小分子
RNA干扰
信号转导
拟肽
车站3
药物发现
计算生物学
化学
细胞信号
生物
细胞生物学
核糖核酸
生物化学
基因
肽
作者
Jinxia Deng,Fedora Grande,Nouri Neamati
出处
期刊:Current Cancer Drug Targets
[Bentham Science]
日期:2007-02-01
卷期号:7 (1): 91-107
被引量:120
标识
DOI:10.2174/156800907780006922
摘要
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.
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