Molecular Mechanisms Driving Progression of Liver Cirrhosis towards Hepatocellular Carcinoma in Chronic Hepatitis B and C Infections: A Review

被引:249
作者
Kanda, Tatsuo [1 ]
Goto, Taichiro [2 ]
Hirotsu, Yosuke [3 ]
Moriyama, Mitsuhiko [1 ]
Omata, Masao [3 ,4 ]
机构
[1] Nihon Univ, Sch Med, Dept Med, Div Gastroenterol & Hepatol,Itabashi Ku, 30-1 Oyaguchi Kamicho, Tokyo 1738610, Japan
[2] Yamanashi Cent Hosp, Lung Canc & Resp Dis Ctr, 1-1-1 Fujimi, Kofu, Yamanashi 4008506, Japan
[3] Yamanashi Cent Hosp, Genome Anal Ctr, Yamanashi 4008506, Japan
[4] Univ Tokyo, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138655, Japan
关键词
cirrhosis; HBV; HCV; hepatocellular carcinoma; VIRUS X-PROTEIN; INSULIN-RECEPTOR SUBSTRATE-1; INHIBITS CELL-PROLIFERATION; ABERRANT DNA METHYLATION; GROWTH-FACTOR-BETA; NATURAL-HISTORY; CORE PROTEIN; PROMOTES PROLIFERATION; UP-REGULATION; DIFFERENTIAL EXPRESSION;
D O I
10.3390/ijms20061358
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
Almost all patients with hepatocellular carcinoma (HCC), a major type of primary liver cancer, also have liver cirrhosis, the severity of which hampers effective treatment for HCC despite recent progress in the efficacy of anticancer drugs for advanced stages of HCC. Here, we review recent knowledge concerning the molecular mechanisms of liver cirrhosis and its progression to HCC from genetic and epigenomic points of view. Because similar to 70% of patients with HCC have hepatitis B virus (HBV) and/or hepatitis C virus (HCV) infection, we focused on HBV- and HCV-associated HCC. The literature suggests that genetic and epigenetic factors, such as microRNAs, play a role in liver cirrhosis and its progression to HCC, and that HBV- and HCV-encoded proteins appear to be involved in hepatocarcinogenesis. Further studies are needed to elucidate the mechanisms, including immune checkpoints and molecular targets of kinase inhibitors, associated with liver cirrhosis and its progression to HCC.
引用
收藏
页数:24
相关论文
共 225 条
[1]   Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3 [J].
Al-Qahtani, Ahmed ;
Khalak, Hanif G. ;
Alkuraya, Fowzan S. ;
Al-hamoudy, Waleed ;
Alswat, Khalid ;
Al Balwi, Mohammed A. ;
Al AbdulKareem, Ibrahim ;
Sanai, Faisal M. ;
Abdo, Ayman A. .
JOURNAL OF MEDICAL GENETICS, 2013, 50 (11) :725-732
[2]   Increased incidence of liver cancer after successful DAA treatment of chronic hepatitis C: Fact or fiction? [J].
Alberti, Alfredo ;
Piovesan, Sara .
LIVER INTERNATIONAL, 2017, 37 (06) :802-808
[3]   Pleiotrophin, a target of miR-384, promotes proliferation, metastasis and lipogenesis in HBV-related hepatocellular carcinoma [J].
Bai, Pei-song ;
Xia, Nan ;
Sun, Hong ;
Kong, Ying .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2017, 21 (11) :3023-3043
[4]   Tumor suppressor micro RNA miR-145 and onco micro RNAs miR-21 and miR-222 expressions are differentially modulated by Hepatitis B virus X protein in malignant hepatocytes [J].
Bandopadhyay, Manikankana ;
Banerjee, Arup ;
Sarkar, Neelakshi ;
Panigrahi, Rajesh ;
Datta, Sibnarayan ;
Pal, Ananya ;
Singh, Shivram Prasad ;
Biswas, Avik ;
Chakrabarti, Shekhar ;
Chakravarty, Runu .
BMC CANCER, 2014, 14
[5]   Hepatitis C Virus Differentially Modulates Activation of Forkhead Transcription Factors and Insulin-Induced Metabolic Gene Expression [J].
Banerjee, Arup ;
Meyer, Keith ;
Mazumdar, Budhaditya ;
Ray, Ratna B. ;
Ray, Ranjit .
JOURNAL OF VIROLOGY, 2010, 84 (12) :5936-5946
[6]   Hepatitis C virus core protein upregulates serine phosphorylation of insulin receptor substrate-1 and impairs the downstream Akt/Protein kinase B signaling pathway for insulin resistance [J].
Banerjee, Sutapa ;
Saito, Kousuke ;
Ait-Goughoulte, Malika ;
Meyer, Keith ;
Ray, Ratna B. ;
Ray, Ranjit .
JOURNAL OF VIROLOGY, 2008, 82 (06) :2606-2612
[7]   Nrf2-p62 autophagy pathway and its response to oxidative stress in hepatocellular carcinoma [J].
Bartolini, Desiree ;
Dallaglio, Katiuscia ;
Torquato, Pierangelo ;
Piroddi, Marta ;
Galli, Francesco .
TRANSLATIONAL RESEARCH, 2018, 193 :54-71
[8]   Liver fibrosis [J].
Bataller, R ;
Brenner, DA .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (02) :209-218
[9]  
BENVEGNU L, 2003, CANCER, V74, P2442, DOI DOI 10.1002/1097-0142(19941101)74:9
[10]   Hepatitis C Virus Activates the mTOR/S6K1 Signaling Pathway in Inhibiting IRS-1 Function for Insulin Resistance [J].
Bose, Sandip K. ;
Shrivastava, Shubham ;
Meyer, Keith ;
Ray, Ratna B. ;
Ray, Ranjit .
JOURNAL OF VIROLOGY, 2012, 86 (11) :6315-6322