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选择性雄激素受体调节剂的研发及其治疗应用。

Development of selective androgen receptor modulators and their therapeutic applications.

作者信息

Chen Fang, Rodan Gideon A, Schmidt Azi

机构信息

Department of Bone Biology & Osteoporosis Research, Merck Research Laboratories, Merck & Co, Inc., WP26A-1000 West Point, PA 19486, USA.

出版信息

Zhonghua Nan Ke Xue. 2002;8(3):162-8.

Abstract

Androgens control a broad range of physiological functions. The androgen receptor (AR), a steroid receptor that mediates the diverse biological actions of androgens, is a ligand inducible transcription factor. Abnormalities in the androgen signaling system result in many disturbances ranging from changes in gender determination and sexual development to psychiatric and emotional disorders. Androgen replacement therapy can improve many clinical conditions including hypogonadism and osteoporosis, but is limited by the lack of efficacious and safe therapeutic agents with easy delivery options. Recent progress in the area of gene regulation by steroid receptors and by selective receptor modulators provides an opportunity to examine if selective androgen receptor modulators (SARMs) could address some of the problems associated with current androgen therapy. Since the composition of the transcriptional initiation complex recruited by liganded AR determines the specificity of gene regulation, synthetic ligands aimed at initiating transcription of tissue and promoter specific genes offers hope for developing better androgen therapy. Establishment of assays that predict synthetic ligand activity is critical for SARM development. Advancement in high throughput compound screening and gene fingerprinting technologies, such as microarrays and proteomics, will facilitate and accelerate identification of effective SARMs.

摘要

雄激素控制着广泛的生理功能。雄激素受体(AR)是一种介导雄激素多种生物学作用的类固醇受体,是一种配体诱导型转录因子。雄激素信号系统的异常会导致许多紊乱,从性别决定和性发育的变化到精神和情绪障碍。雄激素替代疗法可以改善包括性腺功能减退和骨质疏松症在内的许多临床病症,但由于缺乏有效且安全、给药方式简便的治疗药物而受到限制。类固醇受体和选择性受体调节剂在基因调控领域的最新进展为研究选择性雄激素受体调节剂(SARM)是否能够解决当前雄激素治疗相关的一些问题提供了契机。由于与配体结合的AR招募的转录起始复合物的组成决定了基因调控的特异性,旨在启动组织和启动子特异性基因转录的合成配体为开发更好的雄激素疗法带来了希望。建立预测合成配体活性的检测方法对于SARM的开发至关重要。高通量化合物筛选和基因指纹技术(如微阵列和蛋白质组学)的进步将促进并加速有效SARM的鉴定。

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