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机构地区:[1]苏州大学附属第四医院肿瘤研究所,无锡214062
出 处:《肿瘤》2008年第12期1086-1089,共4页Tumor
基 金:无锡市社会发展科技指导性计划项目(编号:CLZ00612)
摘 要:目的:研究胸苷酸合成酶(thymidylate synthase,TS)基因增强子区(enhancer region,ER)串联重复序列多态和3’端非翻译区(untranslated region,UTR)6bp缺失或插入多态(del6/ins6)对接受以氟尿嘧啶(fluorouracil,FU)为基础的辅助化疗胃癌患者预后的影响。方法:116例经确诊的胃癌患者,采用以FU为基础的方案进行辅助化疗。应用PCR技术检测TS基因多态。结果:在116例胃癌患者中,TSER 2R/2R、2R/3R和3R/3R基因型频率分别为7.8%(9/116)、31.9%(37/116)和60.3%(70/116);TS ins6/ins6、ins6/del6和del6/del6基因型频率分别为9.5%(11/116)、41.4%(48/116)和49.1%(57/116)。携带ins6/ins6基因型患者的总生存期显著短于携带del6/del6(P=0.017)或ins6/del6基因型患者的生存期(P=0.022),不同TSER基因型胃癌患者的中位无复发生存期差异无统计学意义(P>0.05)。COX多因素分析结果显示,ins6/ins6基因型患者的死亡风险增加。结论:TS 3’-UTR ins6/del6基因多态性是接受以FU为基础的辅助化疗胃癌患者的独立预后因素。Objective: To investigate the effects of the tandem repeat polymorphisms in the enhancer region (ER) of thymidylate synthase (TS) gene and the 6-bp deletion/insertion (de16/ins6) polymorphism in the 3' untranslated region (3' -UTR) of TS gene on the clinical outcomes of gastric cancer patients treated with 5-FU-based adjuvant chemotherapy. Methods : One hundred and sixteen patients with gastric cancer were treated with 5-FU-based adjuvant chemotherapy. The polymorphisms of TSER and TS 3' -UTR in those patients were determined by polymerase chain reaction (PCR) method. Results: Of the 116 patients, the frequencies of the TSER 2R/ 2R, 2R/3R and 3R/3R were 7.8% (9/116) , 31.9% (37/116) , and 60.3% (70/116) , respectively; the frequencies of the TS 3' UTR ins6/ins6, ins6/de16 and del6/de16 were 9.5% (11/116) , 41.4% (48/116) and 49.1% (57/116) , respectively. The median survival period in ins6/ins6 carriers was significantly shorter than that of del6/de16 ( P = 0.017 ) or ins6/de16 ( P = 0.022 ) carriers. There was no significant difference in median relapse-free survival period between different TSER carriers ( P 〉 0.05 ). COX multivariate analysis showed that the ins6/ins6 carriers had increased death risk ( P 〈 0.05 ) compared to the other two genotypes. The median no-recurrence survival period had no statistical difference between them. Conclusion: The polymorphism of TS 3 UTR ins6/de16 may he an independent factor for the prognosis of gastric cancer patients treated with 5-FU-based adjuvant chemotherapy.
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