Expression of <i>MAGE</i> genes in primary and metastatic cutaneous melanoma

Francis Brasseur(Ludwig Cancer Research), Donata Rimoldi(Ludwig Cancer Research), Danielle Líénard(University Hospital of Lausanne), Bernard Lethé(Ludwig Cancer Research), S Carrel(Ludwig Cancer Research), Flavio Arienti(Fondazione IRCCS Istituto Nazionale dei Tumori), Ludwig Suter(Fachklinik Hornheide), R Vanwijck(UCLouvain), André Bourlond(UCLouvain), Yves Humblet(Cliniques Universitaires Saint-Luc), Angelo Vacca(University of Bari Aldo Moro), Marina Conese(University of Bari Aldo Moro), Thierry Lahaye(University of Liège), Gérard Degiovanni(University of Liège), Rika Deraemaecker(Université Libre de Bruxelles), M. Beauduin(Hôpital de Jolimont), Xavier Sastre(Institut Curie), E. Salamon(Clinique Saint-Joseph), Brigitte Dréno(Centre Hospitalier Universitaire de Nantes), Elke Jäger(Goethe University Frankfurt), A. Knuth(Goethe University Frankfurt), Christine Chevreau(Institut Claudius Regaud), Stefan Suciu(European Organisation for Research and Treatment of Cancer), Jean‐Marie Lachapelle(UCLouvain), P Pouillart(Institut Curie), Giorgio Parmiani(Fondazione IRCCS Istituto Nazionale dei Tumori), Ferdy J. Lejeune(University Hospital of Lausanne), Jean‐Charles Cerottini(Ludwig Cancer Research), Thierry Boon(Ludwig Cancer Research), Marie Marchand(Ludwig Cancer Research)
International Journal of Cancer
November 3, 1995
Cited by 285

Abstract

Human genes MAGE-1 and MAGE-3 code for antigens that are recognized on melanoma cells by autologous cytolytic T lymphocytes. These antigens may constitute useful targets for specific anti-tumor immunization of cancer patients, since genes MAGE-1 and MAGE-3 are expressed in a number of tumors of different histological types, but are not expressed in normal adult tissues other than testis. This also applies to genes MAGE-2 and MAGE-4, which are closely related to MAGE-1 and MAGE-3. We have analyzed the expression of these 4 MAGE genes in cutaneous melanoma. Sixteen of 100 primary tumors vs. 69 (48%) of 145 metastases from individual patients expressed MAGE-1. Similar differences in the frequency of gene expression between primary and metastatic tumor samples were observed for MAGE-2, MAGE-3, and MAGE-4. MAGE expression in primary tumors was correlated with tumor thickness: there was a significantly increased frequency in the expression of MAGE-1, -2 and -3 in tumors of greater thickness. Benign and dysplastic nevi, as well as in situ melanomas, did not express any of the 4 MAGE genes.


Related Papers

No related papers found

Powered by citation graph analysis