Cell death by autophagy: emerging molecular mechanisms and implications for cancer therapy

被引:328
作者
Fulda, S. [1 ,2 ,3 ]
Koegel, D. [4 ]
机构
[1] Goethe Univ Frankfurt, Inst Expt Canc Res Pediat, D-60528 Frankfurt, Germany
[2] German Canc Consortium DKTK, Heidelberg, Germany
[3] German Canc Res Ctr, Heidelberg, Germany
[4] Goethe Univ Hosp, Ctr Neurol & Neurosurg, Expt Neurosurg, Frankfurt, Germany
关键词
SUBEROYLANILIDE HYDROXAMIC ACID; HISTONE DEACETYLASE INHIBITOR; PROSTATE-CANCER; REGULATES AUTOPHAGY; BETULINIC ACID; UP-REGULATION; APOPTOSIS; OBATOCLAX; GX15-070; LEUKEMIA;
D O I
10.1038/onc.2014.458
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Autophagy is a tightly-regulated catabolic process of cellular self-digestion by which cellular components are targeted to lysosomes for their degradation. Key functions of autophagy are to provide energy and metabolic precursors under conditions of starvation and to alleviate stress by removal of damaged proteins and organelles, which are deleterious for cell survival. Therefore, autophagy appears to serve as a pro-survival stress response in most settings. However, the role of autophagy in modulating cell death is highly dependent on the cellular context and its extent. There is an increasing evidence for cell death by autophagy, in particular in developmental cell death in lower organisms and in autophagic cancer cell death induced by novel cancer drugs. The death-promoting and - executing mechanisms involved in the different paradigms of autophagic cell death (ACD) are very diverse and complex, but a draft scenario of the key molecular targets involved in ACD is beginning to emerge. This review provides an up-to-date and comprehensive report on the molecular mechanisms of drug-induced autophagy-dependent cell death and highlights recent key findings in this exciting field of research.
引用
收藏
页码:5105 / 5113
页数:9
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