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PARP 抑制剂:多靶性与选择性抑制。

PARP inhibitors: polypharmacology versus selective inhibition.

机构信息

Karolinska Institutet, Department of Medical Biochemistry and Biophysics, Stockholm, Sweden.

出版信息

FEBS J. 2013 Aug;280(15):3563-75. doi: 10.1111/febs.12298. Epub 2013 May 24.

Abstract

Inhibition of ADP-ribosyltransferases with diphtheria toxin homology (ARTD), widely known as the poly(ADP-ribose) polymerase (PARP) family, is a strategy under development for treatment of various conditions, including cancers and ischemia. Here, we give a brief summary of ARTD enzyme functions and the implications for their potential as therapeutic targets. We present an overview of the PARP inhibitors that have been used in clinical trials. Finally, we summarize recent insights from structural biology, and discuss the molecular aspects of PARP inhibitors in terms of broad-range versus selective inhibition of ARTD family enzymes.

摘要

抑制二聚体毒素同源(ARTD)的 ADP-核糖基转移酶,通常被称为多聚(ADP-核糖)聚合酶(PARP)家族,是一种正在开发的用于治疗各种疾病的策略,包括癌症和缺血。在这里,我们简要总结了 ARTD 酶的功能及其作为治疗靶点的潜在意义。我们介绍了已在临床试验中使用的 PARP 抑制剂。最后,我们总结了结构生物学的最新研究进展,并讨论了 PARP 抑制剂在广谱和选择性抑制 ARTD 家族酶方面的分子方面。

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