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BAGE、GAGE和MAGE基因在人胃癌中的表达。

Expression of BAGE, GAGE, and MAGE genes in human gastric carcinoma.

作者信息

Li J, Yang Y, Fujie T, Baba K, Ueo H, Mori M, Akiyoshi T

机构信息

Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu 874, and Department of Surgery, Oita Prefectural Hospital, Oita 870, Japan.

出版信息

Clin Cancer Res. 1996 Sep;2(9):1619-25.

PMID:9816341
Abstract

The MAGE, BAGE, and GAGE genes code for distinct antigens that are recognized by autologous cytolytic T lymphocytes. We investigated the expression of these genes in both cell lines and surgical samples of gastric carcinoma, using reverse transcription-PCR. Furthermore, the induction of these genes by 5-aza-2'-deoxycytidine (DAC), a demethylating agent, was also examined in several cell lines. Of 11 cell lines, BAGE, GAGE1-6, GAGE1-2, MAGE-1, and MAGE-3 were detected in 7 (64%), 4 (36%), 3 (27%), 8 (73%), and 8 (73%) cell lines, respectively. After the in vitro treatment of the negative cell lines with DAC, the expression of these genes became positive in 46 to 91% of these cell lines. No expression of these genes was seen in any of the 57 samples of normal gastric tissue. In contrast, the tumor tissue samples expressed BAGE, GAGE1-6, GAGE1-2, MAGE-1, and MAGE-3 in 13 (23%), 9 (16%), 6 (11%), 25 (44%), and 23 (40%) tissue samples, respectively. Thus, at least one of these genes was expressed in 35 (61%) of 57 carcinomas. An analysis of the relationship between clinicopathological factors and the expression of these genes revealed that either BAGE or one of these genes was more frequently expressed in histologically intestinal-type than in diffuse-type carcinomas. Our results suggest that, because of the higher expression of these genes and the possible induction of these genes by DAC, patients with gastric carcinoma may, therefore, be potential candidates for tumor-specific immunotherapy directed against these antigens.

摘要

MAGE、BAGE和GAGE基因编码的独特抗原可被自体溶细胞性T淋巴细胞识别。我们使用逆转录聚合酶链反应研究了这些基因在胃癌细胞系和手术样本中的表达。此外,还在几种细胞系中检测了去甲基化剂5-氮杂-2'-脱氧胞苷(DAC)对这些基因的诱导作用。在11种细胞系中,分别在7种(64%)、4种(36%)和3种(27%)细胞系中检测到了BAGE、GAGE1-6、GAGE1-2,在8种(73%)细胞系中检测到了MAGE-1和MAGE-3。在用DAC对阴性细胞系进行体外处理后,这些基因在46%至91%的细胞系中表达变为阳性。在57份正常胃组织样本中均未检测到这些基因的表达。相比之下,肿瘤组织样本中分别有13份(23%)、9份(16%)、6份(11%)、25份(44%)和23份(40%)组织样本表达了BAGE、GAGE1-6、GAGE1-2、MAGE-1和MAGE-3。因此,在57例癌组织中有35例(61%)表达了这些基因中的至少一种。对临床病理因素与这些基因表达之间关系的分析表明,BAGE或这些基因中的一种在组织学上的肠型癌中比弥漫型癌中更频繁地表达。我们的结果表明,由于这些基因的高表达以及DAC可能对这些基因的诱导作用,因此胃癌患者可能是针对这些抗原的肿瘤特异性免疫治疗的潜在候选者。

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