Non-canonical autophagy

被引:65
作者
Scarlatti, Francesca [1 ]
Maffei, Roberta [2 ]
Beau, Isabelle [3 ]
Ghidoni, Riccardo [2 ]
Codogno, Patrice [3 ]
机构
[1] Univ Turin, Lab Cellular & Mol Endocrinol, Div Endocrinol & Metab, Dept Internal Med, I-10126 Turin 14, Italy
[2] Univ Milan, San Paolo Univ Hosp Med Sch, Biochem & Mol Biol Lab, Milan, Italy
[3] Univ Paris 11, INSERM, U756, Chatenay Malabry, France
关键词
beclin; 1; hvps34; caspase-independent cell death; reveratrol; breast cancer; macroautophagy;
D O I
10.4161/auto.7068
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Macroautophagy (hereafter called autophagy) is a dynamic and evolutionarily conserved process used to sequester and degrade cytoplasm and entire organelles in a sequestering vesicle with a double membrane, known as the autophagosome, which ultimately fuses with a lysosome to degrade its autophagic cargo. Recently, we have unraveled two distinct forms of autophagy in cancer cells, which we term canonical and non-canonical autophagy. In contrast to classical or canonical autophagy, non-canonical autophagy is a process that does not require the entire set of autophagy-related (Atg) proteins in particular Beclin 1, to form the autophagosome. Non-canonical autophagy is therefore not blocked by the knockdown of Beclin I or of its binding partner hVps34. Moreover overexpression of Bcl-2, which is known to block canonical starvation-induced autophagy by binding to Beclin 1, is unable to reverse the non-canonical autophagy triggered by the polyphenol resveratrol in the breast cancer MCF-7 cell line. In MCF-7 cells, at least, non-canonical autophagy is involved in the caspase-independent cell death induced by resveratrol.
引用
收藏
页码:1083 / 1085
页数:3
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