It has previously been reported that MAGE-1, -2, -3 and -4 genes are e
xpressed in human cancers including cutaneous melanoma. MAGE-1 and MAG
E-3 represent targets for specific immunotherapy because they encode p
eptide antigens which are recognised by cytotoxic T lymphocytes (CTL)
when presented by HLA class I molecules, and pilot clinical trials wit
h these peptides are currently in progress. It is likely that other me
mbers of the MACE gene family may also encode antigens recognised by C
TL. 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 expres
sion of MAGE-1, -2, -3 and -4 genes was assessed by reverse transcript
ion followed by polymerase chain reaction (RT-PCR) amplification and e
thidium bromide staining. Expression of MAGE genes was not detected in
any of 27 primary tumours. Either MAGE-1 or MAGE-4 was expressed in o
nly 2 of 26 metastatic samples, but expression of MAGE-2 or -3 was not
detected. Our data suggest that, unlike cutaneous melanomas, uveal me
lanomas may not be suitable candidates for MAGE-peptide immunotherapy.
(C) 1996 Wiley-Liss, Inc.