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Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth
The estrogen receptor alpha (ERα) is highly expressed in both endometrial and breast cancers, and represents the most prevalent therapeutic target in breast cancer. However, anti-estrogen therapy has not been shown to be effective in endometrial cancer. Recently it has been shown that hormone-bindin...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861919/ https://www.ncbi.nlm.nih.gov/pubmed/27160768 http://dx.doi.org/10.1038/srep25521 |
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author | Holst, Frederik Hoivik, Erling A. Gibson, William J. Taylor-Weiner, Amaro Schumacher, Steven E. Asmann, Yan W. Grossmann, Patrick Trovik, Jone Necela, Brian M. Thompson, E. Aubrey Meyerson, Matthew Beroukhim, Rameen Salvesen, Helga B. Cherniack, Andrew D. |
author_facet | Holst, Frederik Hoivik, Erling A. Gibson, William J. Taylor-Weiner, Amaro Schumacher, Steven E. Asmann, Yan W. Grossmann, Patrick Trovik, Jone Necela, Brian M. Thompson, E. Aubrey Meyerson, Matthew Beroukhim, Rameen Salvesen, Helga B. Cherniack, Andrew D. |
author_sort | Holst, Frederik |
collection | PubMed |
description | The estrogen receptor alpha (ERα) is highly expressed in both endometrial and breast cancers, and represents the most prevalent therapeutic target in breast cancer. However, anti-estrogen therapy has not been shown to be effective in endometrial cancer. Recently it has been shown that hormone-binding domain alterations of ERα in breast cancer contribute to acquired resistance to anti-estrogen therapy. In analyses of genomic data from The Cancer Genome Atlas (TCGA), we observe that endometrial carcinomas manifest recurrent ESR1 gene amplifications that truncate the hormone-binding domain encoding region of ESR1 and are associated with reduced mRNA expression of exons encoding the hormone-binding domain. These findings support a role for hormone-binding alterations of ERα in primary endometrial cancer, with potentially important therapeutic implications. |
format | Online Article Text |
id | pubmed-4861919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48619192016-05-20 Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth Holst, Frederik Hoivik, Erling A. Gibson, William J. Taylor-Weiner, Amaro Schumacher, Steven E. Asmann, Yan W. Grossmann, Patrick Trovik, Jone Necela, Brian M. Thompson, E. Aubrey Meyerson, Matthew Beroukhim, Rameen Salvesen, Helga B. Cherniack, Andrew D. Sci Rep Article The estrogen receptor alpha (ERα) is highly expressed in both endometrial and breast cancers, and represents the most prevalent therapeutic target in breast cancer. However, anti-estrogen therapy has not been shown to be effective in endometrial cancer. Recently it has been shown that hormone-binding domain alterations of ERα in breast cancer contribute to acquired resistance to anti-estrogen therapy. In analyses of genomic data from The Cancer Genome Atlas (TCGA), we observe that endometrial carcinomas manifest recurrent ESR1 gene amplifications that truncate the hormone-binding domain encoding region of ESR1 and are associated with reduced mRNA expression of exons encoding the hormone-binding domain. These findings support a role for hormone-binding alterations of ERα in primary endometrial cancer, with potentially important therapeutic implications. Nature Publishing Group 2016-05-10 /pmc/articles/PMC4861919/ /pubmed/27160768 http://dx.doi.org/10.1038/srep25521 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Holst, Frederik Hoivik, Erling A. Gibson, William J. Taylor-Weiner, Amaro Schumacher, Steven E. Asmann, Yan W. Grossmann, Patrick Trovik, Jone Necela, Brian M. Thompson, E. Aubrey Meyerson, Matthew Beroukhim, Rameen Salvesen, Helga B. Cherniack, Andrew D. Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth |
title | Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth |
title_full | Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth |
title_fullStr | Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth |
title_full_unstemmed | Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth |
title_short | Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth |
title_sort | recurrent hormone-binding domain truncated esr1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861919/ https://www.ncbi.nlm.nih.gov/pubmed/27160768 http://dx.doi.org/10.1038/srep25521 |
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