Department of Preventive Medicine, Chonnam National University Medical School, Gwangju, South Korea.
BMC Cancer. 2010 May 26;10:236. doi: 10.1186/1471-2407-10-236.
This study was designed to investigate an association between the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and the risk of gastric and colorectal cancer in the Korean population.
We conducted a population-based large-scale case-control study involving 2,213 patients with newly diagnosed gastric cancer, 1,829 patients with newly diagnosed colorectal cancer, and 1,700 healthy controls. Genotyping was performed with peripheral blood DNA for MTHFR C677T polymorphisms. The statistical significance was estimated by logistic regression analysis.
The MTHFR C677T frequencies of CC, CT, and TT genotypes were 35.2%, 47.5%, and 17.3% among stomach cancer, 34%, 50.5%, and 15.5% in colorectal cancer, and 31.8%, 50.7%, and 17.5% in the controls, respectively. The MTHFR 677TT genotype showed a weak opposite association with colorectal cancer compared to the homozygous CC genotype [adjusted age and sex odds ratio (OR) = 0.792, 95% confidence interval (CI) = 0.638-0.984, P = 0.035]. Subjects with the MTHFR 677CT showed a significantly reduced risk of gastric cancer compared whose with the 677CC genotype (age- and sex-adjusted OR = 0.810; 95% CI = 0.696-0.942, P = 0.006). We also observed no significant interactions between the MTHFR C677T polymorphism and smoking or drinking in the risk of gastric and colorectal cancer.
The T allele was found to provide a weak protective association with gastric cancer and colorectal cancer.
本研究旨在探讨亚甲基四氢叶酸还原酶(MTHFR)C677T 多态性与韩国人群胃癌和结直肠癌风险之间的关联。
我们进行了一项基于人群的大型病例对照研究,纳入了 2213 例新诊断的胃癌患者、1829 例新诊断的结直肠癌患者和 1700 例健康对照者。采用外周血 DNA 进行 MTHFR C677T 多态性基因分型。采用 logistic 回归分析估计统计学意义。
胃癌患者的 MTHFR C677T 基因型频率分别为 CC、CT 和 TT 基因型为 35.2%、47.5%和 17.3%,结直肠癌患者分别为 34%、50.5%和 15.5%,对照组分别为 31.8%、50.7%和 17.5%。与纯合 CC 基因型相比,MTHFR 677TT 基因型与结直肠癌呈弱负相关[校正年龄和性别比值比(OR)=0.792,95%置信区间(CI)=0.638-0.984,P=0.035]。与 677CC 基因型相比,MTHFR 677CT 基因型的受试者患胃癌的风险显著降低(校正年龄和性别后的 OR=0.810;95%CI=0.696-0.942,P=0.006)。我们还观察到,MTHFR C677T 多态性与吸烟或饮酒在胃癌和结直肠癌风险之间没有显著的交互作用。
T 等位基因与胃癌和结直肠癌呈弱保护关联。