期刊文献+

亚甲基四氢叶酸还原酶C667T基因多态性与晚期胃癌患者对5-FU化疗疗效的相关性 被引量:5

Relationship between methylenetetrahydrofolate reductase polymorphism and clinical outcomes of advanced gastric cancer patients treated with 5-FU-based chemotherapy
原文传递
导出
摘要 目的观察亚甲基四氢叶酸还原酶(MTHFR)C667T基因多态性与5-氟尿嘧啶(5-FU)为基础的化疗方案治疗晚期胃癌的疗效间的关系。方法收集经病理学确诊的晚期胃癌59例。所有病例化疗前抽取外周静脉血,提取DNA,用连接酶检测反应技术(LDR)检测研究对象的MTHFR基因型。所有患者经5-FU为基础的联合化疗方案化疗。结果 59例晚期胃癌患者中,21例(35.59%)为MTHFRC/C基因型,22例(37.29%)为MTHFRC/T基因型,16例(27.12%)为MTHFRT/T基因型。其中,4例CR,14例PR,19例SD,22例PD,总有效率为30.51%(18/59)。MTHFRT/T基因型患者的化疗有效率(68.75%)明显高于C/T基因型患者(18.18%)(P<0.01),也明显高于C/C基因型(14.29%)(P<0.01)。结论 MTHFR基因型对预测以5-FU为基础化疗方案治疗晚期胃癌的疗效具有较好的临床意义。 Objective To investigate the relationship between the methylenetetrahydrofolate reductase(MTHFR) polymorphism and the response to 5-fluoropyrimidine(FU)-based chemotherapy in advanced gastric cancer(AGC).Methods DNAs of peripheral blood leukocytes from 59 patients with AGC were obtained before therapy and analyzed for MTHFR genotypes by PCR-LDR method.All patients were treated with 5-FU-based chemotherapy.Results Of 59 AGC cases with MTHFR C677T genotype,the frequency of C/C was 35.59%,C/T was 37.79% and T/T was 27.12%.Total response rate of chemotherapy was 30.51%,including 4 patients with complete response,14 with partial response,19 with stable disease and 22 with progressive disease.However,the response rate in patients with T/T genotype (68.75%) was significantly higher than either the patients with C/T genotype(18.18%) (P0.01) or with C/C genotype(14.29%)(P0.01).Conclusion MTHFR C677T polymorphism can predict the effects of 5-FU-based chemotherapy in AGC.
出处 《江苏医药》 CAS CSCD 北大核心 2010年第18期2125-2127,共3页 Jiangsu Medical Journal
基金 常州市卫生局重大招标课题(ZD200810)
关键词 晚期胃癌 亚甲基四氢叶酸还原酶 5-氟尿嘧啶 Advanced gastric cancer Methylenetetrahydrofolate reductase 5-fluoropyrimidine
  • 相关文献

参考文献16

  • 1Rosenblatl DS. Methylenetetrahydrofolate reductase[J]. Clin Invest Med,2001,24(1):56- 59.
  • 2Shen H,Xu Y,Zheng Y, et al. Polymorphisms of 5,10 methylenetetrahydrofolate reductase and risk of gastric cancer in a Chinese population: a case-control study. [J]. Int J Cancer 2001,95 (5): 332-336.
  • 3Demchinskaya AV,Shilov IA,Karyagina AS. A new approach for point mutation detection based on a tigase chain reaction [J]. J Biochem Biophys Methods, 2001,50 (1) : 79-89.
  • 4Boccia S, Hung R, Ricciardi G, et al. Meta- and pooled analyses of the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and gastric cancer risk:a huge-GSEC review[J]. Am J Epidemiol, 2008,167(5) : 505-516.
  • 5Zintzaras E. Association of methylenetetrahydrofolate reductase (MTHFR) polymorphisms with genetic susceptibility to gastric cancer: a meta analysis[J]. Hum Genet, 2006,51 (7):618-624.
  • 6Larsson SC,Giovannucci E,Wolk A. Folate intake, MTHFR polymorphisms,and risk of esophageal,gastric, and pancreatic cancer:a meta-analysis[J]. Gastroenterology, 2006, 131 (4) 1271-1283.
  • 7Botto LD, Yang Q. 5, 10-Methylenetetrahydrofotate reduetase gene variants and congenital anomalies: a huge review [J]. Am J Epidemiol, 2000,151(9) :862-877.
  • 8Kin: DH. The interactive effect of methyl group diet and polymorphism of methylenetetrahydrofolate reductase on the risk of colorectal cancer[J]. Mutat Res,2007,622(1): 14-18.
  • 9Larsson SC, Giovannucci E,Wolk A. Folate intake, MTHFR polymorphisms, and risk of esophageal, gastric, and pancreatic cancer: a meta-analysis[J]. Gastroenterology, 2006, 131 (4) : 1271-1283.
  • 10Ulvik A, Ueland PM, Fredriksen A, et al. Functional inference of the methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphisms from a large-scale epidemiological study[J]. Hum Genet, 2007,121(1) : 57-64.

同被引文献41

引证文献5

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部