Cabeza Marisa, Sánchez-Márquez Araceli, Garrido Mariana, Silva Aylín, Bratoeff Eugene
Departamento De Sistemas Biológicos, Universidad Autónoma Metropolitana- Xochimilco Calzada Del Hueso No. 1100, México, D.F., C.P. 04960, México.
Curr Med Chem. 2016;23(8):792-815. doi: 10.2174/0929867323666160210125642.
This article summarizes the importance of different targets such as 5α-reductase, 17β-HSD, CYP17A, androgen receptor and protein kinase A for the treatment of prostate cancer and benign prostatic hyperplasia. It is a well known fact that dihydrotestosterone (DHT) is associated with the development of androgen-dependent afflictions. At the present time, several research groups are attempting to develop new steroidal and non-steroidal molecules with the purpose of inhibiting the synthesis and biological response of DHT. This review also discusses the most recent studies reported in the literature that describe the therapeutic potential of novel compounds, as well as the new drugs, principally inhibitors of 5α-reductase.
本文总结了5α-还原酶、17β-羟类固醇脱氢酶、细胞色素P450 17A1、雄激素受体和蛋白激酶A等不同靶点在前列腺癌和良性前列腺增生治疗中的重要性。众所周知,双氢睾酮(DHT)与雄激素依赖性疾病的发生有关。目前,几个研究小组正在尝试开发新的甾体和非甾体分子,以抑制DHT的合成和生物学反应。本综述还讨论了文献中报道的最新研究,这些研究描述了新型化合物以及主要为5α-还原酶抑制剂的新药的治疗潜力。