The Double-Edged Sword of Autophagy Modulation in Cancer

被引:934
作者
White, Eileen [1 ,2 ]
DiPaola, Robert S. [1 ,3 ]
机构
[1] Canc Inst New Jersey, New Brunswick, NJ 08903 USA
[2] Rutgers State Univ, Dept Mol Biol & Biochem, Piscataway, NJ 08855 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Internal Med, Div Med Oncol, New Brunswick, NJ USA
基金
美国国家卫生研究院;
关键词
UBIQUITIN-PROTEASOME SYSTEM; CELL-DEATH; REGULATES AUTOPHAGY; METABOLIC STRESS; PROSTATE-CANCER; MOUSE MODELS; APOPTOSIS; INHIBITION; TUMORIGENESIS; DEGRADATION;
D O I
10.1158/1078-0432.CCR-07-5023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Macroautophagy (autophagy) is a lysosomal degradation pathway for the breakdown of intracellular proteins and organelles. Although constitutive autophagy is a homeo-static mechanism for intracellular recycling and metabolic regulation, autophagy is also stress responsive, in which it is important for the removal of damaged proteins and organelles. Autophagy thereby confers stress tolerance, limits damage, and sustains viability under adverse conditions. Autophagy is a tumor-suppression mechanism, yet it enables tumor cell survival in stress. Reconciling how loss of a prosurvival function can promote tumorigenesis, emerging evidence suggests that preservation of cellular fitness by autophagy may be key to tumor suppression. As autophagy is such a fundamental process, establishing how the functional status of autophagy influences tumorigenesis and treatment response is important. This is especially critical as many current cancer therapeutics activate autophagy. Therefore, efforts to understand and modulate the autophagy pathway will provide new approaches to cancer therapy and prevention. (Clin Cancer Res 2009;15(17):5308-16)
引用
收藏
页码:5308 / 5316
页数:9
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