Research Progress in Estrogen-related Receptor Gamma (ERRγ) Agonists and Inverse Agonists

被引:3
|
作者
Zheng, Yong [1 ]
Du, Yongli [1 ]
Zhang, Haibin [1 ]
Lv, Huiting [1 ]
Yan, Zhijia [1 ]
Dong, Ning [1 ]
Li, Qunyi [2 ]
Wang, Tianxiao [2 ]
机构
[1] Qilu Univ Technol, Shandong Acad Sci, Sch Chem & Chem Engn, 3501 Da Xue Rd, Jinan 250353, Peoples R China
[2] Fudan Univ, Huashan Hosp, Dept Pharm, 108 Luxiang Rd, Shanghai 201907, Peoples R China
基金
中国国家自然科学基金;
关键词
ERR & gamma; modulators; signaling pathways; agonists; inverse agonists; structure-activity relationship; residue; 4-HYDROXYTAMOXIFEN ANALOGS; BIOLOGICAL EVALUATION; BISPHENOL-A; ORPHAN; IDENTIFICATION; BETA; LIGAND; BINDS;
D O I
10.2174/0929867330666230518140631
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Estrogen-related receptor gamma (ERR?), one of three members of the ERR family, is an inducible transcription factor. ERR? has dual functions in different tissues. The decreased expression of ERR? in the brain, stomach, prostate, and fat cells can cause neuropsychological dysfunction, gastric cancer, prostate cancer, and obesity. However, when ERR? is present in the liver, pancreas, and thyroid follicular cells, ERR? overexpression is related to liver cancer, type II diabetes, oxidative liver injury, and anaplastic thyroid carcinoma. Signaling pathway studies have confirmed that ERR? agonists or inverse agonists can regulate ERR? expression to treat related diseases. The collision between residue Phe435 and the modulator is a key factor determining the activation or inhibition of ERR?. Although more than 20 agonists and inverse agonists of ERR? have been reported, no clinical studies have been found in the literature. This review summarizes the important relationship between ERR?-related signaling pathways and diseases, research progress, and the structure-activity relationship of modulators. These findings provide guidance for further study on new ERR? modulators.
引用
收藏
页码:3653 / 3667
页数:15
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