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Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome

Api5 (Apoptosis inhibitor 5) is an anti-apoptotic factor that confers resistance to genotoxic stress in human cancer. Api5 is also expressed in endothelial cells and participates to the Estrogen Receptor α (ERα) signaling to promote cell migration. In this study, we found an over expression of Api5...

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Autores principales: Basset, Céline, Bonnet-Magnaval, Florence, Navarro, Marina Garcia-Jove, Touriol, Christian, Courtade, Monique, Prats, Hervé, Garmy-Susini, Barbara, Lacazette, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581047/
https://www.ncbi.nlm.nih.gov/pubmed/28881748
http://dx.doi.org/10.18632/oncotarget.17281
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author Basset, Céline
Bonnet-Magnaval, Florence
Navarro, Marina Garcia-Jove
Touriol, Christian
Courtade, Monique
Prats, Hervé
Garmy-Susini, Barbara
Lacazette, Eric
author_facet Basset, Céline
Bonnet-Magnaval, Florence
Navarro, Marina Garcia-Jove
Touriol, Christian
Courtade, Monique
Prats, Hervé
Garmy-Susini, Barbara
Lacazette, Eric
author_sort Basset, Céline
collection PubMed
description Api5 (Apoptosis inhibitor 5) is an anti-apoptotic factor that confers resistance to genotoxic stress in human cancer. Api5 is also expressed in endothelial cells and participates to the Estrogen Receptor α (ERα) signaling to promote cell migration. In this study, we found an over expression of Api5 in human breast cancer. Given that we show that high expression of Api5 in breast cancer patients is associated with shorter recurrence free survival, we investigated the relationship between ERα and Api5 at the molecular level. We found that Api5 Nuclear Receptor box (NR box) drives a direct interaction with the C domain of ERα. Furthermore, Api5 participates to gene transcription activation of ERα target genes upon estrogen treatment. Besides, Api5 expression favors tumorigenicity and migration and is necessary for tumor growth in vivo in mice xenografted model of breast cancer cell line. These finding suggest that Api5 is a new cofactor of ERα that functionally participates to the tumorigenic phenotype of breast cancer cells. In ERα breast cancer patients, Api5 overexpression is associated with poor survival, and may be used as a predictive marker of breast cancer recurrence free survival.
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spelling pubmed-55810472017-09-06 Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome Basset, Céline Bonnet-Magnaval, Florence Navarro, Marina Garcia-Jove Touriol, Christian Courtade, Monique Prats, Hervé Garmy-Susini, Barbara Lacazette, Eric Oncotarget Research Paper Api5 (Apoptosis inhibitor 5) is an anti-apoptotic factor that confers resistance to genotoxic stress in human cancer. Api5 is also expressed in endothelial cells and participates to the Estrogen Receptor α (ERα) signaling to promote cell migration. In this study, we found an over expression of Api5 in human breast cancer. Given that we show that high expression of Api5 in breast cancer patients is associated with shorter recurrence free survival, we investigated the relationship between ERα and Api5 at the molecular level. We found that Api5 Nuclear Receptor box (NR box) drives a direct interaction with the C domain of ERα. Furthermore, Api5 participates to gene transcription activation of ERα target genes upon estrogen treatment. Besides, Api5 expression favors tumorigenicity and migration and is necessary for tumor growth in vivo in mice xenografted model of breast cancer cell line. These finding suggest that Api5 is a new cofactor of ERα that functionally participates to the tumorigenic phenotype of breast cancer cells. In ERα breast cancer patients, Api5 overexpression is associated with poor survival, and may be used as a predictive marker of breast cancer recurrence free survival. Impact Journals LLC 2017-04-20 /pmc/articles/PMC5581047/ /pubmed/28881748 http://dx.doi.org/10.18632/oncotarget.17281 Text en Copyright: © 2017 Basset 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
Basset, Céline
Bonnet-Magnaval, Florence
Navarro, Marina Garcia-Jove
Touriol, Christian
Courtade, Monique
Prats, Hervé
Garmy-Susini, Barbara
Lacazette, Eric
Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome
title Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome
title_full Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome
title_fullStr Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome
title_full_unstemmed Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome
title_short Api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome
title_sort api5 a new cofactor of estrogen receptor alpha involved in breast cancer outcome
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581047/
https://www.ncbi.nlm.nih.gov/pubmed/28881748
http://dx.doi.org/10.18632/oncotarget.17281
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