Effect of 5-aza-2'-deoxycytidine on immune-associated proteins in exosomes from hepatoma

World J Gastroenterol. 2010 May 21;16(19):2371-7. doi: 10.3748/wjg.v16.i19.2371.

Abstract

Aim: To study the effect of 5-aza-2'-deoxycytidine (5-aza-CdR) on heat shock protein 70 (HSP70), human leucocyte antigen-I (HLA-I) and NY-ESO-1 proteins in exosomes produced by hepatoma cells, HepG2 and Hep3B.

Methods: Exosomes derived from HepG(2) and Hep3B cells treated with or without 5-aza-CdR were isolated and purified by ultrafiltration centrifugation and sucrose gradient ultracentrifugation. The number of exosomes was counted under electron microscope. Concentration of proteins in exosomes was measured by bicinchoninic acid protein assay. Expression of HSP70, HLA-I and NY-ESO-1 proteins in exosomes was detected by Western blotting and immunoelectron microscopy. mRNA expression of p53 gene was detected by reverse transcription polymerase chain reaction.

Results: The mRNA expression of p53 gene was increased in both hepatoma cell lines after treatment with 5-aza-CdR. The number of exosomes and the concentration of total proteins in exosomes were increased significantly after treatment with 5-aza-CdR (P < 0.05). After treatment with 5-aza-CdR, immunoelectron microscopy and Western blotting showed that the HSP70, HLA-I and NY-ESO-1 proteins were increased in exosomes produced by both hepatoma cell lines.

Conclusion: 5-Aza-CdR, an inhibitor of DNA methyltransferase, can increase exosomes produced by hepatoma cells and immune-associated protein component of exosomes, which may be mediated by p53 gene up-regulation and 5-aza-CdR demethylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Neoplasm / metabolism
  • Azacitidine / analogs & derivatives*
  • Azacitidine / pharmacology
  • Blotting, Western
  • Carcinoma, Hepatocellular / enzymology
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / immunology*
  • Centrifugation, Density Gradient
  • DNA Modification Methylases / antagonists & inhibitors*
  • DNA Modification Methylases / metabolism
  • Decitabine
  • Enzyme Inhibitors / pharmacology*
  • Exosomes / drug effects*
  • Exosomes / enzymology
  • Exosomes / immunology
  • HLA Antigens / metabolism
  • HSP70 Heat-Shock Proteins / metabolism
  • Hep G2 Cells
  • Humans
  • Liver Neoplasms / enzymology
  • Liver Neoplasms / genetics
  • Liver Neoplasms / immunology*
  • Membrane Proteins / metabolism
  • Microscopy, Immunoelectron
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Suppressor Protein p53 / genetics
  • Up-Regulation

Substances

  • Antigens, Neoplasm
  • CTAG1B protein, human
  • Enzyme Inhibitors
  • HLA Antigens
  • HSP70 Heat-Shock Proteins
  • Membrane Proteins
  • RNA, Messenger
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • Decitabine
  • DNA Modification Methylases
  • Azacitidine