Decreased PADI4 mRNA association with global hypomethylation in hepatocellular carcinoma during HBV exposure

Cell Biochem Biophys. 2013 Mar;65(2):187-95. doi: 10.1007/s12013-012-9417-3.

Abstract

To gain insight into the role of peptidylarginine deiminase type 4 (PADI4), we determined the relationship between PADI4 mRNA and global hypomethylation during HBV exposure in hepatocarcinogenesis. We analyzed Line-1 methylation by MSP, and CD133 mRNA by real-time PCR in 74 HCC. The HCC cancer lines (7721, Huh7, and Hep-G2) were treated with 5-Aza-CdR and TSA. PADI4 mRNA were lower in HCC tissues (Mean(-∆Ct) = 1.41) than that in Non-Hcc tissues (Mean(-∆Ct) = 3.10). Expression of PADI4 was elevated in only 20 (27 %) of the 74 HCC patients but decreased in 54 (73 %) of the patients. The declined PADI4 mRNA was significantly associated with Line-1 demethylation in HCC patients. PADI4 mRNA were lower in HCC patients with Line-1 ∆MI <-0.15 (Mean(-∆∆Ct) = -2.66) than those with Line-1 ∆MI >= -0.15 (Mean(-∆∆Ct) = -1.02). The results suggested that HCC showing hypomethylation of Line-1 is considered to be silencing PADI4 mRNA. And the lower PADI4 mRNA was also found in HCC patients with HBV >= 10(5) (copy/ml) than those with HBV < 10(5) (copy/ml). After treated by 5-Aza-CdR and TSA, we found that PADI4 mRNA induced significantly by TSA in Huh7 and Hep-G2 cells, but not in 7721 cells. Meanwhile, PADI4 mRNA induced by the combination of 5-Aza-CdR and TSA in HCC cells, and it could no effect for exposure to 5-Aza-CdR alone. The results suggested that decreased PADI4 mRNA is associated with global hypomethylation in HCC during HBV exposure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Azacitidine / analogs & derivatives
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / virology
  • Cell Line, Tumor
  • DNA Methylation*
  • DNA Modification Methylases / antagonists & inhibitors
  • Decitabine
  • Female
  • Gene Expression Regulation, Neoplastic
  • Hep G2 Cells
  • Hepatitis B / virology
  • Hepatitis B virus / physiology
  • Histone Deacetylase Inhibitors / pharmacology
  • Host-Pathogen Interactions
  • Humans
  • Hydrolases / genetics*
  • Hydrolases / metabolism
  • Hydroxamic Acids / pharmacology
  • Immunohistochemistry
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / pathology
  • Liver Neoplasms / virology
  • Long Interspersed Nucleotide Elements / genetics
  • Male
  • Middle Aged
  • Protein-Arginine Deiminase Type 4
  • Protein-Arginine Deiminases
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Survival Analysis

Substances

  • Histone Deacetylase Inhibitors
  • Hydroxamic Acids
  • RNA, Messenger
  • trichostatin A
  • Decitabine
  • DNA Modification Methylases
  • Hydrolases
  • PADI4 protein, human
  • Protein-Arginine Deiminase Type 4
  • Protein-Arginine Deiminases
  • Azacitidine