Mulcahy K A, Rimoldi D, Brasseur F, Rodgers S, Liénard D, Marchand M, Rennie I G, Murray A K, McIntyre C A, Platts K E, Leyvraz S, Boon T, Rees R C
Institute for Cancer Studies, University of Sheffield, Sheffield, UK.
Int J Cancer. 1996 Jun 11;66(6):738-42. doi: 10.1002/(SICI)1097-0215(19960611)66:6<738::AID-IJC5>3.0.CO;2-0.
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.
此前有报道称,MAGE-1、-2、-3和-4基因在包括皮肤黑色素瘤在内的人类癌症中表达。MAGE-1和MAGE-3是特异性免疫疗法的靶点,因为它们编码的肽抗原在由HLA I类分子呈递时可被细胞毒性T淋巴细胞(CTL)识别,目前针对这些肽的临床试验正在进行中。MAGE基因家族的其他成员也可能编码被CTL识别的抗原。葡萄膜黑色素瘤与皮肤黑色素瘤一样,起源于神经嵴衍生的黑素细胞。为了确定葡萄膜黑色素瘤患者是否适合MAGE肽免疫疗法,通过逆转录后进行聚合酶链反应(RT-PCR)扩增和溴化乙锭染色来评估MAGE-1、-2、-3和-4基因的表达。在27个原发性肿瘤中均未检测到MAGE基因的表达。在26个转移样本中,只有2个样本表达了MAGE-1或MAGE-4,但未检测到MAGE-2或-3的表达。我们的数据表明,与皮肤黑色素瘤不同,葡萄膜黑色素瘤可能不是MAGE肽免疫疗法的合适候选对象。