This review summarizes the most recent data about induction of autophagy under hypoxic condition and the role of autophagy in glioblastoma.
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spelling pubmed-51339852016-12-16 Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois' Jawhari, Soha Ratinaud, Marie-Hélène Verdier, Mireille Cell Death Dis Review Glioblastoma multiforme is the most common and the most aggressive primary brain tumor. It is characterized by a high degree of hypoxia and also by a remarkable resistance to therapy because of its adaptation capabilities that include autophagy. This degradation process allows the recycling of cellular components, leading to the formation of metabolic precursors and production of adenosine triphosphate. Hypoxia can induce autophagy through the activation of several autophagy-related proteins such as BNIP3, AMPK, REDD1, PML, and the unfolded protein response-related transcription factors ATF4 and CHOP. This review summarizes the most recent data about induction of autophagy under hypoxic condition and the role of autophagy in glioblastoma. Nature Publishing Group 2016-10 2016-10-27 /pmc/articles/PMC5133985/ /pubmed/27787518 http://dx.doi.org/10.1038/cddis.2016.318 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Review
Jawhari, Soha
Ratinaud, Marie-Hélène
Verdier, Mireille
Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'
title Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'
title_full Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'
title_fullStr Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'
title_full_unstemmed Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'
title_short Glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'
title_sort glioblastoma, hypoxia and autophagy: a survival-prone ‘ménage-à-trois'
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133985/
https://www.ncbi.nlm.nih.gov/pubmed/27787518
http://dx.doi.org/10.1038/cddis.2016.318
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