Autophagic pathways as new targets for cancer drug development

被引:96
作者
Liu, Bo [1 ,2 ,3 ]
Cheng, Yan [4 ,5 ,6 ]
Liu, Qian [1 ,2 ,3 ]
Bao, Jin-ku [1 ,2 ,3 ]
Yang, Jin-Ming [4 ,5 ,6 ]
机构
[1] Sichuan Univ, Sch Life Sci, Chengdu 610064, Peoples R China
[2] Sichuan Univ, State Key Lab Biotherapy, Chengdu 610064, Peoples R China
[3] Sichuan Univ, Ctr Canc, W China Hosp, W China Med Sch, Chengdu 610064, Peoples R China
[4] Penn State Univ, Dept Pharmacol, Coll Med, Hershey, PA 17033 USA
[5] Penn State Univ, Penn State Canc Inst, Coll Med, Hershey, PA 17033 USA
[6] Milton S Hershey Med Ctr, Hershey, PA 17033 USA
关键词
autophagy; cancer; autophagy-related gene (ATG); Beclin-1; Bcl-2; Class III and I PI3K; mTOR; p53; INTERACTING FACTOR-I; PHOSPHATIDYLINOSITOL 3-KINASE COMPLEXES; TUBEROUS SCLEROSIS COMPLEX; MALIGNANT GLIOMA-CELLS; TUMOR-SUPPRESSOR GENE; PROTEIN-KINASE; DECREASED EXPRESSION; MAMMALIAN TARGET; DOWN-REGULATION; ONCOGENIC PI3K;
D O I
10.1038/aps.2010.118
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Autophagy is an evolutionarily conserved lysosomal self-digestion process involved in degradation of long-lived proteins and damaged organelles. In recent years, increasing evidence indicates that autophagy is associated with a number of pathological processes, including cancer. In this review, we focus on the recent studies of the evolutionarily conserved autophagy-related genes (ATGs) that are implicated in autophagosome formation and the pathways involved. We discuss several key autophagic mediators (eg, Beclin-1, UVRAG, Bcl-2, Class III and I PI3K, mTOR, and p53) that play pivotal roles in autophagic signaling networks in cancer. We discuss the Janus roles of autophagy in cancer and highlighted their relationship to tumor suppression and tumor progression. We also present some examples of targeting ATGs and several protein kinases as anticancer strategy, and discuss some autophagy-modulating agents as antitumor agents. A better understanding of the relationship between autophagy and cancer would ultimately allow us to harness autophagic pathways as new targets for drug discovery in cancer therapeutics.
引用
收藏
页码:1154 / 1164
页数:11
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