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Development of selective androgen receptor modulators (SARMs)

机译:开发选择性雄激素受体调节剂(SARMS)

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The Androgen Receptor (AR), a member of the steroid hormone receptor family, plays important roles in the physiology and pathology of diverse tissues. AR ligands, which include circulating testosterone and locally synthesized dihydrotestosterone, bind to and activate the AR to elicit their effects. Ubiquitous expression of the AR, metabolism and cross reactivity with other receptors limit broad therapeutic utilization of steroidal androgens. However, the discovery of selective androgen receptor modulators (SARMs) and other tissue-selective nuclear hormone receptor modulators that activate their cognate receptors in a tissue-selective manner provides an opportunity to promote the beneficial effects of androgens and other hormones in target tissues with greatly reduced unwanted side-effects. In the last two decades, significant resources have been dedicated to the discovery and biological characterization of SARMs in an effort to harness the untapped potential of the AR. SARMs have been proposed as treatments of choice for various diseases, including muscle-wasting, breast cancer, and osteoporosis. This review provides insight into the evolution of SARMs from proof-of-concept agents to the cusp of therapeutic use in less than two decades, while covering contemporary views of their mechanisms of action and therapeutic benefits. (C) 2017 Elsevier B.V. All rights reserved.
机译:雄激素受体(AR)是类固醇激素受体家庭的成员,在不同组织的生理和病理学中起重要作用。 Ar配体,包括循环睾酮和局部合成的二氢酮,结合并激活AR以引发其效果。与其他受体的AR,代谢和交叉反应性的无处不在的表达限制了甾体雄激素的广泛治疗利用率。然而,选择性雄激素受体调节剂(SARMS)和其他组织选择性核激素受体调节剂,其以组织可选择的方式激活其同源受体,提供了促进雌激素和其他激素在靶组织中的有益作用的机会减少了不必要的副作用。在过去的二十年中,大量资源致力于努力利用AR的未开发的潜力来努力解决SARM的发现和生物学特征。已经提出了SARMS作为各种疾病的选择的治疗,包括肌肉浪费,乳腺癌和骨质疏松症。本综述介绍了在不到二十年的时间内从概念证明代理人对概念验证的演变的洞察力,同时涵盖了对其行动和治疗福利机制的当代观点。 (c)2017 Elsevier B.v.保留所有权利。

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