Autophagy signaling and the cogwheels of cancer

被引:133
作者
Botti, Joelle [1 ]
Djavaheri-Mergny, Mojgan [1 ]
Pilatte, Yannick [1 ]
Codogno, Patrice [1 ]
机构
[1] Univ Paris Sud, U756, Fac Pharm, INSERM, F-92296 Chatenay Malabry, France
关键词
macroautophagy; signal transduction; proliferation; cell growth; cell survival; cell death; minor immunity;
D O I
10.4161/auto.2.2.2458
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The downregulation of macroautophagy observed in cancer cells is associated with tumor progression. The regulation of macroautophagy by signaling pathways overlaps with the control of cell growth, proliferation, cell survival and death. Several tumor suppressor genes (PTEN, TSC2 and p53) involved in the mTOR signaling network have been shown to stimulate autophagy. In contrast, the oncoproteins involved in this network have the opposite effect. These findings, together with the discovery that haploinsufficiency of the tumor suppressor beclin 1 promotes tumorigenesis in various tissues in transgenic mice, give credibility to the idea that autophagy is a tumor suppressor mechanism. The induction of macroautophagy by cancer treatments may also contribute to cell eradication. However, cancer cells sometimes mobilize autophogic capacities in response to various stimuli without a fatal outcome, suggesting that they can also exploit macroautophagy for their own benefit.
引用
收藏
页码:67 / 73
页数:7
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