Apoptosis and oncogenesis: give and take in the BCL-2 family

被引:217
作者
Llambi, Fabien [1 ]
Green, Douglas R. [1 ]
机构
[1] St Jude Childrens Hosp, Dept Immunol, Memphis, TN USA
关键词
MITOCHONDRIAL-MEMBRANE PERMEABILIZATION; INDEPENDENT CELL-DEATH; LIPIDIC PORE FORMATION; MYC-INDUCED APOPTOSIS; TUMOR-SUPPRESSOR P53; BH3 MIMETIC ABT-737; E3 UBIQUITIN LIGASE; BAX ACTIVATION; DNA-DAMAGE; TRANSGENIC MICE;
D O I
10.1016/j.gde.2010.12.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mitochondrial pathway of apoptosis constitutes one of the main safeguards against tumorigenesis. The BCL-2 family includes the central players of this pathway that regulate cell fate through the control of mitochondrial outer membrane permeabilization (MOMP), and important progress has been made in understanding the dynamic interactions between proapoptotic and anti-apoptotic BCL-2 proteins. In particular, recent studies have delineated a stepwise model for the induction of MOMP. BCL-2 proteins are often dysregulated in cancer, leading to increased survival of abnormal cells; however, recent studies have paradoxically shown that apoptosis induction can under some circumstances drive tumor formation, perhaps by inducing compensatory proliferation under conditions of cellular stress. These observations underline the complexity of BCL-2 protein function in oncogenesis.
引用
收藏
页码:12 / 20
页数:9
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