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Title 

Aberrant epigenetic modifications in hepatocarcinogenesis induced by hepatitis B virus X protein

Authors 

In Young ParkBo Hwa SohnE YuD J SuhY H ChungJ H LeeS J SurzyckiYoung Ik Lee

Publisher 

Elsevier

Issue Date 

2007

Citation 

Gastroenterology, vol. 132, no. 4, pp. 1476-1494

Keywords 

bisulfiteDNA methyltransferase 3Bhepatitis B virus X proteinsomatomedin binding protein 3DNA modificationdnmt3b genedot hybridizationepigeneticsexpression vectorhepatitis B virus

Abstract 

Background & Aims: The involvement of the hepatitis B virus X (HBx) protein in epigenetic modifications during hepatocarcinogenesis has not been previously characterized. The aim of the present study was to identify the involvement of HBx in regional hypermethylation and global hypomethylation during the formation of hepatocellular carcinoma (HCC). Methods: Liver cell lines were transiently or stably transfected with an HBx-expressing vector. DNA methyltransferase (DNMT) promoter activity changes were examined by luciferase assay and chromatin immunoprecipitation. The methylation status of insulin-like growth factor binding protein-3 was examined by methyl-specific polymerase chain reaction and bisulfite sequencing. Global DNA methylation levels were examined using 5-methylcytosine dot blot and methylation-sensitive Southern blot analysis. HBx-mediated DNA methylation abnormalities were confirmed in patient HCC samples using methyl-specific polymerase chain reaction and 5-methylcytosine dot blot analysis. Results: HBx expression increased total DNMT activities by up-regulation of DNMT1, DNMT3A1, and DNMT3A2 and selectively promoted regional hypermethylation of specific tumor suppressor genes. HBx specifically repressed insulin-like growth factor-3 expression through de novo methylation via DNMT3A1 and DNMT3A2 and by inhibiting SP1 binding via recruiting methyl CpG binding protein 2 to the newly methylated SP1 binding element. HBx also induced global hypomethylation of satellite 2 repeat sequences by down-regulating DNMT3B. The prevalence of these specific methylation abnormalities by HBx was significantly correlated with HBx expression in HBV-infected HCC patients. Conclusions: Targeted deregulation of DNMTs by HBx promotes both specific regional hypermethylation and global hypomethylation. These epigenetic modulations by HBx may suggest a mechanism for epigenetic tumorigenesis during HBV-mediated hepatocarcinogenesis.

ISSN 

0016-5085

Link 

http://dx.doi.org/10.1053/j.gastro.2007.01.034

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2017-04-19


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