G Protein-Coupled Estrogen Receptor GPER: Molecular Pharmacology and Therapeutic Applications

被引:58
作者
Arterburn, Jeffrey B. [1 ]
Prossnitz, Eric R. [2 ,3 ,4 ]
机构
[1] New Mexico State Univ, Dept Chem & Biochem, Las Cruces, NM USA
[2] Univ New Mexico, Hlth Sci Ctr, Ctr Comprehens Canc, Albuquerque, NM 87131 USA
[3] Univ New Mexico, Hlth Sci Ctr, Ctr Biomed Res Excellence Autophagy Inflammat & M, Albuquerque, NM 87131 USA
[4] Univ New Mexico, Hlth Sci Ctr, Dept Internal Med, Div Mol Med, Albuquerque, NM 87131 USA
基金
美国国家卫生研究院;
关键词
cancer; cardiovascular; endocrine; estrogen; immunity; metabolism; BREAST-CANCER CELLS; GROWTH-FACTOR RECEPTOR; GLOBAL CEREBRAL-ISCHEMIA; GENE-EXPRESSION CHANGES; AGONIST G-1; 30; GPR30; NITRIC-OXIDE; INTERNATIONAL-UNION; METABOLIC SYNDROME; PROTECTIVE ROLE;
D O I
10.1146/annurev-pharmtox-031122-121944
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The actions of estrogens and related estrogenic molecules are complex and multifaceted in both sexes. A wide array of natural, synthetic, and therapeutic molecules target pathways that produce and respond to estrogens. Multiple receptors promulgate these responses, including the classical estrogen receptors of the nuclear hormone receptor family (estrogen receptors a and beta), which function largely as ligand-activated transcription factors, and the 7-transmembrane G protein-coupled estrogen receptor, GPER, which activates a diverse array of signaling pathways. The pharmacology and functional roles of GPER in physiology and disease reveal important roles in responses to both natural and synthetic estrogenic compounds in numerous physiological systems. These functions have implications in the treatment of myriad disease states, including cancer, cardiovascular diseases, and metabolic disorders. This review focuses on the complex pharmacology of GPER and summarizes major physiological functions of GPER and the therapeutic implications and ongoing applications of GPER-targeted compounds.
引用
收藏
页码:295 / 320
页数:26
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