Molecular signature in three types of hepatocellular carcinoma with different viral origin by oligonucleotide microarray

Int J Oncol. 2004 Mar;24(3):565-74.

Abstract

Chronic infection with hepatitis B or C virus (HBV or HCV) is the most clearly established risk factor for hepato-cellular carcinoma (HCC). One type of HCC (non-B, non-C HCC) also appears to develop in patients negative for both HBV and HCV. Using a supervised learning method, we investigated gene expression in 11 non-B, non-C HCCs with high-density oligonucleotide microarrays, and compared the patterns of gene expression with those of HBV-infected HCCs (B-type HCCs) and HCV-infected HCCs (C-type HCCs) in the previous dataset. Our gene selection identified 112 and 64 genes that were differentially expressed in non-B, non-C HCC in comparison with B- and C-type HCCs, respectively. In both gene selections, we found that the false discovery rate, the percentage of genes identified by chance, was less than 5%. Additionally, in combination with the previous data, our present data revealed a set of genes specific to each type of B- and C-type HCCs and non-B, non-C HCC. Among these, an interferon-induced gene, IFI27, was differentially expressed among all three types of HCCs, and this result was confirmed by RT-PCR. Thus, our present study provides a framework to characterize the molecular features in the three subtypes of HCC with different viral origin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / virology*
  • Codon
  • DNA, Complementary / metabolism
  • Down-Regulation
  • Female
  • Gene Expression Regulation, Neoplastic
  • Hepacivirus / genetics
  • Hepatitis B virus / genetics
  • Humans
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / virology*
  • Male
  • Oligonucleotide Array Sequence Analysis*
  • Oligonucleotides / genetics*
  • Oligonucleotides / metabolism
  • RNA / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Up-Regulation

Substances

  • Codon
  • DNA, Complementary
  • Oligonucleotides
  • RNA