Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783262451710558208 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5590001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT abdulrahimsitiaminah regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT dirkseanne regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT oudinanais regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT schusteranne regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT bohlerjill regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT barthelemyvanessa regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT mullerarnaud regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT vallarlaurent regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT janjibassam regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT golebiewskaanna regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a AT niclousimonep regulationofhypoxiainducedautophagyinglioblastomainvolvesatg9a |