The Bcl-2 family: roles in cell survival and oncogenesis

被引:1231
作者
Cory, S [1 ]
Huang, DCS [1 ]
Adams, JM [1 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
关键词
apoptosis; caspases; oncogenesis; mouse models; therapeutics;
D O I
10.1038/sj.onc.1207102
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis, the cell-suicide programme executed by caspases, is critical for maintaining tissue homeostasis, and impaired apoptosis is now recognized to be a key step in tumorigenesis. Whether a cell should live or die is largely determined by the Bcl-2 family of anti- and proapoptotic regulators. These proteins respond to cues from various forms of intracellular stress, such as DNA damage or cytokine deprivation, and interact with opposing family members to determine whether or not the caspase proteolytic cascade should be unleashed. This review summarizes current views of how these proteins sense stress, interact with their relatives, perturb organelles such as the mitochondrion and endoplasmic reticulum and govern pathways to caspase activation. It briefly explores how family members influence cell-cycle entry and outlines the evidence for their involvement in tumour development, both as oncoproteins and tumour suppressors. Finally, it discusses the promise of novel anticancer therapeutics that target these vital regulators.
引用
收藏
页码:8590 / 8607
页数:18
相关论文
共 309 条
[41]   BAD and glucokinase reside in a mitochondrial complex that integrates glycolysis and apoptosis [J].
Danial, NN ;
Gramm, CF ;
Scorrano, L ;
Zhang, CY ;
Krauss, S ;
Ranger, AM ;
Datta, SR ;
Greenberg, ME ;
Licklider, LJ ;
Lowell, BB ;
Gygi, SP ;
Korsmeyer, SJ .
NATURE, 2003, 424 (6951) :952-956
[42]   A decade of caspases [J].
Degterev, A ;
Boyce, M ;
Yuan, JY .
ONCOGENE, 2003, 22 (53) :8543-8567
[43]   Identification of small-molecule inhibitors of interaction between the BH3 domain and Bcl-xL [J].
Degterev, A ;
Lugovskoy, A ;
Cardone, M ;
Mulley, B ;
Wagner, G ;
Mitchison, T ;
Yuan, JY .
NATURE CELL BIOLOGY, 2001, 3 (02) :173-182
[44]  
del Peso L, 2000, J BIOL CHEM, V275, P27205
[45]   Phosphorylation of bid by casein kinases I and II regulates its cleavage by caspase 8 [J].
Desagher, S ;
Osen-Sand, A ;
Montessuit, S ;
Magnenat, E ;
Vilbois, F ;
Hochmann, A ;
Journot, L ;
Antonsson, B ;
Martinou, JC .
MOLECULAR CELL, 2001, 8 (03) :601-611
[46]   FKHR-L1 can act as a critical effector of cell death induced by cytokine withdrawal: protein kinase B-enhanced cell survival through maintenance of mitochondrial integrity [J].
Dijkers, PF ;
Birkenkamp, KU ;
Lam, EWF ;
Thomas, NSB ;
Lammers, JWJ ;
Koenderman, L ;
Coffer, PJ .
JOURNAL OF CELL BIOLOGY, 2002, 156 (03) :531-542
[47]   Expression of the pro-apoptotic Bcl-2 family member Bim is regulated by the forkhead transcription factor FKHR-L1 [J].
Dijkers, PF ;
Medema, RH ;
Lammers, JWJ ;
Koenderman, L ;
Coffer, PJ .
CURRENT BIOLOGY, 2000, 10 (19) :1201-1204
[48]   Perspectives on the development of a molecularly targeted agent [J].
Druker, BJ .
CANCER CELL, 2002, 1 (01) :31-36
[49]   Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition [J].
Du, CY ;
Fang, M ;
Li, YC ;
Li, L ;
Wang, XD .
CELL, 2000, 102 (01) :33-42
[50]   Mammalian caspases: Structure, activation, substrates, and functions during apoptosis [J].
Earnshaw, WC ;
Martins, LM ;
Kaufmann, SH .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :383-424