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. 2003 Sep;163(3):1101-7.
doi: 10.1016/S0002-9440(10)63469-4.

Aberrant promoter methylation profiles of tumor suppressor genes in hepatocellular carcinoma

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Aberrant promoter methylation profiles of tumor suppressor genes in hepatocellular carcinoma

Bin Yang et al. Am J Pathol. 2003 Sep.

Abstract

Hepatocellular carcinoma (HCC) is one of the most fatal human malignancies, but the molecular mechanisms of hepatocarcinogenesis remain unclear. Although p53 mutations are frequently observed in Asian HCC, it is not a common event in Western HCC. Recent studies suggest that tumor suppressor genes (TSGs) can also be silenced through epigenetic disruption, such as promoter CpG island methylation, during carcinogenesis. To further understand the molecular mechanism of hepatocarcinogenesis, we have investigated the promoter methylation status of nine TSGs (SOCS-1, GSTP, APC, E-cadherin, RAR-beta, p14, p15, p16, and p73) in 51 cases of HCC using methylation-specific polymerase chain reaction. We found that 82% of HCCs had methylation of at least one TSG promoter. The most frequently methylated TSGs in HCC were: SOCS-1 (65%), GSTP (54%), APC (53%), E-cadherin (49%), and p15 (49%). Methylation of SOCS-1, GSTP, APC, E-cadherin, and p15 was more frequent in HCC than in nontumor liver (P < 0.05). Methylation of SOCS-1, GSTP, and p15 was also significantly more frequent in HCC than cirrhotic liver (P < 0.05). Although methylation of one or two genes could be seen in both nontumor and cirrhotic livers, 53% of the HCC cases had three or more TSG promoters methylated, in comparison to 0% in nontumor liver and 13% in cirrhosis (P = 0.001). Methylation of SOCS-1, APC, and p15 was more frequently seen in hepatitis C virus-positive HCC than hepatitis C virus/hepatitis B virus-negative HCC. Our data suggest that promoter hypermethylation of TSGs is a common event in HCC and may play an important role in hepatocarcinogenesis.

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Figures

Figure 1.
Figure 1.
Methylation profiles of nine TSGs in HCC, cirrhosis, and nontumor livers. Cases were labeled as N1 to N14 for nontumor liver; C1 to C15 for cirrhosis; and HC1 to HC51 for HCC. A filled box indicates that promoter methylation was detected by MSP; an open box indicates that no methylation was detected; × indicates a noninformative specimen.
Figure 2.
Figure 2.
Association of TSG promoter methylation with the viral status of HCC. The percentage of HCC cases with TSG methylation is indicated for groups of patients that are positive for HBV, HCV, and neither HBV nor HCV.

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