The Role of Autophagy in Liver Cancer: Crosstalk in Signaling Pathways and Potential Therapeutic Targets

被引:68
作者
Cui, Jianzhou [1 ,2 ]
Shen, Han-Ming [1 ,3 ]
Lim, Lina Hsiu Kim [1 ,2 ,4 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore 117593, Singapore
[2] Natl Univ Singapore, Life Sci Inst, NUS Immunol Program, Singapore 117456, Singapore
[3] Univ Macau, Fac Hlth Sci, Macau, Peoples R China
[4] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn, Singapore 119077, Singapore
基金
英国医学研究理事会;
关键词
autophagy; HCC; ULK1; mTOR; AMPK; MAPK; p53; HEPATOCELLULAR-CARCINOMA CELL; NF-KAPPA-B; ACTIVATED PROTEIN-KINASE; BETA-CATENIN; PI3K/AKT/MTOR PATHWAY; POOR-PROGNOSIS; MALIGNANT PHENOTYPE; INHIBITS AUTOPHAGY; ENHANCES AUTOPHAGY; PROMOTES AUTOPHAGY;
D O I
10.3390/ph13120432
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Autophagy is an evolutionarily conserved lysosomal-dependent pathway for degrading cytoplasmic proteins, macromolecules, and organelles. Autophagy-related genes (Atgs) are the core molecular machinery in the control of autophagy, and several major functional groups of Atgs coordinate the entire autophagic process. Autophagy plays a dual role in liver cancer development via several critical signaling pathways, including the PI3K-AKT-mTOR, AMPK-mTOR, EGF, MAPK, Wnt/beta-catenin, p53, and NF-kappa B pathways. Here, we review the signaling pathways involved in the cross-talk between autophagy and hepatocellular carcinoma (HCC) and analyze the status of the development of novel HCC therapy by targeting the core molecular machinery of autophagy as well as the key signaling pathways. The induction or the inhibition of autophagy by the modulation of signaling pathways can confer therapeutic benefits to patients. Understanding the molecular mechanisms underlying the cross-link of autophagy and HCC may extend to translational studies that may ultimately lead to novel therapy and regimen formation in HCC treatment.
引用
收藏
页码:1 / 27
页数:27
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