Autophagy and liver cancer

被引:66
作者
Chao, Xiaojuan [1 ]
Qian, Hui [1 ]
Wang, Shaogui [1 ]
Fulte, Sam [1 ]
Ding, Wen-Xing [1 ]
机构
[1] Univ Kansas, Dept Pharmacol Toxicol & Therapeut, Med Ctr, MS 1018,3901 Rainbow Blvd, Kansas City, KS 66160 USA
关键词
Alcohol; mTOR; Nrf2; p62; TFEB; ENDOPLASMIC-RETICULUM STRESS; PANCREATIC STELLATE CELLS; TRANSCRIPTION FACTOR NRF2; HEPATITIS-B-VIRUS; PROTEIN-KINASE-C; HEPATOCELLULAR-CARCINOMA; TUMOR-SUPPRESSOR; OXIDATIVE STRESS; PERSISTENT ACTIVATION; KEAP1-NRF2; PATHWAY;
D O I
10.3350/cmh.2020.0169
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Autophagy is a highly conserved catabolic process that degrades cytosolic proteins and organelles via formation of autophagosomes that fuse with lysosomes to form autolysosomes, whereby autophagic cargos are degraded. Numerous studies have demonstrated that autophagy plays a critical role in the regulation of liver physiology and homeostasis, and impaired autophagy leads to the pathogenesis of various liver diseases such as viral hepatitis, alcohol associated liver diseases (AALD), non-alcoholic fatty liver diseases (NAFLD), and liver cancer. Recent evidence indicates that autophagy may play a dual role in liver cancer: inhibiting early tumor initiation while promoting progression and malignancy of already formed liver tumors. In this review, we summarized the progress of current understanding of how hepatic viral infection, alcohol consumption and diet-induced fatty liver diseases impair hepatic autophagy. We also discussed how impaired autophagy promotes liver tumorigenesis, and paradoxically how autophagy is required to promote the malignancy and progression of liver cancer. Understanding the molecular mechanisms underlying how autophagy differentially affects liver cancer development and progression may help to design better therapeutic strategies for prevention and treatment of liver cancer.
引用
收藏
页码:606 / 617
页数:12
相关论文
共 134 条
[41]   Persistent activation of Nrf2 through p62 in hepatocellular carcinoma cells [J].
Inami, Yoshihiro ;
Waguri, Satoshi ;
Sakamoto, Ayako ;
Kouno, Tsuguka ;
Nakada, Kazuto ;
Hino, Okio ;
Watanabe, Sumio ;
Ando, Jin ;
Iwadate, Manabu ;
Yamamoto, Masayuki ;
Lee, Myung-Shik ;
Tanaka, Keiji ;
Komatsu, Masaaki .
JOURNAL OF CELL BIOLOGY, 2011, 193 (02) :275-284
[42]   TSC2 mediates cellular energy response to control cell growth and survival [J].
Inoki, K ;
Zhu, TQ ;
Guan, KL .
CELL, 2003, 115 (05) :577-590
[43]   TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling [J].
Inoki, K ;
Li, Y ;
Zhu, TQ ;
Wu, J ;
Guan, KL .
NATURE CELL BIOLOGY, 2002, 4 (09) :648-657
[44]   Crystal Structure of the Ubiquitin-associated (UBA) Domain of p62 and Its Interaction with Ubiquitin [J].
Isogai, Shin ;
Morimoto, Daichi ;
Arita, Kyohei ;
Unzai, Satoru ;
Tenno, Takeshi ;
Hasegawa, Jun ;
Sou, Yu-shin ;
Komatsu, Masaaki ;
Tanaka, Keiji ;
Shirakawa, Masahiro ;
Tochio, Hidehito .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (36) :31864-31874
[45]   p62/SQSTM1 Is a Target Gene for Transcription Factor NRF2 and Creates a Positive Feedback Loop by Inducing Antioxidant Response Element-driven Gene Transcription [J].
Jain, Ashish ;
Lamark, Trond ;
Sjottem, Eva ;
Larsen, Kenneth Bowitz ;
Awuh, Jane Atesoh ;
Overvatn, Aud ;
McMahon, Michael ;
Hayes, John D. ;
Johansen, Terje .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (29) :22576-22591
[46]   Structural basis of p62/SQSTM1 helical filaments and their role in cellular cargo uptake [J].
Jakobi, Arjen J. ;
Huber, Stefan T. ;
Mortensen, Simon A. ;
Schultz, Sebastian W. ;
Palara, Anthimi ;
Kuhm, Tanja ;
Shrestha, Birendra Kumar ;
Lamark, Trond ;
Hagen, Wim J. H. ;
Wilmanns, Matthias ;
Johansen, Terje ;
Brech, Andreas ;
Sachse, Carsten .
NATURE COMMUNICATIONS, 2020, 11 (01)
[47]  
Katsuragi Yoshinori, 2016, Current Opinion in Toxicology, V1, P54, DOI 10.1016/j.cotox.2016.09.005
[48]   p62/SQSTM1 functions as a signaling hub and an autophagy adaptor [J].
Katsuragi, Yoshinori ;
Ichimura, Yoshinobu ;
Komatsu, Masaaki .
FEBS JOURNAL, 2015, 282 (24) :4672-4678
[49]   Akt and mTORC1 Have Different Roles During Liver Tumorigenesis in Mice [J].
Kenerson, Heidi L. ;
Yeh, Matthew M. ;
Kazami, Machiko ;
Jiang, Xiuyun ;
Riehle, Kimberly J. ;
Mcintyre, Rebecca L. ;
Park, James O. ;
Kwon, Steve ;
Campbell, Jean S. ;
Yeung, Raymond S. .
GASTROENTEROLOGY, 2013, 144 (05) :1055-1065
[50]   HMGB1 promotes ductular reaction and tumorigenesis in autophagy-deficient livers (Publication with Expression of Concern. See vol. 129, pg. 2163, 2019) [J].
Khambu, Bilon ;
Huda, Nazmul ;
Chen, Xiaoyun ;
Antoine, Daniel J. ;
Li, Yong ;
Dai, Guoli ;
Koehler, Ulrike A. ;
Zong, Wei-Xing ;
Waguri, Satoshi ;
Werner, Sabine ;
Oury, Tim D. ;
Gong, Zheng ;
Yin, Xiao-Ming .
JOURNAL OF CLINICAL INVESTIGATION, 2018, 128 (06) :2419-2435