Department of Global Discovery Chemistry, Novartis Institutes for Biomedical Research, 250 Massachusetts Avenue, Cambridge, MA 02139, USA.
ChemMedChem. 2010 Apr 6;5(4):500-12. doi: 10.1002/cmdc.201000011.
Inhibitors of the Hedgehog (Hh) molecular signaling pathway have emerged in recent years as a promising new class of potential therapeutics for cancer treatment. Numerous drug discovery efforts have resulted in the identification of a wide variety of small molecules that target different members of this pathway, including Smoothened (Smo), Sonic hedgehog protein (Shh), and Gli1. Several Smo inhibitors have now entered human clinical trials, and successful proof-of-concept studies have been carried out in patients with defined genetic mutations in the Hh pathway. This review provides a general overview of three main topics in this rapidly expanding area: 1) the various types of biological assays and in vivo models that have been employed for the identification and optimization of Hh pathway inhibitors; 2) Smo inhibitors reported to date, including recent clinical results where available; and 3) efforts toward the identification and characterization of inhibitors of other members of the Hh pathway.
近年来, Hedgehog(Hh)分子信号通路的抑制剂作为癌症治疗的一种有前途的新类别的潜在治疗药物而出现。大量的药物发现工作已经确定了广泛的靶向该途径不同成员的小分子,包括 Smoothened(Smo)、 Sonic hedgehog 蛋白(Shh)和 Gli1。现在已经有几种 Smo 抑制剂进入人体临床试验,并且在 Hh 途径中具有明确遗传突变的患者中进行了成功的概念验证研究。本综述提供了这一快速发展领域的三个主要主题的概述:1)用于鉴定和优化 Hh 途径抑制剂的各种类型的生物学测定法和体内模型;2)迄今为止报道的 Smo 抑制剂,包括可获得的最新临床结果;3)努力鉴定和表征 Hh 途径其他成员的抑制剂。