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Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A

BACKGROUND: Hypoxia is negatively associated with glioblastoma (GBM) patient survival and contributes to tumour resistance. Anti-angiogenic therapy in GBM further increases hypoxia and activates survival pathways. The aim of this study was to determine the role of hypoxia-induced autophagy in GBM. M...

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Autores principales: Abdul Rahim, Siti Aminah, Dirkse, Anne, Oudin, Anais, Schuster, Anne, Bohler, Jill, Barthelemy, Vanessa, Muller, Arnaud, Vallar, Laurent, Janji, Bassam, Golebiewska, Anna, Niclou, Simone P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590001/
https://www.ncbi.nlm.nih.gov/pubmed/28797031
http://dx.doi.org/10.1038/bjc.2017.263
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author Abdul Rahim, Siti Aminah
Dirkse, Anne
Oudin, Anais
Schuster, Anne
Bohler, Jill
Barthelemy, Vanessa
Muller, Arnaud
Vallar, Laurent
Janji, Bassam
Golebiewska, Anna
Niclou, Simone P
author_facet Abdul Rahim, Siti Aminah
Dirkse, Anne
Oudin, Anais
Schuster, Anne
Bohler, Jill
Barthelemy, Vanessa
Muller, Arnaud
Vallar, Laurent
Janji, Bassam
Golebiewska, Anna
Niclou, Simone P
author_sort Abdul Rahim, Siti Aminah
collection PubMed
description BACKGROUND: Hypoxia is negatively associated with glioblastoma (GBM) patient survival and contributes to tumour resistance. Anti-angiogenic therapy in GBM further increases hypoxia and activates survival pathways. The aim of this study was to determine the role of hypoxia-induced autophagy in GBM. METHODS: Pharmacological inhibition of autophagy was applied in combination with bevacizumab in GBM patient-derived xenografts (PDXs). Sensitivity towards inhibitors was further tested in vitro under normoxia and hypoxia, followed by transcriptomic analysis. Genetic interference was done using ATG9A-depleted cells. RESULTS: We find that GBM cells activate autophagy as a survival mechanism to hypoxia, although basic autophagy appears active under normoxic conditions. Although single agent chloroquine treatment in vivo significantly increased survival of PDXs, the combination with bevacizumab resulted in a synergistic effect at low non-effective chloroquine dose. ATG9A was consistently induced by hypoxia, and silencing of ATG9A led to decreased proliferation in vitro and delayed tumour growth in vivo. Hypoxia-induced activation of autophagy was compromised upon ATG9A depletion. CONCLUSIONS: This work shows that inhibition of autophagy is a promising strategy against GBM and identifies ATG9 as a novel target in hypoxia-induced autophagy. Combination with hypoxia-inducing agents may provide benefit by allowing to decrease the effective dose of autophagy inhibitors.
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spelling pubmed-55900012018-09-05 Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A Abdul Rahim, Siti Aminah Dirkse, Anne Oudin, Anais Schuster, Anne Bohler, Jill Barthelemy, Vanessa Muller, Arnaud Vallar, Laurent Janji, Bassam Golebiewska, Anna Niclou, Simone P Br J Cancer Translational Therapeutics BACKGROUND: Hypoxia is negatively associated with glioblastoma (GBM) patient survival and contributes to tumour resistance. Anti-angiogenic therapy in GBM further increases hypoxia and activates survival pathways. The aim of this study was to determine the role of hypoxia-induced autophagy in GBM. METHODS: Pharmacological inhibition of autophagy was applied in combination with bevacizumab in GBM patient-derived xenografts (PDXs). Sensitivity towards inhibitors was further tested in vitro under normoxia and hypoxia, followed by transcriptomic analysis. Genetic interference was done using ATG9A-depleted cells. RESULTS: We find that GBM cells activate autophagy as a survival mechanism to hypoxia, although basic autophagy appears active under normoxic conditions. Although single agent chloroquine treatment in vivo significantly increased survival of PDXs, the combination with bevacizumab resulted in a synergistic effect at low non-effective chloroquine dose. ATG9A was consistently induced by hypoxia, and silencing of ATG9A led to decreased proliferation in vitro and delayed tumour growth in vivo. Hypoxia-induced activation of autophagy was compromised upon ATG9A depletion. CONCLUSIONS: This work shows that inhibition of autophagy is a promising strategy against GBM and identifies ATG9 as a novel target in hypoxia-induced autophagy. Combination with hypoxia-inducing agents may provide benefit by allowing to decrease the effective dose of autophagy inhibitors. Nature Publishing Group 2017-09-05 2017-08-10 /pmc/articles/PMC5590001/ /pubmed/28797031 http://dx.doi.org/10.1038/bjc.2017.263 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Translational Therapeutics
Abdul Rahim, Siti Aminah
Dirkse, Anne
Oudin, Anais
Schuster, Anne
Bohler, Jill
Barthelemy, Vanessa
Muller, Arnaud
Vallar, Laurent
Janji, Bassam
Golebiewska, Anna
Niclou, Simone P
Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A
title Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A
title_full Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A
title_fullStr Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A
title_full_unstemmed Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A
title_short Regulation of hypoxia-induced autophagy in glioblastoma involves ATG9A
title_sort regulation of hypoxia-induced autophagy in glioblastoma involves atg9a
topic Translational Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590001/
https://www.ncbi.nlm.nih.gov/pubmed/28797031
http://dx.doi.org/10.1038/bjc.2017.263
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