Comprehensive DNA methylation analysis of hepatitis B virus genome in infected liver tissues

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Surbhi Jain
Ting-Tsung Chang
Sitong Chen
Batbold Boldbaatar
Adam Clemens
Selena Y. Lin
Ran Yan
Chi-Tan Hu
Haitao Guo
Timothy M. Block
Wei Song
Ying-Hsiu Su
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[1] JBS Science,Department of Internal Medicine
[2] Inc.,Department of Microbiology and Immunology
[3] National Cheng Kung University Medical College and Hospital,Department of Medicine
[4] Drexel University College of Medicine,undefined
[5] Buddhist Tzu Chi General Hospital and Tzu Chi University,undefined
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Hepatitis B virus (HBV) is a hepatotropic virus causing hepatitis, cirrhosis and hepatocellular carcinoma (HCC). The methylation status of the HBV DNA in its different forms can potentially provide insight into the pathogenesis of HBV-related liver diseases, including HCC, however this is unclear. The goal of this study is to obtain comprehensive DNA methylation profiles of the three putative CpG islands in the HBV DNA in infected livers, with respect to liver disease progression. The extent of methylation in these CpG islands was first assessed using bisulfite PCR sequencing with a small set of tissue samples, followed by analysis using both quantitative bisulfite-specific PCR and quantitative methylation-specific PCR assays in a larger sample size (n = 116). The level of HBV CpG island 3 methylation significantly correlated with hepatocarcinogenesis. We also obtained, for the first time, evidence of rare, non-CpG methylation in CpG island 2 of the HBV genome in infected liver. Comparing methylation of the HBV genome to three known HCC-associated host genes, APC, GSTP1 and RASSF1A, we did not identify a significant correlation between these two groups.
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