Infrequent expression of the MAGE gene family in uveal melanomas

被引:0
|
作者
Mulcahy, KA
Rimoldi, D
Brasseur, F
Rodgers, S
Lienard, D
Marchand, M
Rennie, IG
Murray, AK
McIntyre, CA
Platts, KE
Leyvraz, S
Boon, T
Rees, RC
机构
[1] UNIV LAUSANNE,LAUSANNE BRANCH,LUDWIG INST CANC RES,EPALINGES,SWITZERLAND
[2] LUDWIG INST CANC RES,BRUSSELS,BELGIUM
[3] CATHOLIC UNIV LEUVEN,CELLULAR GENET UNIT,BRUSSELS,BELGIUM
[4] UNIV SHEFFIELD,ROYAL HALLAMSHIRE HOSP,DEPT OPHTHALMOL & ORTHOPT,SHEFFIELD,S YORKSHIRE,ENGLAND
[5] CHU VAUDOIS,CTR PLURIDISCIPLINAIRE ONCOL,LAUSANNE,SWITZERLAND
关键词
D O I
10.1002/(SICI)1097-0215(19960611)66:6<738::AID-IJC5>3.0.CO;2-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 MACE 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. (C) 1996 Wiley-Liss, Inc.
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页码:738 / 742
页数:5
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