Enhanced expression of mRNAs of antisecretory factor-1, gp96, DAD1 and CDC34 in human hepatocellular carcinomas

Biochim Biophys Acta. 2001 Apr 30;1536(1):1-12. doi: 10.1016/s0925-4439(01)00026-6.

Abstract

To identify differentially expressed genes in hepatocarcinogenesis, we performed differential display analysis using surgically resected hepatocellular carcinoma (HCC) and adjacent non-tumorous liver tissues. We identified four cDNA fragments upregulated in HCC samples, encoding antisecretory factor-1 (AF), gp96, DAD1 and CDC34. Northern blot analysis demonstrated that these mRNAs were expressed preferentially in HCCs compared with adjacent non-tumorous liver tissues or normal liver tissues from non-HCC patients. The expression of these mRNAs was increased along with the histological grading of HCC tissues. These mRNA levels were also high in three human HCC cell lines (HuH-7, HepG2 and HLF), irrespective of the growth state. We also demonstrate that sodium butyrate, an inducer of differentiation, downregulated the expression of AF and gp96 mRNAs, supporting in part our pathological observation. Immunohistochemical analysis revealed that gp96 and CDC34 proteins were preferentially accumulated in cytoplasm and nuclei of HCC cells, respectively. Overexpression of these genes could be an important manifestation of HCC phenotypes and should provide clues to understand the molecular basis of hepatocellular carcinogenesis.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Anaphase-Promoting Complex-Cyclosome
  • Antigens, Neoplasm / genetics*
  • Antigens, Neoplasm / metabolism
  • Apoptosis Regulatory Proteins
  • Blotting, Northern
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / pathology
  • DNA, Complementary / isolation & purification
  • Disease Progression
  • Female
  • Genetic Markers
  • Humans
  • Immunohistochemistry
  • Ligases / genetics*
  • Ligases / metabolism
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / pathology
  • Male
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Middle Aged
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism*
  • Tumor Cells, Cultured
  • Ubiquitin-Conjugating Enzymes
  • Ubiquitin-Protein Ligase Complexes*
  • Ubiquitin-Protein Ligases
  • Up-Regulation

Substances

  • Antigens, Neoplasm
  • Apoptosis Regulatory Proteins
  • DAD1 protein, human
  • DNA, Complementary
  • Genetic Markers
  • Membrane Proteins
  • RNA, Messenger
  • sarcoma glycoprotein gp96 rejection antigens
  • CDC34 protein, human
  • Ubiquitin-Conjugating Enzymes
  • Ubiquitin-Protein Ligase Complexes
  • Anaphase-Promoting Complex-Cyclosome
  • Ubiquitin-Protein Ligases
  • Ligases