Expression of MAGE-A cancer/testis antigens in esophageal squamous cell carcinomas

Anticancer Res. 2006 May-Jun;26(3B):2281-7.

Abstract

Background: Although the diagnosis and therapy of esophageal cancer have improved over the past decade, the prognosis remains dismal. Since MAGE-A cancer/testis antigens (CTA) are potential targets for immunotherapy, this study was aimed at evaluating their expression in these patients and its prognostic value.

Materials and methods: Using 57B monoclonal antibody, MAGE-A CTA expression was analyzed in paraffin-embedded tumor specimens of 98 patients with esophageal squamous cell carcinoma or adenocarcinomas who had undergone surgical resection. For all patients, a postoperative follow-up of at least 4 years was available. The expression was quantified using a scoring system considering intensity and homogeneity of the immunostaining. The prognostic relevance of MAGE-A expression was analyzed in univariate analyses as well as Cox proportional hazard regression analysis.

Results: 57B positivity could be detected in 38 tumors (38.8%). Positive staining was observed in five out of 32 adenocarcinomas (15.2%) and in 33 out of 66 (50%) squamous cell carcinomas. MAGE-A expression did not correlate with the TNM classification, grading or age of the patients. Both univariate (p=0.88) and multivariate analyses (p = 0.82) revealed that MAGE-A expression lacked prognostic significance in esophageal carcinomas.

Conclusion: MAGE-A was expressed in half of the squamous cell carcinomas of the esophagus, but rarely in adenocarcinomas. Although its immunodetection was insufficient for prognostic evaluation, the high expression rate suggests MAGE-A as a potential target for immunotherapy in the first group with the ability for pretherapeutic testing.

MeSH terms

  • Adult
  • Aged
  • Antigens, Neoplasm / biosynthesis*
  • Esophageal Neoplasms / immunology*
  • Esophageal Neoplasms / pathology
  • Female
  • Humans
  • Male
  • Melanoma-Specific Antigens
  • Membrane Proteins / biosynthesis
  • Middle Aged
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Staging
  • Neoplasms, Squamous Cell / immunology*
  • Neoplasms, Squamous Cell / pathology
  • Proportional Hazards Models

Substances

  • Antigens, Neoplasm
  • CTAG1B protein, human
  • MAGEA1 protein, human
  • Melanoma-Specific Antigens
  • Membrane Proteins
  • Neoplasm Proteins