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首页> 外文期刊>Annals of Coloproctology >Association of Methylenetetrahydrofolate Reductase C677T, A1298C, and G1793A Polymorphism and the Risk of Colon Cancer
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Association of Methylenetetrahydrofolate Reductase C677T, A1298C, and G1793A Polymorphism and the Risk of Colon Cancer

机译:亚甲基四氢叶酸还原酶C677T,A1298C和G1793A多态性与结肠癌风险的关系

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Purpose Methylenetetrahydrofolate reductase (MTHFR) is a critical enzyme regulating folate level, which affects DNA synthesis and methylation. MTHFR is highly polymorphic, and its variant genotypes result in decreased MTHFR enzyme activity and lower plasma folate level. Generally, a low folate level is known to be associated with a gastrointestinal neoplasm. Three common single nucleotide polymorphisms (SNPs) resulting in amino-acid changes (C677T, A1298C and G1793A) have been reported in MTHFR. We studied the relationship of MTHFR C677T, A1298C and G1793A polymorphisms between from colon cancer group and control group of Korean people. Methods We performed a case-control study to examine the relationship between MTHFR C677, A1298C, and G1793A polymorphisms and the risk of colon cancer. Two hundred seven (207) individuals with colon cancer and 288 healthy persons were analyzed. Blood sampling of each group was performed, and (PCR-RFLP) was analyzed; as a result, MTHFR polymorphism genotypes were obtained. Results The genotype frequencies of MTHFR C677T polymorphisms were 27.1% (CC), 48.3% (CT), 24.6% (TT), and 72.9% (CT+TT) in the patient group and 39.2% (CC), 36.8% (CT), 24.0% (TT), and 60.8% (CT+TT) in the control group. The genotype frequencies of MTHFR A1298C polymorphisms were 58% (AA), 35.7% (AC), 6.3% (CC), and 42% (AC+CC) in the patient group and 55.6% (AA), 40.3% (AC), 4.2% (CC), and 44.4% (AC+CC) in control group. The genotype frequencies of MTHFR G1793A polymorphisms were 83% (GG), 15.9% (GA), 1% (AA), and 16.9% (GA+AA) in the patient group and 85.8% (GG), 11.8% (GA), 2.4% (AA), and 14.2% (GA+AA) in the control group. The 677CT genotype was associated with a significantly increased risk for colon cancer (adjusted OR=1.90, 95% confidence interval: 1.25~2.90 in CT) than the 677CC genotype. The 1298CC, 1298AC, 1793AA, and 1793GA genotypes were not associated with a significantly increased risk for colon cancer. Conclusions The MTHFR C677T polymorphism may influence colon cancer, but the MTHFR A1298C and G1793A polymorphisms need to be studied further for careful interpretation and confirmation in larger studies.
机译:目的亚甲基四氢叶酸还原酶(MTHFR)是调节叶酸水平的关键酶,可影响DNA合成和甲基化。 MTHFR是高度多态的,其变异的基因型导致MTHFR酶活性降低和血浆叶酸水平降低。通常,已知叶酸水平低与胃肠道肿瘤有关。在MTHFR中已经报道了导致氨基酸改变的三种常见的单核苷酸多态性(SNP)(C677T,A1298C和G1793A)。我们研究了韩国人结肠癌组和对照组中MTHFR C677T,A1298C和G1793A多态性的关系。方法我们进行了病例对照研究,以检查MTHFR C677,A1298C和G1793A多态性与结肠癌风险之间的关系。分析了二十七(207)名结肠癌患者和288名健康人。进行每组的血液采样,并进行(PCR-RFLP)分析。结果,获得了MTHFR多态性基因型。结果患者组中MTHFR C677T多态性的基因型频率分别为27.1%(CC),48.3%(CT),24.6%(TT)和72.9%(CT + TT),分别为39.2%(CC),36.8%(CT) ),对照组的24.0%(TT)和60.8%(CT + TT)。患者组中MTHFR A1298C多态性的基因型频率分别为58%(AA),35.7%(AC),6.3%(CC)和42%(AC + CC),以及55.6%(AA),40.3%(AC)对照组为4.2%(CC)和44.4%(AC + CC)。患者组中MTHFR G1793A多态性的基因型频率分别为83%(GG),15.9%(GA),1%(AA)和16.9%(GA + AA),分别为85.8%(GG),11.8%(GA)对照组为2.4%(AA)和14.2%(GA + AA)。与677CC基因型相比,677CT基因型与结肠癌风险显着相关(校正后的OR = 1.90,95%置信区间:1.25〜2.90)。 1298CC,1298AC,1793AA和1793GA基因型与结肠癌风险显着增加无关。结论MTHFR C677T多态性可能会影响结肠癌,但是MTHFR A1298C和G1793A多态性需要进一步研究,以便在较大的研究中进行仔细的解释和确认。

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