PLoS ONE (Jan 2011)

MAGE-C2/CT10 protein expression is an independent predictor of recurrence in prostate cancer.

  • Lotta von Boehmer,
  • Lukas Keller,
  • Ashkan Mortezavi,
  • Maurizio Provenzano,
  • Giovanni Sais,
  • Thomas Hermanns,
  • Tullio Sulser,
  • Achim A Jungbluth,
  • Lloyd J Old,
  • Glen Kristiansen,
  • Maries van den Broek,
  • Holger Moch,
  • Alexander Knuth,
  • Peter J Wild

DOI
https://doi.org/10.1371/journal.pone.0021366
Journal volume & issue
Vol. 6, no. 7
p. e21366

Abstract

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The cancer-testis (CT) family of antigens is expressed in a variety of malignant neoplasms. In most cases, no CT antigen is found in normal tissues, except in testis, making them ideal targets for cancer immunotherapy. A comprehensive analysis of CT antigen expression has not yet been reported in prostate cancer. MAGE-C2/CT-10 is a novel CT antigen. The objective of this study was to analyze extent and prognostic significance of MAGE-C2/CT10 protein expression in prostate cancer. 348 prostate carcinomas from consecutive radical prostatectomies, 29 castration-refractory prostate cancer, 46 metastases, and 45 benign hyperplasias were immunohistochemically analyzed for MAGE-C2/CT10 expression using tissue microarrays. Nuclear MAGE-C2/CT10 expression was identified in only 3.3% primary prostate carcinomas. MAGE-C2/CT10 protein expression was significantly more frequent in metastatic (16.3% positivity) and castration-resistant prostate cancer (17% positivity; p<0.001). Nuclear MAGE-C2/CT10 expression was identified as predictor of biochemical recurrence after radical prostatectomy (p = 0.015), which was independent of preoperative PSA, Gleason score, tumor stage, and surgical margin status in multivariate analysis (p<0.05). MAGE-C2/CT10 expression in prostate cancer correlates with the degree of malignancy and indicates a higher risk for biochemical recurrence after radical prostatectomy. Further, the results suggest MAGE-C2/CT10 as a potential target for adjuvant and palliative immunotherapy in patients with prostate cancer.