Life and death partners: apoptosis, autophagy and the cross-talk between them

被引:1021
作者
Eisenberg-Lerner, A. [1 ]
Bialik, S. [1 ]
Simon, H-U [2 ]
Kimchi, A. [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[2] Univ Bern, Fac Med, Inst Pharmacol, CH-3010 Bern, Switzerland
基金
以色列科学基金会;
关键词
autophagy; apoptosis; tumorigenesis; PROGRAMMED CELL-DEATH; DAP-KINASE; METABOLIC STRESS; PROTEIN-KINASES; UP-REGULATION; CANCER-CELLS; BECLIN; SURVIVAL; PHOSPHORYLATION; ACTIVATION;
D O I
10.1038/cdd.2009.33
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
It is not surprising that the demise of a cell is a complex well-controlled process. Apoptosis, the first genetically programmed death process identified, has been extensively studied and its contribution to the pathogenesis of disease well documented. Yet, apoptosis does not function alone to determine a cell's fate. More recently, autophagy, a process in which de novo-formed membrane-enclosed vesicles engulf and consume cellular components, has been shown to engage in a complex interplay with apoptosis. In some cellular settings, it can serve as a cell survival pathway, suppressing apoptosis, and in others, it can lead to death itself, either in collaboration with apoptosis or as a back-up mechanism when the former is defective. The molecular regulators of both pathways are inter-connected; numerous death stimuli are capable of activating either pathway, and both pathways share several genes that are critical for their respective execution. The cross-talk between apoptosis and autophagy is therefore quite complex, and sometimes contradictory, but surely critical to the overall fate of the cell. Furthermore, the crosstalk is a key factor in the outcome of death-related pathologies such as cancer, its development and treatment. Cell Death and Differentiation (2009) 16, 966-975; doi: 10.1038/cdd.2009.33; published online 27 March 2009
引用
收藏
页码:966 / 975
页数:10
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