Department of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, University at Buffalo SUNY, 543 Cooke Hall, Buffalo, NY 14260, USA.
Adv Drug Deliv Rev. 2010 Oct 30;62(13):1277-84. doi: 10.1016/j.addr.2010.08.002. Epub 2010 Aug 12.
Androgens function as sex hormone primarily via activation of a single androgen receptor (AR, or NR3C4). AR is an important therapeutic target for the treatment of diseases such as hypogonadism and prostate cancer. AR ligands of different chemical structures and/or pharmacological properties are widely used for these therapeutic applications, and all of the AR ligands currently available for therapy modulate AR function via direct binding to the ligand-binding pocket (LBP) of the receptor. In the past ten years, our understanding of AR structure and molecular mechanism of action has progressed extensively, which has encouraged the rapid development of newer generation of AR ligands, particularly tissue-selective AR ligands. With improved tissue selectivity, future generations of AR ligands are expected to greatly expand the therapeutic applications of this class of drugs. This review will provide an overview of the common therapeutic applications of currently available AR ligands, and discussion of the major challenges as well as novel therapeutic strategies proposed for future drug development.
雄激素主要通过激活单一的雄激素受体 (AR,或 NR3C4) 发挥其作为性激素的作用。AR 是治疗低促性腺激素血症和前列腺癌等疾病的重要治疗靶点。具有不同化学结构和/或药理特性的 AR 配体被广泛用于这些治疗应用,目前可用于治疗的所有 AR 配体均通过直接结合受体的配体结合口袋 (LBP) 来调节 AR 功能。在过去的十年中,我们对 AR 结构和作用机制的认识有了很大的进展,这鼓励了新一代 AR 配体的快速发展,特别是组织选择性 AR 配体。随着组织选择性的提高,未来几代的 AR 配体有望极大地扩展这类药物的治疗应用。本文将概述目前可用的 AR 配体的常见治疗应用,并讨论未来药物开发中提出的主要挑战和新的治疗策略。