Cancer Immunity, Vol. 8, p. 7 (22 April 2008) Submitted: 16 August 2007. Resubmitted: 6 February 2008. Accepted: 7 March 2008.
Sueli M. Oba-Shinjo1, Otavia L. Caballero2, Achim A. Jungbluth2, Sergio Rosemberg3, Lloyd J. Old2, Andrew J. G. Simpson2 and Suely K. N. Marie1
1Department of Neurology, School of Medicine, University of São Paulo, Av Dr Arnaldo, 455, room 4110, São Paulo, Brazil
2Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA
3Department of Pathology, School of Medicine, University of São Paulo, Av Dr Arnaldo, 455, São Paulo, Brazil
Contributed by: LJ Old
Medulloblastoma is the most common childhood malignant tumor of the central nervous system. Treatment of medulloblastoma requires harmful therapy and nevertheless carries a poor prognosis. Due to their presence in various cancers and their limited expression in normal tissues, CT antigens are ideal vaccine targets for tumor immunotherapy. CT antigens, such as MAGE and NY-ESO-1, have been employed in clinical trials in various malignancies but little is known about their presence in medulloblastoma. We analyzed 25 medulloblastomas for the expression of a panel of CT antigens by RT-PCR and immunohistochemistry. Messenger RNA expression in the samples was as follows: GAGE 64%, MAGEA3/6 56%, SYCP1 44%, SLCO6A1 32%, MAGEC1 28%, MAGEC2 28%, MAGEA4 28%, NY-ESO-1 20%, MAGEA1 16%, and TPTE 0%. All cases except one (96%) were positive for mRNA expression of at least one CT gene. However, CT antigen expression was scarce on a protein level. Immunoreaction to monoclonal antibody E978 (NY-ESO-1) was negative in all cases; MA454 (MAGEA1), 57B (MAGEA4), M3H67 (MAGEA3/6), CT10#5 (MAGEC2) and #23 (GAGE) were each positive in 1 case, while the highest incidence of positive immunostaining, albeit heterogeneous, was seen with CT7-33 (MAGEC1) in 3 out of the 25 cases. The absence of correlation between mRNA and protein expression in medulloblastoma has not been observed in other tumors and further studies addressing the biology of CT antigens are necessary to investigate the present discrepant results.
Copyright © 2008 by Suely K. N. Marie