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首页> 外文期刊>Molecular and Cellular Endocrinology >Haendler, B., Cleve, A.Recent developments in antiandrogens and selective androgen receptor modulators
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Haendler, B., Cleve, A.Recent developments in antiandrogens and selective androgen receptor modulators

机译:Haendler,B.,Cleve,A.抗雄激素和选择性雄激素受体调节剂的最新进展

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摘要

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.
机译:雄激素睾丸激素和二氢睾丸激素在发展和维持男性原发性和继发性男性特征中起重要作用。雄激素与特异性雄激素受体(AR)结合,后者是控制大量下游靶基因表达的依赖配体的转录因子。 AR是早期和晚期前列腺癌的重要角色,也可能参与某些形式的乳腺癌。它还代表了治疗性腺功能减退的药物靶标。最近的研究进一步表明,针对诸如衰弱综合症,恶病质或多囊卵巢综合症等病理学的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的药理特性的AR配体,并有助于治疗其中的几种疾病。然而,为了找到在功效,分化和副作用方面具有改善的特征的化合物,仍需要取得进展。只有更好地了解正常和异常AR信令所涉及的机制,才能实现这一点。

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