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GPER Function in Breast Cancer: An Overview

The G-protein-coupled estrogen receptor-1 (GPER, formerly known as GPR30) has attracted increasing interest, considering its ability to mediate estrogenic signaling in different cell types, including the hormone-sensitive tumors like breast cancer. As observed for other GPCR-mediated responses, the...

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Detalles Bibliográficos
Autores principales: Lappano, Rosamaria, Pisano, Assunta, Maggiolini, Marcello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018520/
https://www.ncbi.nlm.nih.gov/pubmed/24834064
http://dx.doi.org/10.3389/fendo.2014.00066
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author Lappano, Rosamaria
Pisano, Assunta
Maggiolini, Marcello
author_facet Lappano, Rosamaria
Pisano, Assunta
Maggiolini, Marcello
author_sort Lappano, Rosamaria
collection PubMed
description The G-protein-coupled estrogen receptor-1 (GPER, formerly known as GPR30) has attracted increasing interest, considering its ability to mediate estrogenic signaling in different cell types, including the hormone-sensitive tumors like breast cancer. As observed for other GPCR-mediated responses, the activation of the epidermal growth factor receptor is a fundamental integration point in the biological action triggered by GPER. A wide number of natural and synthetic compounds, including estrogens and anti-estrogens, elicit stimulatory effects in breast cancer through GPER up-regulation and activation, suggesting that GPER function is associated with breast tumor progression and tamoxifen resistance. GPER has also been proposed as a candidate biomarker in triple-negative breast cancer, opening a novel scenario for a more comprehensive assessment of breast tumor patients.
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spelling pubmed-40185202014-05-15 GPER Function in Breast Cancer: An Overview Lappano, Rosamaria Pisano, Assunta Maggiolini, Marcello Front Endocrinol (Lausanne) Endocrinology The G-protein-coupled estrogen receptor-1 (GPER, formerly known as GPR30) has attracted increasing interest, considering its ability to mediate estrogenic signaling in different cell types, including the hormone-sensitive tumors like breast cancer. As observed for other GPCR-mediated responses, the activation of the epidermal growth factor receptor is a fundamental integration point in the biological action triggered by GPER. A wide number of natural and synthetic compounds, including estrogens and anti-estrogens, elicit stimulatory effects in breast cancer through GPER up-regulation and activation, suggesting that GPER function is associated with breast tumor progression and tamoxifen resistance. GPER has also been proposed as a candidate biomarker in triple-negative breast cancer, opening a novel scenario for a more comprehensive assessment of breast tumor patients. Frontiers Media S.A. 2014-05-06 /pmc/articles/PMC4018520/ /pubmed/24834064 http://dx.doi.org/10.3389/fendo.2014.00066 Text en Copyright © 2014 Lappano, Pisano and Maggiolini. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Lappano, Rosamaria
Pisano, Assunta
Maggiolini, Marcello
GPER Function in Breast Cancer: An Overview
title GPER Function in Breast Cancer: An Overview
title_full GPER Function in Breast Cancer: An Overview
title_fullStr GPER Function in Breast Cancer: An Overview
title_full_unstemmed GPER Function in Breast Cancer: An Overview
title_short GPER Function in Breast Cancer: An Overview
title_sort gper function in breast cancer: an overview
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018520/
https://www.ncbi.nlm.nih.gov/pubmed/24834064
http://dx.doi.org/10.3389/fendo.2014.00066
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