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GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells

The GABARAPL1 protein belongs to the ATG8 family whose members are involved in autophagy. Our laboratory previously demonstrated that GABARAPL1 associates with autophagic vesicles, regulates autophagic flux and acts as a tumor suppressor protein in breast cancer. In this study, we aimed to determine...

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Autores principales: Poillet-Perez, Laura, Jacquet, Marine, Hervouet, Eric, Gauthier, Thierry, Fraichard, Annick, Borg, Christophe, Pallandre, Jean-René, Gonzalez, Bruno J., Ramdani, Yasmina, Boyer-Guittaut, Michaël, Delage-Mourroux, Régis, Despouy, Gilles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593540/
https://www.ncbi.nlm.nih.gov/pubmed/28915569
http://dx.doi.org/10.18632/oncotarget.19639
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author Poillet-Perez, Laura
Jacquet, Marine
Hervouet, Eric
Gauthier, Thierry
Fraichard, Annick
Borg, Christophe
Pallandre, Jean-René
Gonzalez, Bruno J.
Ramdani, Yasmina
Boyer-Guittaut, Michaël
Delage-Mourroux, Régis
Despouy, Gilles
author_facet Poillet-Perez, Laura
Jacquet, Marine
Hervouet, Eric
Gauthier, Thierry
Fraichard, Annick
Borg, Christophe
Pallandre, Jean-René
Gonzalez, Bruno J.
Ramdani, Yasmina
Boyer-Guittaut, Michaël
Delage-Mourroux, Régis
Despouy, Gilles
author_sort Poillet-Perez, Laura
collection PubMed
description The GABARAPL1 protein belongs to the ATG8 family whose members are involved in autophagy. Our laboratory previously demonstrated that GABARAPL1 associates with autophagic vesicles, regulates autophagic flux and acts as a tumor suppressor protein in breast cancer. In this study, we aimed to determine whether GABARAPL1 conjugation to autophagosomes is necessary for its tumor suppressive functions using the MCF-7 breast cancer cell line overexpressing GABARAPL1 or a G116A mutant, which is unable to be lipidated and associated to autophagosomes. We show that the G116A mutation impaired GABARAPL1 function in autophagosome/lysosome fusion and inhibited lysosome activity but did not alter MTOR and ULK1 activities or tumor growth in vivo. Our results demonstrate for the first time that GABARAPL1 plays different regulatory functions during early and late stages of autophagy, independently or not of its conjugation to autophagosomes, but its tumor suppressive function appeared to be independent of its conjugation to autophagic vesicles.
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spelling pubmed-55935402017-09-14 GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells Poillet-Perez, Laura Jacquet, Marine Hervouet, Eric Gauthier, Thierry Fraichard, Annick Borg, Christophe Pallandre, Jean-René Gonzalez, Bruno J. Ramdani, Yasmina Boyer-Guittaut, Michaël Delage-Mourroux, Régis Despouy, Gilles Oncotarget Research Paper: Autophagy and Cell Death The GABARAPL1 protein belongs to the ATG8 family whose members are involved in autophagy. Our laboratory previously demonstrated that GABARAPL1 associates with autophagic vesicles, regulates autophagic flux and acts as a tumor suppressor protein in breast cancer. In this study, we aimed to determine whether GABARAPL1 conjugation to autophagosomes is necessary for its tumor suppressive functions using the MCF-7 breast cancer cell line overexpressing GABARAPL1 or a G116A mutant, which is unable to be lipidated and associated to autophagosomes. We show that the G116A mutation impaired GABARAPL1 function in autophagosome/lysosome fusion and inhibited lysosome activity but did not alter MTOR and ULK1 activities or tumor growth in vivo. Our results demonstrate for the first time that GABARAPL1 plays different regulatory functions during early and late stages of autophagy, independently or not of its conjugation to autophagosomes, but its tumor suppressive function appeared to be independent of its conjugation to autophagic vesicles. Impact Journals LLC 2017-07-27 /pmc/articles/PMC5593540/ /pubmed/28915569 http://dx.doi.org/10.18632/oncotarget.19639 Text en Copyright: © 2017 Poillet-Perez et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper: Autophagy and Cell Death
Poillet-Perez, Laura
Jacquet, Marine
Hervouet, Eric
Gauthier, Thierry
Fraichard, Annick
Borg, Christophe
Pallandre, Jean-René
Gonzalez, Bruno J.
Ramdani, Yasmina
Boyer-Guittaut, Michaël
Delage-Mourroux, Régis
Despouy, Gilles
GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells
title GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells
title_full GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells
title_fullStr GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells
title_full_unstemmed GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells
title_short GABARAPL1 tumor suppressive function is independent of its conjugation to autophagosomes in MCF-7 breast cancer cells
title_sort gabarapl1 tumor suppressive function is independent of its conjugation to autophagosomes in mcf-7 breast cancer cells
topic Research Paper: Autophagy and Cell Death
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593540/
https://www.ncbi.nlm.nih.gov/pubmed/28915569
http://dx.doi.org/10.18632/oncotarget.19639
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