Deng Jinxia, Grande Fedora, Neamati Nouri
Department of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, 1985 Zonal Avenue, Los Angeles, CA 90089, USA.
Curr Cancer Drug Targets. 2007 Feb;7(1):91-107. doi: 10.2174/156800907780006922.
Constitutive activation of the Signal Transducers and Activators of Transcription 3 (Stat3) meditated signaling pathway is very important for cell growth and survival. Compelling evidence from mechanistic studies with antisense, RNA interference (RNAi), peptides, and small molecular inhibitors indicate that blocking Stat3 signaling can lead to successful suppression of tumor cell growth and apoptosis. Thus, Stat3 is an attractive molecular target for the development of novel cancer therapeutics. In this article, we present the first comprehensive review focusing on small molecule inhibitors that effectively block the Stat3 signaling pathway. These inhibitors, from a structural point of view, are divided into five classes of compounds. They include (1) natural products and derivatives, such as curcumin, resveratrol and others, (2) tyrphostins, (3) platinum-containing complexes, (4) peptidomimetics, and (5) azaspiranes. Some compounds may have multiple targets including Stat3 protein, therefore these compounds need further optimization and validation. The purpose of this review is to provide a resource for researchers interested in Stat3 targeted small molecules which will be beneficial for database development and template design for future drug development.
信号转导子与转录激活子3(Stat3)介导的信号通路的组成性激活对细胞生长和存活非常重要。来自反义、RNA干扰(RNAi)、肽和小分子抑制剂的机制研究的有力证据表明,阻断Stat3信号传导可成功抑制肿瘤细胞生长和凋亡。因此,Stat3是开发新型癌症治疗药物的一个有吸引力的分子靶点。在本文中,我们首次对有效阻断Stat3信号通路的小分子抑制剂进行了全面综述。从结构角度来看,这些抑制剂分为五类化合物。它们包括(1)天然产物及其衍生物,如姜黄素、白藜芦醇等,(2)酪氨酸磷酸化抑制剂,(3)含铂配合物,(4)肽模拟物,以及(5)氮杂螺烷。一些化合物可能有包括Stat3蛋白在内的多个靶点,因此这些化合物需要进一步优化和验证。本综述的目的是为对Stat3靶向小分子感兴趣的研究人员提供资源,这将有助于数据库开发和未来药物开发的模板设计。