Dai Yun, Grant Steven
Department of Medicine, Virginia Commonwealth University and Massey Cancer Center, Richmond, Virginia, USA.
Cancer Res. 2007 Apr 1;67(7):2908-11. doi: 10.1158/0008-5472.CAN-07-0082.
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.
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。