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黄酮哌醇,一种转录抑制剂:影响、问题与解决方案

Flavopiridol, an inhibitor of transcription: implications, problems and solutions.

作者信息

Blagosklonny Mikhail V

机构信息

Brander Cancer Research Institute, New York Medical College, New York 10532, USA.

出版信息

Cell Cycle. 2004 Dec;3(12):1537-42. doi: 10.4161/cc.3.12.1278. Epub 2004 Dec 1.

Abstract

After a decade of exciting promises, the CDK inhibitor flavopiridol has quietly failed in most clinical trials. This review discusses that flavopiridol is a potent inhibitor of global transcription. This explains not only downregulation of numerous proteins, cell cycle arrest and apoptosis but also all pleiotropic and mysterious effects of flavopiridol. Yet, flavopiridol is not just a second actinomycin D. As an inhibitor of transcription with a unique mechanism of action, flavopiridol may have tremendous clinical potentials. This article reviews the molecular and cellular effects of flavopiridol as well as mechanisms of therapeutic and side effects, suggesting its novel clinical applications as a single agent and in drug combinations.

摘要

在经历了十年令人兴奋的承诺之后,CDK抑制剂黄酮哌啶醇在大多数临床试验中悄然失败。本综述讨论了黄酮哌啶醇是一种有效的全局转录抑制剂。这不仅解释了众多蛋白质的下调、细胞周期停滞和细胞凋亡,也解释了黄酮哌啶醇所有的多效性和神秘效应。然而,黄酮哌啶醇不仅仅是第二种放线菌素D。作为一种具有独特作用机制的转录抑制剂,黄酮哌啶醇可能具有巨大的临床潜力。本文综述了黄酮哌啶醇的分子和细胞效应以及治疗和副作用机制,提出了其作为单一药物及联合用药的新临床应用。

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