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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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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. |
format | Online Article Text |
id | pubmed-5581047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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