Aberrant methylation and downregulation of sall3 in human hepatocellular carcinoma

AIM: To investigated whether sall3 transcription was regulated by promoter CpG island hypermethylation in hepatocellular carcinoma (HCC). METHODS: The cell lines Huh7, HepG2, SK-HEP1, SMMC7721, Be17402, QGY7703 and a cohort of 38 HCC tissue specimens and corresponding nontumorous tissues were subjected to analysis for sall3 promoter CpG island methylation and mRNA transcription. sall3 promoter CpG island nnethylation levels were determined using the MassARRAY platform and mRNA transcription levels of the gene were detected by quantitative real-time polymerase chain reaction. RESULTS: The levels of sall3 mRNA were decreased by more than twofold in 33 of 38 tumor tissues compared to adjacent noncancerous tissues. Among these 33 tumor tissues with lower levels of sall3 mRNA, 24 showed higher levels of methylation. Based on these results, we hypothesized that the decrease in sall3 mRNA transcription level was likely due to promoter CpG island hypermethylation. Changes in sall3 mRNA transcription and promoter CpG island methylation were determined in the above six cell lines after treatment with 0, 0.1, 0.5 and 2.5 mu mol 5-aza-2-deoxycytidine, a demethylating agent. Promoter CpG island rnethylation levels decreased in a dose-dependent manner in all six cell lines, while the mRNA transcription level increased dosedependently in Huh7, HepG2, SK-HEP1 and SMMC7721 cells and irregularly in Be17402 and QGY7703 cells. CONCLUSION: These results indicated that promoter CpG island hypermethylation contributes to the down-regulation of sall3 mRNA transcription in HCC. (C) 2012 Baishideng. All rights reserved.