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靶向凋亡调控机制的多个环节。

Targeting multiple arms of the apoptotic regulatory machinery.

作者信息

Dai Yun, Grant Steven

机构信息

Department of Medicine, Virginia Commonwealth University and Massey Cancer Center, Richmond, Virginia, USA.

出版信息

Cancer Res. 2007 Apr 1;67(7):2908-11. doi: 10.1158/0008-5472.CAN-07-0082.

Abstract

ABT-737 targets Bcl-2/Bcl-xL but not Mcl-1, which confers resistance to this novel agent. Here, we summarize recent findings indicating that Mcl-1 represents a critical determinant of ABT-737 sensitivity and resistance, and that Mcl-1 down-regulation by various pharmacologic agents or genetic approaches dramatically increases ABT-737 lethality in diverse malignant cell types. These findings also show that the multidomain proapoptotic proteins Bax and Bak play important functional roles in ABT-737-mediated apoptosis, and that Bak activation is essential in potentiation of ABT-737 lethality by agents that down-regulate Mcl-1. Collectively, these findings suggest a novel therapeutic strategy targeting multiple arms of the apoptotic machinery.

摘要

ABT-737作用于Bcl-2/Bcl-xL而非Mcl-1,这使得肿瘤细胞对这种新型药物产生耐药性。在此,我们总结了近期的研究发现,表明Mcl-1是决定ABT-737敏感性和耐药性的关键因素,并且通过各种药理学试剂或基因方法下调Mcl-1可显著增强ABT-737对多种恶性细胞类型的致死性。这些发现还表明,多结构域促凋亡蛋白Bax和Bak在ABT-737介导的细胞凋亡中发挥重要功能作用,并且Bak激活对于下调Mcl-1的试剂增强ABT-737致死性至关重要。总体而言,这些发现提示了一种针对凋亡机制多个环节的新型治疗策略。

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