Coexpression of MAGE-A peptides and HLA class I molecules in hepatocellular carcinoma

Anticancer Res. 2010 May;30(5):1617-23.

Abstract

Melanoma antigen (MAGE)-A derived peptides are tumour-specific and induce a strong in vitro T-cell response, if presented with human leukocyte antigen (HLA) molecules, which are involved in T-cell-mediated immune surveillance. MAGE-A-derived peptides are recognised by autologous cytotoxic T lymphocytes. The MAGE-A expression profile of hepatocellular carcinomas (HCC) was analysed by PCR assay covering MAGE-A transcripts in 13 patients. MAGE-A peptide expression was determined using a reverse transcription-PCR method. Cryostat sections were stained with monoclonal antibodies directed against HLA class I molecules. Twelve (92.3%) out of thirteen tumours expressed one MAGE-A gene. In at least 90% of the tumours, one MAGE-A peptide was expressed. Determination of the HLA status of the tumours showed a significant loss in approximately 40% of the tumours. The tumour-specific expression of MAGE genes and antigens encoded by a MAGE-family gene may represent useful targets for tumour-specific immunotherapy in HCC patients, in addition to established treatment options.

MeSH terms

  • Aged
  • Antibodies, Monoclonal / chemistry
  • Antigens, Neoplasm / biosynthesis*
  • Antigens, Neoplasm / metabolism
  • Carcinoma, Hepatocellular / metabolism*
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Histocompatibility Antigens Class I / biosynthesis*
  • Humans
  • Immunotherapy / methods
  • Liver Neoplasms / metabolism*
  • Male
  • Melanoma-Specific Antigens
  • Middle Aged
  • Models, Biological
  • Neoplasm Proteins / biosynthesis*
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Antibodies, Monoclonal
  • Antigens, Neoplasm
  • Histocompatibility Antigens Class I
  • Melanoma-Specific Antigens
  • Neoplasm Proteins