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激素应答 G 蛋白偶联受体对前列腺癌的调控。

Regulation of prostate cancer by hormone-responsive G protein-coupled receptors.

机构信息

Department of Clinical Laboratory, Xiamen Huli Guoyu Clinic, Co., Ltd., Xiamen, China.

Department of Clinical Laboratory, Xiamen Huli Guoyu Clinic, Co., Ltd., Xiamen, China.

出版信息

Pharmacol Ther. 2018 Nov;191:135-147. doi: 10.1016/j.pharmthera.2018.06.005. Epub 2018 Jun 15.

Abstract

Regulation of prostate cancer by androgen and androgen receptor (AR), and blockade of AR signaling by AR antagonists and steroidogenic enzyme inhibitors have been extensively studied. G protein-coupled receptors (GPCRs) are a family of membrane receptors that regulate almost all physiological processes. Nearly 40% of FDA-approved drugs in the market target GPCRs. A variety of GPCRs that mediate reproductive function have been demonstrated to be involved in the regulation of prostate cancer. These GPCRs include gonadotropin-releasing hormone receptor, luteinizing hormone receptor, follicle-stimulating hormone receptor, relaxin receptor, ghrelin receptor, and kisspeptin receptor. We highlight here GPCR regulation of prostate cancer by these GPCRs. Further therapeutic approaches targeting these GPCRs for the treatment of prostate cancer are summarized.

摘要

雄激素和雄激素受体(AR)对前列腺癌的调节,以及 AR 拮抗剂和甾体激素合成酶抑制剂对 AR 信号的阻断作用已得到广泛研究。G 蛋白偶联受体(GPCRs)是一类调节几乎所有生理过程的膜受体。市场上近 40%的 FDA 批准药物的靶点是 GPCRs。已经证明,多种介导生殖功能的 GPCRs 参与了前列腺癌的调控。这些 GPCR 包括促性腺激素释放激素受体、黄体生成素受体、卵泡刺激素受体、松弛素受体、ghrelin 受体和 kisspeptin 受体。在这里,我们重点介绍这些 GPCR 对前列腺癌的 GPCR 调节。总结了针对这些 GPCR 治疗前列腺癌的进一步治疗方法。

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