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Modeling Hepatitis B Virus Infection in Non-Hepatic 293T-NE-3NRs Cells
Published on: June 5, 2020
The role of hepatitis B virus genome variations in HBV-related HCC: effects on host signaling pathways
Shahrzad Shoraka1,2, Seyed Mahdi Hosseinian3, Ayda Hasibi4
1Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Insights
Hepatitis B virus (HBV) mutations impact hepatocellular carcinoma (HCC) development by altering cell signaling pathways. Understanding these variations is key to developing targeted therapies for this common liver cancer.
Area of Science:
- Hepatology
- Virology
- Molecular Biology
Background:
- Hepatocellular carcinoma (HCC) is a major global health concern, often linked to viral hepatitis infections.
- Hepatitis B virus (HBV) causes over half of virus-related HCC cases, underscoring its critical role in liver cancer pathogenesis.
- HBV-related HCC development is a complex process influenced by host, viral, and environmental factors.
Purpose of the Study:
- To review the role of HBV in HCC progression.
- To focus on how HBV genome variations affect HCC-related signaling pathways.
- To enhance understanding of molecular pathogenesis and identify therapeutic targets for HBV-related HCC.
Main Methods:
- Literature review focusing on HBV genome variations.
- Analysis of studies linking HBV mutations to host cell signaling pathways.
- Synthesis of information on the impact of viral genetic diversity on HCC development.
Main Results:
- HBV genome mutations and proteins can dysregulate cell signaling pathways crucial for HCC development.
- Different HBV mutants exhibit varying pathogenicity, disease progression, and treatment responses.
- Specific HBV variations are associated with altered host signaling, contributing to HCC.
Conclusions:
- Understanding the interplay between HBV genome variations and host signaling pathways is vital for elucidating HCC pathogenesis.
- Identifying commonly dysregulated pathways in HBV-related HCC can lead to novel therapeutic strategies.
- Targeting specific molecular mechanisms driven by HBV mutations may improve HCC treatment outcomes.
Abstract:
Hepatocellular carcinoma (HCC) is a significant global health issue, with a high prevalence in many regions. There are variations in the etiology of HCC in different regions, but most cases are due to long-term infection with viral hepatitis. Hepatitis B virus (HBV) is responsible for more than 50% of virus-related HCC, which highlights the importance of HBV in pathogenesis of the disease. The development and progression of HBV-related HCC is a complex multistep process that can involve host, viral, and environmental factors. Several studies have suggested that some HBV genome mutations as well as HBV proteins can dysregulate cell signaling pathways involved in the development of HCC. Furthermore, it seems that the pathogenicity, progression of liver diseases, response to treatment and also viral replication are different among HBV mutants. Understanding the relationship between HBV genome variations and host signaling pathway alteration will improve our understanding of the molecular pathogenesis of HBV-related HCC. Furthermore, investigating commonly dysregulated pathways in HBV-related HCC is necessary to discover more specific therapeutic targets and develop more effective strategies for HCC treatment. The objective of this review is to address the role of HBV in the HCC progression and primarily focus on the impacts of HBV genome variations on HCC-related signaling pathways.
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