Targeting autophagy in colorectal cancer: An update on pharmacological small-molecule compounds

被引:12
|
作者
Li, Zixiang [1 ]
Si, Wen [2 ,3 ]
Jin, Wenke [1 ]
Yuan, Zhaoxin [1 ]
Chen, Yi [4 ]
Fu, Leilei [1 ]
机构
[1] Southwest Jiaotong Univ, Sichuan Engn Res Ctr Biomimet Synth Nat Drugs, Sch Life Sci & Engn, Chengdu 610031, Peoples R China
[2] Chinese Acad Sci Ltd, Hong Kong Inst Sci & Innovat, Ctr Regenerat Med & Hlth, Hong Kong, Peoples R China
[3] City Univ Hong Kong, Dept Neurosci, Kowloon Tong, Hong Kong, Peoples R China
[4] Sichuan Univ, West China Hosp, Dept Gastrointestinal Surg, Chengdu 610041, Peoples R China
关键词
Autophagy; Colorectal cancer; Small-molecule compound; Cytoprotective autophagy; Autophagy-associated; cell death; CYCLE ARREST; CELL-DEATH; APOPTOSIS; GROWTH; MODULATION; AXIS;
D O I
10.1016/j.drudis.2022.05.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Autophagy, an evolutionarily highly conserved cellular degradation process, plays the Janus role (either cytoprotective or death-promoting) in colorectal cancer, so the targeting of several key autophagic pathways with small-molecule compounds may be a new therapeutic strategy. In this review, we discuss autophagy-associated cell death pathways and key cytoprotective autophagy pathways in colorectal cancer. Moreover, we summarize a series of small-molecule compounds that have the potential to modulate autophagy-associated cell death or cytoprotective autophagy for therapeutic purposes. Taken together, these findings demonstrate the Janus role of autophagy in colorectal cancer, and shed new light on the exploitation of a growing number of small-molecule compounds to target autophagy in future cancer drug discovery.
引用
收藏
页码:2373 / 2385
页数:13
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