Dual role of autophagy in hallmarks of cancer

被引:438
|
作者
Singh, Shikha Satendra [1 ,2 ]
Vats, Somya [3 ]
Chia, Amelia Yi-Qian [2 ]
Tan, Tuan Zea [1 ]
Deng, Shuo [4 ]
Ong, Mei Shan [4 ]
Arfuso, Frank [5 ]
Yap, Celestial T. [4 ]
Goh, Boon Cher [1 ,2 ,6 ,7 ]
Sethi, Gautam [2 ,8 ]
Huang, Ruby Yun-Ju [1 ,9 ,10 ]
Shen, Han Ming [4 ,11 ]
Manjithaya, Ravi [3 ]
Kumar, Alan Prem [1 ,2 ,7 ,12 ,13 ]
机构
[1] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore, Singapore
[3] Jawaharlal Nehru Ctr Adv Sci Res, Mol Biol & Genet Unit, Bengaluru, Karnataka, India
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore, Singapore
[5] Curtin Univ, Curtin Hlth Innovat Res Inst, Sch Biomed Sci, Stem Cell & Canc Biol Lab, Perth, WA, Australia
[6] Natl Univ Hlth Syst, Natl Univ Hosp, Dept Haematol Oncol, Singapore, Singapore
[7] Natl Univ Hlth Syst, Natl Univ Canc Inst, Singapore, Singapore
[8] Curtin Univ, Curtin Hlth Innovat Res Inst, Sch Biomed Sci, Perth, WA, Australia
[9] Natl Univ Hlth Syst, Dept Obstet & Gynaecol, Singapore, Singapore
[10] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Anat, Singapore, Singapore
[11] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn, Singapore, Singapore
[12] Curtin Univ, Curtin Med Sch, Fac Hlth Sci, Perth, WA, Australia
[13] Natl Univ Singapore, Yong Loo Lin Sch Med, Med Sci Cluster, Singapore, Singapore
基金
英国医学研究理事会; 英国惠康基金;
关键词
HYPOXIA-INDUCED AUTOPHAGY; CELL-DEATH; EPIGENETIC REGULATION; LC3; CONJUGATION; COMPLEX; INHIBITION; INDUCTION; BECLIN-1; STRESS; TUMORIGENESIS;
D O I
10.1038/s41388-017-0046-6
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
Evolutionarily conserved across eukaryotic cells, macroautophagy (herein autophagy) is an intracellular catabolic degradative process targeting damaged and superfluous cellular proteins, organelles, and other cytoplasmic components. Mechanistically, it involves formation of double-membrane vesicles called autophagosomes that capture cytosolic cargo and deliver it to lysosomes, wherein the breakdown products are eventually recycled back to the cytoplasm. Dysregulation of autophagy often results in various disease manifestations, including neurodegeneration, microbial infections, and cancer. In the case of cancer, extensive attention has been devoted to understanding the paradoxical roles of autophagy in tumor suppression and tumor promotion. In this review, while we summarize how this self-eating process is implicated at various stages of tumorigenesis, most importantly, we address the link between autophagy and hallmarks of cancer. This would eventually provide a better understanding of tumor dependence on autophagy. We also discuss how therapeutics targeting autophagy can counter various transformations involved in tumorigenesis. Finally, this review will provide a novel insight into the mutational landscapes of autophagy-related genes in several human cancers, using genetic information collected from an array of cancers.
引用
收藏
页码:1142 / 1158
页数:17
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