A Pleiotropic Role of the Hepatitis B Virus Core Protein in Hepatocarcinogenesis

• Published in: International journal of molecular sciences 2021-12, Vol.22 (24), p.13651
• Main Authors: Lefeuvre, Caroline, Le Guillou-Guillemette, Hélène, Ducancelle, Alexandra
• Format: Article
• Language: English
• Subjects: Antigens; Apoptosis; Carcinogenesis; Carcinogens; Carcinoma, Hepatocellular - genetics; Carcinoma, Hepatocellular - virology; Cell cycle; Cell Movement; Cell Proliferation; Chronic infection; Core protein; Cytokines; DNA methylation; Epigenetics; Gene expression; Gene Expression Regulation, Neoplastic; Gene Regulatory Networks; Genomes; Hepatitis B; Hepatitis B virus - metabolism; Hepatitis B virus - pathogenicity; Hepatitis B, Chronic - complications; Hepatitis B, Chronic - genetics; Hepatocellular carcinoma; Hepatocytes; Hepatoma; Humans; Immune system; Infections; Inflammation; Kinases; Life Sciences; Liver; Liver cancer; Liver Neoplasms - genetics; Liver Neoplasms - virology; Localization; Metabolic pathways; Metastases; Nucleocapsids; Phosphorylation; Promoter Regions, Genetic; Proteins; Review; Sarcoma; Signal transduction; Viral Core Proteins - metabolism; Virus Replication; Viruses
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms222413651

Chronic hepatitis B virus (HBV) infection is one of the most common factors associated with hepatocellular carcinoma (HCC), which is the sixth most prevalent cancer among all cancers worldwide. However, the pathogenesis of HBV-mediated hepatocarcinogenesis is unclear. Evidence currently available suggests that the HBV core protein (HBc) plays a potential role in the development of HCC, such as the HBV X protein. The core protein, which is the structural component of the viral nucleocapsid, contributes to almost every stage of the HBV life cycle and occupies diverse roles in HBV replication and pathogenesis. Recent studies have shown that HBc was able to disrupt various pathways involved in liver carcinogenesis: the signaling pathways implicated in migration and proliferation of hepatoma cells, apoptosis pathways, and cell metabolic pathways inducing the development of HCC; and the immune system, through the expression and production of proinflammatory cytokines. In addition, HBc can modulate normal functions of hepatocytes through disrupting human host gene expression by binding to promoter regions. This HBV protein also promotes HCC metastasis through epigenetic alterations, such as micro-RNA. This review focuses on the molecular pathogenesis of the HBc protein in HBV-induced HCC.