TRG Oncology, Global Drug Discovery, Bayer HealthCare, D-13342 Berlin, Germany.
Mol Cell Endocrinol. 2012 Apr 16;352(1-2):79-91. doi: 10.1016/j.mce.2011.06.002. Epub 2011 Jun 16.
The androgens testosterone and dihydrotestosterone play an essential role in the development and maintenance of primary and secondary male characteristics. Androgens bind to a specific androgen receptor (AR), a ligand-dependent transcription factor which controls the expression of a large number of downstream target genes. The AR is an essential player in early and late prostate cancer, and may also be involved in some forms of breast cancer. It also represents a drug target for the treatment of hypogonadism. Recent studies furthermore indicate that targeting the AR in pathologies such as frailty syndrome, cachexia or polycystic ovary syndrome may have clinical benefit. Numerous AR ligands with very different pharmacological properties have been identified in the last 40 years and helped to treat several of these diseases. However, progress still needs to be made in order to find compounds with an improved profile with regard to efficacy, differentiation and side-effects. This will only be achieved through a better understanding of the mechanisms involved in normal and aberrant AR signaling.
雄激素睾酮和二氢睾酮在男性第一性征和第二性征的发育和维持中起着至关重要的作用。雄激素与特定的雄激素受体(AR)结合,AR 是一种配体依赖性转录因子,可控制大量下游靶基因的表达。AR 是早期和晚期前列腺癌的关键因素,也可能与某些形式的乳腺癌有关。它也是治疗性腺功能减退症的药物靶点。最近的研究还表明,针对脆弱综合征、恶病质或多囊卵巢综合征等疾病中的 AR 可能具有临床益处。在过去的 40 年中,已经鉴定出许多具有非常不同药理学特性的 AR 配体,这些配体有助于治疗其中的一些疾病。然而,要找到在疗效、分化和副作用方面具有改善特征的化合物,仍需要取得进展。这只有通过更好地了解正常和异常 AR 信号转导所涉及的机制才能实现。