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G-Protein Coupled Estrogen Receptor in Breast Cancer

The G-protein coupled estrogen receptor (GPER), an alternate estrogen receptor (ER) with a structure distinct from the two canonical ERs, being ERα, and ERβ, is expressed in 50% to 60% of breast cancer tissues and has been presumed to be associated with the development of tamoxifen resistance in ERα...

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Detalles Bibliográficos
Autores principales: Hsu, Li-Han, Chu, Nei-Min, Lin, Yung-Feng, Kao, Shu-Huei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359026/
https://www.ncbi.nlm.nih.gov/pubmed/30646517
http://dx.doi.org/10.3390/ijms20020306
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author Hsu, Li-Han
Chu, Nei-Min
Lin, Yung-Feng
Kao, Shu-Huei
author_facet Hsu, Li-Han
Chu, Nei-Min
Lin, Yung-Feng
Kao, Shu-Huei
author_sort Hsu, Li-Han
collection PubMed
description The G-protein coupled estrogen receptor (GPER), an alternate estrogen receptor (ER) with a structure distinct from the two canonical ERs, being ERα, and ERβ, is expressed in 50% to 60% of breast cancer tissues and has been presumed to be associated with the development of tamoxifen resistance in ERα positive breast cancer. On the other hand, triple-negative breast cancer (TNBC) constitutes 15% to 20% of breast cancers and frequently displays a more aggressive behavior. GPER is prevalent and involved in TNBC and can be a therapeutic target. However, contradictory results exist regarding the function of GPER in breast cancer, proliferative or pro-apoptotic. A better understanding of the GPER, its role in breast cancer, and the interactions with the ER and epidermal growth factor receptor will be beneficial for the disease management and prevention in the future.
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spelling pubmed-63590262019-02-06 G-Protein Coupled Estrogen Receptor in Breast Cancer Hsu, Li-Han Chu, Nei-Min Lin, Yung-Feng Kao, Shu-Huei Int J Mol Sci Review The G-protein coupled estrogen receptor (GPER), an alternate estrogen receptor (ER) with a structure distinct from the two canonical ERs, being ERα, and ERβ, is expressed in 50% to 60% of breast cancer tissues and has been presumed to be associated with the development of tamoxifen resistance in ERα positive breast cancer. On the other hand, triple-negative breast cancer (TNBC) constitutes 15% to 20% of breast cancers and frequently displays a more aggressive behavior. GPER is prevalent and involved in TNBC and can be a therapeutic target. However, contradictory results exist regarding the function of GPER in breast cancer, proliferative or pro-apoptotic. A better understanding of the GPER, its role in breast cancer, and the interactions with the ER and epidermal growth factor receptor will be beneficial for the disease management and prevention in the future. MDPI 2019-01-14 /pmc/articles/PMC6359026/ /pubmed/30646517 http://dx.doi.org/10.3390/ijms20020306 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hsu, Li-Han
Chu, Nei-Min
Lin, Yung-Feng
Kao, Shu-Huei
G-Protein Coupled Estrogen Receptor in Breast Cancer
title G-Protein Coupled Estrogen Receptor in Breast Cancer
title_full G-Protein Coupled Estrogen Receptor in Breast Cancer
title_fullStr G-Protein Coupled Estrogen Receptor in Breast Cancer
title_full_unstemmed G-Protein Coupled Estrogen Receptor in Breast Cancer
title_short G-Protein Coupled Estrogen Receptor in Breast Cancer
title_sort g-protein coupled estrogen receptor in breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359026/
https://www.ncbi.nlm.nih.gov/pubmed/30646517
http://dx.doi.org/10.3390/ijms20020306
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