Differential DNA Methylation Associated with Hepatitis B Virus Infection in Hepatocellular Carcinoma
Resource
INTERNATIONAL JOURNAL OF CANCER v.121 n.6 pp.1257-1264
Journal
INTERNATIONAL JOURNAL OF CANCER
Journal Volume
v.121
Journal Issue
n.6
Pages
1257-1264
Date Issued
2007
Date
2007
Author(s)
LEE, TE-CHANG
LEE, PO-HUANG
JENG, YUNG-MING
Abstract
Gene inactivation through DNA hypermethylation plays a pivotal role in carcinogenesis. This study aimed to profile aberrant DNA methylation in different stages of liver disease, namely noncirrhosis, cirrhosis and hepatocellular carcinoma (HCC), and also to clarify the influence of hepatitis B virus (HBV) infection on the aberrant DNA methylation in HCCs. Promoter methylation in p14(ARF), P16( INK4a), O-6-methylguanine-DNA methyltransferase (MGMT), glutathione S-transferase pi (GSTP1) and E- cadherin (E-Cad) genes of 58 HCCs paired with adjacent nontumorous tissues was assayed by methylation-specific PCR. HBV infection was determined using a hepatitis B virus surface antigen (HBsAg) serological assay. The frequency of p16(INK4a) promoter methylation increased from noneirrhotic, cirrhotic, to HCC tissues (noncirrhotic vs. HCC, p < 0.001), while that of GSTP1 promoter methylation increased in cirrhotic tissues compared to noncirrbotic ones (p = 0.029). The frequency of GSTP1 promoter hypermethylation is significantly higher in HCC than in nonturnorous tissues (P = 0.022) from HBsAg- positive patients, but not the HBsAg- negative controls (p = 0.289). While the frequency of E-Cad promoter hypermethylation remained high in both nontumorous tissues and HCCs from HBsAg-positive patients (p = 0.438), it was lower in HCCs than in nontumorous tissues from HBsAg-netive patients (p = 0.002). In contrast, the frequency of p16(INK4 a),MGMT and p14(ARF) promoter hypermethylation in HCCs was unrelated to HBsAg status. In conclusion, aberrant DNA methylation may begin at different stages of liver disease in a gene- dependent manner. Moreover, HBV infection may enhance or maintain GSTP1 and E-Cad promoter methylation and thereby affect hepatocarcinogenesis. (c ) 2007 Wiley-Liss, Inc.
Subjects
hepatitis virus
hepatocellular carcinoma
hyper-methylation
methylation-specific polymerase chain reaction
p14(ARF)
p16(INK4a)
O-6-methylguanine-DNA methyltransferase
SDGs
Type
journal article