Silencing of Hint1, a novel tumor suppressor gene, by promoter hypermethylation in hepatocellular carcinoma
Journal
Cancer Letters
Journal Volume
275
Journal Issue
2
Pages
277-284
Date Issued
2009
Author(s)
Abstract
The Hint1 protein, a member of the histidine triad (HIT) family, is highly conserved in diverse species and ubiquitously expressed in mammalian tissues. Previous studies in mice provided evidence that Hint1 may be haploinsufficient with respect to its function as a tumor suppressor. In the present study, we investigated the aberrant methylation of Hint1 and explored possible relationships between aberrant methylation and clinicopathological features in hepatocellular carcinoma (HCC). Hypermethylation of Hint1 was evaluated by the methylation specific PCR (MSP) method in 40 patients with HCC (tumor and paired adjacent non-tumor tissues) from Taiwan, 22 cases of normal liver tissue (14 from Taiwan and 8 from the US). HINT1 expression in tissues was detected by immunohistochemistry. The frequencies of hypermethylation of Hint1 in tumor, paired adjacent non-tumor and normal liver tissue were 55.0%, 37.5% and 9.1%, respectively. A statistically significant inverse association was found between Hint1 methylation status and expression of the HINT1 protein in tumor tissues (p = 0.003). The relationship between Hint1 methylation status and clinical features and other, previously measured biomarkers was also analyzed. p16 hypermethylation was statistically significantly associated with Hint1 methylation status (p = 0.035). There were no correlations between Hint1 methylation and hepatitis B (HBV) or hepatitis C (HCV) infection status or aflatoxin B1 (AFB1-) and polycyclic aromatic hydrocarbons (PAHs)-DNA adduct levels. These results suggest that promoter hypermethylation of Hint1 may play a role in hepatocarcinogenesis. ? 2008 Elsevier Ireland Ltd. All rights reserved.
SDGs
Other Subjects
aflatoxin B1; polycyclic aromatic hydrocarbon; protein p16; adult; aged; article; clinical article; clinical feature; controlled study; female; gene expression; gene silencing; hepatitis B; hepatitis C; hint1 gene; histopathology; human; human tissue; immunohistochemistry; liver cell carcinoma; male; methylation; polymerase chain reaction; priority journal; Taiwan; tumor suppressor gene; Adult; Aged; Base Sequence; Carcinoma, Hepatocellular; DNA Methylation; DNA Primers; Female; Gene Silencing; Humans; Immunohistochemistry; Liver Neoplasms; Male; Middle Aged; Nerve Tissue Proteins; Polymerase Chain Reaction; Promoter Regions, Genetic; Hepatitis C virus; Mammalia; Mus
Type
journal article