Literature DB >> 8647642

Infrequent expression of the MAGE gene family in uveal melanomas.

K A Mulcahy1, D Rimoldi, F Brasseur, S Rodgers, D Liénard, M Marchand, I G Rennie, A K Murray, C A McIntyre, K E Platts, S Leyvraz, T Boon, R C Rees.   

Abstract

It has previously been reported that MAGE-1, -2, -3 and -4 genes are expressed in human cancers including cutaneous melanoma. MAGE-1 and MAGE-3 represent targets for specific immunotherapy because they encode peptide antigens which are recognised by cytotoxic T lymphocytes (CTL) when presented by HLA class I molecules, and pilot clinical trials with these peptides are currently in progress. It is likely that other members of the MAGE gene family may also encode antigens recognised by CTL. Uveal melanomas, like cutaneous melanomas, arise from melanocytes that are derived from the neural crest. To determine if uveal melanoma patients would be suitable for MAGE-peptide immunotherapy, the expression of MAGE-1, -2, -3 and -4 genes was assessed by reverse transcription followed by polymerase chain reaction (RT-PCR) amplification and ethidium bromide staining. Expression of MAGE genes was not detected in any of 27 primary tumours. Either MAGE-1 or MAGE-4 was expressed in only 2 of 26 metastatic samples, but expression of MAGE-2 or -3 was not detected. Our data suggest that, unlike cutaneous melanomas, uveal melanomas may not be suitable candidates for MAGE-peptide immunotherapy.

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Year:  1996        PMID: 8647642     DOI: 10.1002/(SICI)1097-0215(19960611)66:6<738::AID-IJC5>3.0.CO;2-0

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  12 in total

1.  Human antigen-presenting cell/tumour cell hybrids stimulate strong allogeneic responses and present tumour-associated antigens to cytotoxic T cells in vitro.

Authors:  D J Dunnion; A L Cywinski; V C Tucker; A K Murray; A B Rickinson; P Coulie; M J Browning
Journal:  Immunology       Date:  1999-12       Impact factor: 7.397

Review 2.  Cytolytic T lymphocyte responses of cancer patients to tumor-associated antigens.

Authors:  P Romero
Journal:  Springer Semin Immunopathol       Date:  1996

Review 3.  Immune escape mechanisms of intraocular tumors.

Authors:  Jerry Y Niederkorn
Journal:  Prog Retin Eye Res       Date:  2009-06-27       Impact factor: 21.198

4.  Apoptotic cell death in conjunction with CD80 costimulation confers uveal melanoma cells with the ability to induce immune responses.

Authors:  Jennifer Carlring; Munitta Shaif-Muthana; Karen Sisley; Ian G Rennie; Anna K Murray
Journal:  Immunology       Date:  2003-05       Impact factor: 7.397

5.  Expression of MAGE genes in ocular melanoma during progression from primary to metastatic disease.

Authors:  P W Chen; T G Murray; T Uno; M L Salgaller; R Reddy; B R Ksander
Journal:  Clin Exp Metastasis       Date:  1997-09       Impact factor: 5.150

Review 6.  Chemotherapy and Physical Therapeutics Modulate Antigens on Cancer Cells.

Authors:  Wojciech Szlasa; Natalia Janicka; Natalia Sauer; Olga Michel; Bernadetta Nowak; Jolanta Saczko; Julita Kulbacka
Journal:  Front Immunol       Date:  2022-07-06       Impact factor: 8.786

7.  An immunohistochemical study of altered immunomodulatory molecule expression in head and neck squamous cell carcinoma.

Authors:  A R Vora; S Rodgers; A J Parker; R Start; R C Rees; A K Murray
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

8.  MAGE, BAGE and GAGE: tumour antigen expression in benign and malignant ovarian tissue.

Authors:  A M Gillespie; S Rodgers; A P Wilson; J Tidy; R C Rees; R E Coleman; A K Murray
Journal:  Br J Cancer       Date:  1998-09       Impact factor: 7.640

9.  High expression of immunotherapy candidate proteins gp100, MART-1, tyrosinase and TRP-1 in uveal melanoma.

Authors:  T J de Vries; D Trancikova; D J Ruiter; G N van Muijen
Journal:  Br J Cancer       Date:  1998-11       Impact factor: 7.640

10.  Ex vivo staining of metastatic lymph nodes by class I major histocompatibility complex tetramers reveals high numbers of antigen-experienced tumor-specific cytolytic T lymphocytes.

Authors:  P Romero; P R Dunbar; D Valmori; M Pittet; G S Ogg; D Rimoldi; J L Chen; D Liénard; J C Cerottini; V Cerundolo
Journal:  J Exp Med       Date:  1998-11-02       Impact factor: 14.307

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