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Updated: Feb 13, 2026

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Published on: June 18, 2020
Correlation between hepatic human males absent on the first (hMOF) and viral persistence in chronic hepatitis B
Liwen Chen1, Chuanwu Zhu2, Fengdi Li1
11Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025 China.
Insights
Human males absent on the first (hMOF), a histone acetyltransferase, correlates with Hepatitis B virus (HBV) DNA replication in chronic hepatitis B (CHB) patients. This suggests hMOF may play a role in HBV clearance and pathogenesis.
Area of Science:
- Hepatology
- Virology
- Molecular Biology
Background:
- Chronic hepatitis B (CHB) is a significant global health issue.
- Hepatocellular carcinoma (HCC) is a major complication of CHB.
- The role of human males absent on the first (hMOF) in HBV replication is not fully understood.
Purpose of the Study:
- To investigate the correlation between hepatic hMOF and HBV DNA replication in CHB patients.
- To explore the potential role of hMOF in CHB pathogenesis and HBV clearance.
Main Methods:
- Liver biopsy samples from CHB patients (HBeAg+ and HBeAg-) and healthy controls were analyzed.
- Immunohistochemistry, qPCR, and Western blot were used to determine hMOF levels.
- Correlation analysis was performed between hMOF, HBV DNA, HBsAg, and HBeAg.
Main Results:
- A positive correlation was found between hepatic hMOF and HBV DNA in all CHB patients.
- hMOF showed a positive correlation with HBsAg and/or HBeAg in HBeAg+ CHB patients.
- No correlation was observed between hMOF and hepatic inflammation or fibrosis.
Conclusions:
- Hepatic hMOF may contribute to the host's ability to clear HBV.
- hMOF might be involved in the pathogenesis of CHB.
- Further research into hMOF's role could offer new therapeutic strategies for CHB.
Background:
Chronic hepatitis B (CHB) remains a global health dilemma with high morbidity and mortality. Human males absent on the first (hMOF) (a histone acetyltransferase) is responsible for DNA damage repair, tumorigenesis and cell cycle regulation. Persistence of HBV DNA contributes to cirrhosis and hepatocellular carcinoma (HCC) in CHB patients. Histone acetyltransferase enhances HBV replication, however the precise underlying mechanism of hMOF in HBV replication in CHB patients remains to be explored. This study aims to investigate the correlation between hepatic hMOF and HBV DNA replication in CHB patients, and may provide new insights towards the treatment of CHB patients.
Methods:
hMOF in liver biopsy (CHB, n = 33 HBeAg+; n = 20 HBeAg-, and three healthy controls) was determined, using immunohistochemistry, qPCR and Western blot. The correlation between hMOF and HBsAg, as well as, HBeAg were determined.
Results:
A positive correlation between hMOF and HBV DNA in overall CHB patients was observed. A distinct positive correlation between hMOF and HBsAg and/or HBeAg in HBeAg+ CHB patients was also detected, however not observed between hMOF and HBsAg in HBeAg- CHB patients. No correlation was observed between hMOF and hepatic inflammation severity and fibrotic stage in CHB patients.
Conclusions:
Hepatic hMOF might contribute to host HBV clearance in CHB patients and possible pathogenesis.
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