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Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors

The G-protein-coupled estrogen receptor-1 (GPER-1), also known as GPR30, is a novel estrogen receptor mediating estrogen receptor signaling in multiple cell types. The progress of estrogen-related cancer is promoted by GPER-1 activation through mitogen-activated protein kinases (MAPK), phosphoinosit...

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Detalles Bibliográficos
Autores principales: Qian, Hongyan, Xuan, Jingxiu, Liu, Yuan, Shi, Guixiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4903118/
https://www.ncbi.nlm.nih.gov/pubmed/27314054
http://dx.doi.org/10.1155/2016/7128702
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author Qian, Hongyan
Xuan, Jingxiu
Liu, Yuan
Shi, Guixiu
author_facet Qian, Hongyan
Xuan, Jingxiu
Liu, Yuan
Shi, Guixiu
author_sort Qian, Hongyan
collection PubMed
description The G-protein-coupled estrogen receptor-1 (GPER-1), also known as GPR30, is a novel estrogen receptor mediating estrogen receptor signaling in multiple cell types. The progress of estrogen-related cancer is promoted by GPER-1 activation through mitogen-activated protein kinases (MAPK), phosphoinositide 3-kinase (PI3K), and phospholipase C (PLC) signaling pathways. However, this promoting effect of GPER-1 is nonclassic estrogen receptor (ER) dependent manner. In addition, clinical evidences revealed that GPER-1 is associated with estrogen resistance in estrogen-related cancer patients. These give a hint that GPER-1 may be a novel therapeutic target for the estrogen-related cancers. However, preclinical studies also found that GPER-1 activation of its special agonist G-1 inhibits cancer cell proliferation. This review aims to summarize the characteristics and complex functions of GPER-1 in cancers.
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spelling pubmed-49031182016-06-16 Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors Qian, Hongyan Xuan, Jingxiu Liu, Yuan Shi, Guixiu J Immunol Res Review Article The G-protein-coupled estrogen receptor-1 (GPER-1), also known as GPR30, is a novel estrogen receptor mediating estrogen receptor signaling in multiple cell types. The progress of estrogen-related cancer is promoted by GPER-1 activation through mitogen-activated protein kinases (MAPK), phosphoinositide 3-kinase (PI3K), and phospholipase C (PLC) signaling pathways. However, this promoting effect of GPER-1 is nonclassic estrogen receptor (ER) dependent manner. In addition, clinical evidences revealed that GPER-1 is associated with estrogen resistance in estrogen-related cancer patients. These give a hint that GPER-1 may be a novel therapeutic target for the estrogen-related cancers. However, preclinical studies also found that GPER-1 activation of its special agonist G-1 inhibits cancer cell proliferation. This review aims to summarize the characteristics and complex functions of GPER-1 in cancers. Hindawi Publishing Corporation 2016 2016-05-29 /pmc/articles/PMC4903118/ /pubmed/27314054 http://dx.doi.org/10.1155/2016/7128702 Text en Copyright © 2016 Hongyan Qian et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Qian, Hongyan
Xuan, Jingxiu
Liu, Yuan
Shi, Guixiu
Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors
title Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors
title_full Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors
title_fullStr Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors
title_full_unstemmed Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors
title_short Function of G-Protein-Coupled Estrogen Receptor-1 in Reproductive System Tumors
title_sort function of g-protein-coupled estrogen receptor-1 in reproductive system tumors
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4903118/
https://www.ncbi.nlm.nih.gov/pubmed/27314054
http://dx.doi.org/10.1155/2016/7128702
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