首页> 外文期刊>Cancer genomics & proteomics >Interaction of methylenetetrahydrofolate reductase genotype and smoking habit in Taiwanese lung cancer patients.
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Interaction of methylenetetrahydrofolate reductase genotype and smoking habit in Taiwanese lung cancer patients.

机译:台湾肺癌患者亚甲基四氢叶酸还原酶基因型与吸烟习惯的相互作用。

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摘要

The aim of this study was to evaluate the association and interaction of genotypic polymorphisms in methylenetetrahydrofolate reductase (MTHFR) and environmental factors with lung cancer in Taiwan. Two well-known polymorphic variants of MTHFR, C677T (rs1801133) and A1298C (rs1801131), were analyzed in association with lung cancer susceptibility, and discussed their joint effects with individual habits on lung cancer risk. PATIENTS AND METHODS: In total, 358 patients with lung cancer and 716 healthy controls recruited from the China Medical Hospital in central Taiwan were genotyped. RESULTS: The MTHFR C677T genotype, but not the A1298C, was differently distributed between the lung cancer and control groups. The T allele of MTHFR C677T was significantly more frequently found in controls than in cancer patients. As for A1298C polymorphism, there was no difference in distribution between the lung cancer and control groups. Gene interactions with smoking were significant for MTHFR C677T polymorphism. The MTHFR C677T CT and TT genotypes in association with smoking conferred a decreased risk of 0.706 (95% confidence interval=0.531-0.939) for lung cancer. CONCLUSION: Our results provide the first evidence that the C allele of MTHFR C677T may be associated with the development of lung cancer and may be a novel useful marker for primary prevention and anticancer intervention.
机译:本研究的目的是评估台湾地区亚甲基四氢叶酸还原酶(MTHFR)基因型多态性与环境因素的关联和相互作用。分析了MTHFR的两个众所周知的多态性变体C677T(rs1801133)和A1298C(rs1801131),并与肺癌易感性相关联,并讨论了它们与个体习惯对肺癌风险的联合影响。病人和方法:总共从台湾中部中华医院招募的358例肺癌患者和716名健康对照者进行了基因分型。结果:MTHFR C677T基因型(而非A1298C)在肺癌组和对照组之间的分布不同。与癌症患者相比,在对照组中发现MTHFR C677T的T等位基因的频率更高。至于A1298C多态性,肺癌与对照组之间的分布没有差异。基因与吸烟的相互作用对于MTHFR C677T多态性具有重要意义。 MTHFR C677T CT和TT基因型与吸烟相关,使肺癌的风险降低了0.706(95%置信区间= 0.531-0.939)。结论:我们的结果提供了第一个证据,表明MTHFR C677T的C等位基因可能与肺癌的发生有关,并且可能是一级预防和抗癌干预的新型有用标记。

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