The role of autophagy in tumour development and cancer therapy

被引:160
作者
Rosenfeldt, Mathias T. [1 ]
Ryan, Kevin M. [1 ]
机构
[1] Beatson Inst Canc Res, Tumour Cell Death Lab, Glasgow G61 1BD, Lanark, Scotland
来源
EXPERT REVIEWS IN MOLECULAR MEDICINE | 2009年 / 11卷
关键词
PROGRAMMED CELL-DEATH; BCL-X-L; REGULATES AUTOPHAGY; BECLIN; COLON-CANCER; PHOSPHATIDYLINOSITOL; 3-KINASE; MICROSATELLITE INSTABILITY; EMBRYONIC-DEVELOPMENT; CONJUGATION SYSTEMS; INTERACTING PROTEIN;
D O I
10.1017/S1462399409001306
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
Autophagy is a catabolic membrane-trafficking process that leads to sequestration and degradation of intracellular material within lysosomes. It is executed at basal levels in every cell and promotes cellular homeostasis by regulating organelle and protein turnover. In response to various forms of cellular stress, however, the levels and cargoes of autophagy can be modulated. In nutrient-deprived states, for example, autophagy can be activated to degrade cargoes for cell-autonomous energy production to promote cell survival. In other contexts, in contrast, autophagy has been shown to contribute to cell death. Given these dual effects in regulating cell viability, it is no surprise that autophagy has implications in both the genesis and treatment of malignant disease. In this review, we provide a comprehensive appraisal of the way in which oncogenes and tumour suppressor genes regulate autophagy. In addition, we address the current evidence from human cancer and animal models that has aided our understanding of the role of autophagy in tumour progression. Finally, the potential for targeting autophagy therapeutically is discussed in light of the functions of autophagy at different stages of tumour progression and in normal tissues.
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页数:20
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