Narayanan Ramesh, Mohler Michael L, Bohl Casey E, Miller Duane D, Dalton James T
Preclinical Research and Development, GTx, Inc., Memphis, Tennessee, USA.
Nucl Recept Signal. 2008;6:e010. doi: 10.1621/nrs.06010. Epub 2008 Nov 26.
Androgen receptor (AR) plays a critical role in the function of several organs including primary and accessory sexual organs, skeletal muscle, and bone, making it a desirable therapeutic target. Selective androgen receptor modulators (SARMs) bind to the AR and demonstrate osteo- and myo-anabolic activity; however, unlike testosterone and other anabolic steroids, these nonsteroidal agents produce less of a growth effect on prostate and other secondary sexual organs. SARMs provide therapeutic opportunities in a variety of diseases, including muscle wasting associated with burns, cancer, or end-stage renal disease, osteoporosis, frailty, and hypogonadism. This review summarizes the current standing of research and development of SARMs, crystallography of AR with SARMs, plausible mechanisms for their action and the potential therapeutic indications for this emerging class of drugs.
雄激素受体(AR)在包括主副性器官、骨骼肌和骨骼在内的多个器官的功能中起着关键作用,使其成为一个理想的治疗靶点。选择性雄激素受体调节剂(SARMs)与AR结合并表现出骨和肌肉合成代谢活性;然而,与睾酮和其他合成代谢类固醇不同,这些非甾体药物对前列腺和其他第二性器官的生长作用较小。SARMs在多种疾病中提供了治疗机会,包括与烧伤、癌症或终末期肾病相关的肌肉萎缩、骨质疏松症、身体虚弱和性腺功能减退。本综述总结了SARMs的研发现状、AR与SARMs的晶体学、其作用的可能机制以及这类新兴药物的潜在治疗适应症。