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用于癌症治疗的抗Bcl-2非肽类小分子抑制剂。

Non-peptidic small molecule inhibitors against Bcl-2 for cancer therapy.

作者信息

Azmi Asfar S, Mohammad Ramzi M

机构信息

Department of Pathology, Wayne State University School of Medicine, Detroit Michigan, USA.

出版信息

J Cell Physiol. 2009 Jan;218(1):13-21. doi: 10.1002/jcp.21567.

Abstract

A critical regulator of the apoptotic machinery is the Bcl-2 family proteins whose over expression confers a protective effect on malignant cells against death signals of apoptosis. Cancer cells that are resistant to various anti-cancer drugs and treatment regimen are found to over express these Bcl-2 proteins such as Bcl-2, Bcl-X(L), Mcl-1, Bcl-w, and A1/Bfl1. In recent years there has been an exponential growth in the identification as well as synthesis of non-peptidic cell permeable small-molecule inhibitors (SMIs) of protein-protein interaction. The focus of this article is on inhibitors of anti-apoptotic protein Bcl-2. This review summarizes an up to date knowledge of the available SMIs, their mode of action as well as their current status in preclinical as well as clinical development.

摘要

凋亡机制的一个关键调节因子是Bcl-2家族蛋白,其过度表达赋予恶性细胞对凋亡死亡信号的保护作用。对各种抗癌药物和治疗方案耐药的癌细胞被发现过度表达这些Bcl-2蛋白,如Bcl-2、Bcl-X(L)、Mcl-1、Bcl-w和A1/Bfl1。近年来,非肽类细胞可渗透小分子抑制剂(SMIs)的蛋白质-蛋白质相互作用的鉴定和合成呈指数增长。本文重点关注抗凋亡蛋白Bcl-2的抑制剂。本综述总结了现有SMIs的最新知识、它们的作用模式以及它们在临床前和临床开发中的现状。

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