G protein-coupled estrogen receptor biased signaling in health and disease

IF 12.5 1区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmacology & Therapeutics Pub Date : 2025-05-01 Epub Date: 2025-02-18 DOI:10.1016/j.pharmthera.2025.108822
Aisha Bushi , Yixuan Ma , Joseph Adu-Amankwaah , Rong Wang , Fen Cui , Rui Xiao , Jinming Zhao , Jinxiang Yuan , Rubin Tan
{"title":"G protein-coupled estrogen receptor biased signaling in health and disease","authors":"Aisha Bushi ,&nbsp;Yixuan Ma ,&nbsp;Joseph Adu-Amankwaah ,&nbsp;Rong Wang ,&nbsp;Fen Cui ,&nbsp;Rui Xiao ,&nbsp;Jinming Zhao ,&nbsp;Jinxiang Yuan ,&nbsp;Rubin Tan","doi":"10.1016/j.pharmthera.2025.108822","DOIUrl":null,"url":null,"abstract":"<div><div>G protein-coupled estrogen receptor (GPER) is now recognized for its pivotal role in cellular signaling, influencing diverse physiological processes and disease states. Unlike classical estrogen receptors, GPER exhibits biased signaling, wherein ligand binding triggers selective pathways over others, significantly impacting cellular responses. This review explores the nuanced mechanisms of biased signaling mediated by GPER, underscoring its relevance in cardiovascular health, neurological function, immune modulation, and oncogenic processes. Despite its critical implications, biased signaling through GPER remains underexplored compared to traditional signaling paradigms. We explore recent progress in understanding GPER signaling specificity and its potential therapeutic implications across various diseases. Future research directions aim to uncover the molecular basis of biased signaling, develop selective ligands, and translate these insights into personalized therapeutic approaches. Exploiting the therapeutic potential of GPER biased signaling represents a promising frontier in precision medicine, offering innovative strategies to address unmet medical needs.</div></div>","PeriodicalId":402,"journal":{"name":"Pharmacology & Therapeutics","volume":"269 ","pages":"Article 108822"},"PeriodicalIF":12.5000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology & Therapeutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0163725825000348","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/18 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

G protein-coupled estrogen receptor (GPER) is now recognized for its pivotal role in cellular signaling, influencing diverse physiological processes and disease states. Unlike classical estrogen receptors, GPER exhibits biased signaling, wherein ligand binding triggers selective pathways over others, significantly impacting cellular responses. This review explores the nuanced mechanisms of biased signaling mediated by GPER, underscoring its relevance in cardiovascular health, neurological function, immune modulation, and oncogenic processes. Despite its critical implications, biased signaling through GPER remains underexplored compared to traditional signaling paradigms. We explore recent progress in understanding GPER signaling specificity and its potential therapeutic implications across various diseases. Future research directions aim to uncover the molecular basis of biased signaling, develop selective ligands, and translate these insights into personalized therapeutic approaches. Exploiting the therapeutic potential of GPER biased signaling represents a promising frontier in precision medicine, offering innovative strategies to address unmet medical needs.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
G蛋白偶联雌激素受体偏倚信号在健康和疾病中的作用。
G蛋白偶联雌激素受体(GPER)在细胞信号传导中起着关键作用,影响多种生理过程和疾病状态。与经典雌激素受体不同,GPER表现出偏置信号,其中配体结合触发选择性途径,显著影响细胞反应。这篇综述探讨了GPER介导的偏倚信号的细微机制,强调了其在心血管健康、神经功能、免疫调节和致癌过程中的相关性。尽管其具有重要意义,但与传统的信号范式相比,通过GPER进行的偏置信号仍未得到充分探索。我们探讨了了解GPER信号特异性及其在各种疾病中的潜在治疗意义的最新进展。未来的研究方向旨在揭示偏倚信号的分子基础,开发选择性配体,并将这些见解转化为个性化的治疗方法。利用GPER偏倚信号的治疗潜力代表了精准医学的一个有前途的前沿,为解决未满足的医疗需求提供了创新的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
23.00
自引率
0.70%
发文量
222
审稿时长
90 days
期刊介绍: Pharmacology & Therapeutics, in its 20th year, delivers lucid, critical, and authoritative reviews on current pharmacological topics.Articles, commissioned by the editor, follow specific author instructions.This journal maintains its scientific excellence and ranks among the top 10 most cited journals in pharmacology.
期刊最新文献
P2Y14 receptor in the nervous system: Pharmacology, mechanisms, and therapeutic potential Antiarrhythmic drugs to prevent sudden cardiac death: Is there a way forward? Insights into effective protocol structuring: optimizing dosing strategies, experimental design, and statistical approaches NETosis in ischemic stroke: Mechanisms, implications, and therapeutic prospects Wnt signaling pathway: Therapeutic target of natural products for cancer therapy
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1