Kong UnHee, Koo JaYoung, Choi KyungHun, Park JongWook, Chang HeeKyung
Department of Pathology, Medical College of Kosin University, Korea.
Hepatogastroenterology. 2004 Sep-Oct;51(59):1519-23.
BACKGROUND/AIMS: There is still little information on the function of GAGE gene in stomach cancer except for cancer-specific gene expression recognized by autologous T lymphocytes. This study attempted to detect GAGE expression in stomach cancer to evaluate its clinical implication as a tumor marker or prognosticator as well as to find the candidate for immunotherapy.
Tumor samples from 60 patients and gastric juices from 18 patients with gastric cancer were studied by using RT-PCR with common primer. In-situ RT-PCR and southern blotting were performed to confirm the RT-PCR products.
No expression of GAGE was observed in non-neoplastic juices and tissues. Fifteen out of 60 tumor tissues expressed GAGE (25.0%) mRNA, of which 13 cases (86.7%) were intestinal type and only 2 cases (13.3%) were diffuse type. In gastric juice, 22.2% (4/18) showed mRNA expression, all of which were intestinal type. GAGE expressions in both cancer tissues and gastric juices had a significant tendency to be higher by stage and lymph node metastasis (p<0.05). However, they did not show a significant relationship with tumor cell differentiation and vascular and perineural invasions.
These results suggest that GAGE gene might have an important role in the development and progression of intestinal type of stomach cancer and the detection of GAGE mRNA may be eligible to the panel of molecular markers for aggressive behavior as well as being useful to a molecule for cancer-specific immunotherapy.
背景/目的:除了自体T淋巴细胞识别的癌症特异性基因表达外,关于GAGE基因在胃癌中的功能仍知之甚少。本研究试图检测胃癌中GAGE的表达,以评估其作为肿瘤标志物或预后指标的临床意义,并寻找免疫治疗的候选物。
采用通用引物通过逆转录聚合酶链反应(RT-PCR)对60例患者的肿瘤样本和18例胃癌患者的胃液进行研究。进行原位RT-PCR和Southern印迹以确认RT-PCR产物。
在非肿瘤性胃液和组织中未观察到GAGE的表达。60例肿瘤组织中有15例(25.0%)表达GAGE mRNA,其中13例(86.7%)为肠型,仅2例(13.3%)为弥漫型。在胃液中,22.2%(4/18)显示mRNA表达,均为肠型。癌组织和胃液中的GAGE表达均有随分期和淋巴结转移而显著升高的趋势(p<0.05)。然而,它们与肿瘤细胞分化以及血管和神经周围侵犯无显著关系。
这些结果表明,GAGE基因可能在肠型胃癌的发生和发展中起重要作用,检测GAGE mRNA可能适用于作为侵袭性行为的分子标志物组合,并且对癌症特异性免疫治疗的分子也有用。