Mori M, Inoue H, Mimori K, Shibuta K, Baba K, Nakashima H, Haraguchi M, Tsuji K, Ueo H, Barnard G F, Akiyoshi T
Department of Surgery, Kyushu University, Beppu, Japan.
Ann Surg. 1996 Aug;224(2):183-8. doi: 10.1097/00000658-199608000-00011.
The human genes MAGE-1 and -3 encode tumor-specific peptide antigens, which are recognized by autologous cytotoxic T lymphocytes. The antigens coded by those genes may be useful for cancer immunotherapy. There is, however, little information on the expression of these genes in human colorectal carcinomas.
The expression of MAGE-1, -2, and -3 genes in 54 pairs of tumor and corresponding normal tissue specimens of the colorectum was determined by means of reverse transcription polymerase chain reaction. The induction of MAGE-1, -2, -3, and -4 gene expression in eight colorectal carcinoma cell lines also was examined by use of a demethylating agent, 5-Aza-2'-deoxycytidine (DAC).
The expression of MAGE genes was not recognized in normal colorectal tissues at all. In tumor tissue specimens, the expression of MAGE-1, -2, and -3 was recognized in 16 (30%), 15 (28%), and 11 (20%) patients, respectively. The expression was seen frequently in patients with liver metastasis (p < 0.01). Although MAGE-1 or -3 genes were not induced by DAC, MAGE-2 or -4 genes were induced in three of four MAGE-2 negative cell lines or three of seven MAGE-4 negative cell lines, respectively.
The MAGE genes were expressed exclusively in tumor tissues of one third of patients with colorectal carcinoma. The identification of such tumor rejection antigens is considered to uncover a new possibility for the specific immunotherapy of colorectal carcinoma. The demethylating agent may increase the number of patients who might be candidates for MAGE-specific immunotherapy.
人类基因MAGE - 1和- 3编码肿瘤特异性肽抗原,可被自体细胞毒性T淋巴细胞识别。这些基因编码的抗原可能对癌症免疫治疗有用。然而,关于这些基因在人类结直肠癌中的表达情况知之甚少。
采用逆转录聚合酶链反应测定54对结直肠癌肿瘤组织及相应正常组织标本中MAGE - 1、- 2和- 3基因的表达。还使用去甲基化剂5 - 氮杂- 2'-脱氧胞苷(DAC)检测了8种结肠癌细胞系中MAGE - 1、- 2、- 3和- 4基因表达的诱导情况。
在正常结直肠组织中完全未检测到MAGE基因的表达。在肿瘤组织标本中,分别有16例(30%)、15例(28%)和11例(20%)患者检测到MAGE - 1, - 2和- 3的表达。在肝转移患者中这种表达较为常见(p < 0.01)。虽然DAC未诱导MAGE - 1或- 3基因表达,但在4株MAGE - 2阴性细胞系中的3株或7株MAGE - 4阴性细胞系中的3株中分别诱导了MAGE - 2或- 4基因表达。
MAGE基因仅在三分之一的结直肠癌患者的肿瘤组织中表达。鉴定此类肿瘤排斥抗原被认为可为结直肠癌的特异性免疫治疗开辟新的可能性。去甲基化剂可能会增加可能成为MAGE特异性免疫治疗候选者的患者数量。