MAGE-A9 mRNA and protein expression in bladder cancer

Int J Cancer. 2007 May 15;120(10):2170-7. doi: 10.1002/ijc.22282.

Abstract

In a previous analysis, we showed that MAGE-As were the most frequently expressed cancer-testis antigens in human bladder tumours. Here, we further characterized by RT-PCR the expression of this family of genes by analyzing specifically MAGE-A3, -A4, -A8 and -A9 mRNAs in 46 bladder tumours and 10 normal urothelia. We found that they were expressed in 30, 33, 56 and 54% of tumours, respectively. Although MAGE-A8 was the most frequent, its expression was low and was also found in most normal urothelia. The other MAGE-A mRNAs were all tumour-specific but MAGE-A9 mRNA was expressed at a higher level and was two times more frequent in superficial than in invasive tumours. To study the expression of the protein, we produced 2 MAGE-A9-specific monoclonal antibodies (mAbs) presenting no cross-reactivity with other MAGE-A proteins. MAb 14A11, was used to analyse the expression of the antigen in testis and tumour samples by immunohistochemistry. In testis, MAGE-A9 expression was restricted to primary spermatocytes. Most bladder tumours that expressed the MAGE-A9 transcript were positive with mAb 14A11. Staining was heterogeneous but half of the tumours showed over 75% positive cells. Finally, we showed that treatment of bladder cancer cells with the methylation inhibitor, 5-aza-2'-deoxycytidine, alone or in combination with the histone deacetylase inhibitors MS-275 and 4-phenylbutyrate could strongly induce the expression of MAGE-A9. These results show that MAGE-A9 is frequently expressed in superficial bladder cancer and could be a relevant target for immunotherapy or chemoimmunotherapy because its expression can be induced by chemotherapeutic drugs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / biosynthesis
  • Antibodies, Monoclonal / immunology
  • Antigens, Neoplasm / biosynthesis*
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology
  • Azacitidine / analogs & derivatives
  • Azacitidine / pharmacology
  • Benzamides / pharmacology
  • Cell Line, Tumor
  • Decitabine
  • Gene Expression
  • Histone Deacetylase Inhibitors
  • Humans
  • Immunohistochemistry
  • Male
  • Neoplasm Proteins / biosynthesis*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / immunology
  • Phenylbutyrates / pharmacology
  • Protein Isoforms
  • Pyridines / pharmacology
  • RNA, Messenger / biosynthesis*
  • RNA, Messenger / genetics
  • Testicular Neoplasms / genetics
  • Testicular Neoplasms / immunology
  • Urinary Bladder Neoplasms / genetics*
  • Urinary Bladder Neoplasms / immunology*

Substances

  • Antibodies, Monoclonal
  • Antigens, Neoplasm
  • Benzamides
  • Histone Deacetylase Inhibitors
  • MAGEA9 protein, human
  • Neoplasm Proteins
  • Phenylbutyrates
  • Protein Isoforms
  • Pyridines
  • RNA, Messenger
  • entinostat
  • Decitabine
  • 4-phenylbutyric acid
  • Azacitidine