Mu Li-Na, Cao Wei, Zhang Zuo-Feng, Cai Lin, Jiang Qing-Wu, You Nai-Chieh, Goldstein Binh Yang, Wei Guo-Rong, Chen Chuan-Wei, Lu Qing-Yi, Zhou Xue-Fu, Ding Bao-Guo, Chang Jun, Yu Shun-Zhang
Department of Epidemiology, Fudan University School of Public Health, Shanghai, China.
Cancer Causes Control. 2007 Aug;18(6):665-75. doi: 10.1007/s10552-007-9012-x. Epub 2007 May 15.
Methylenetetrahydrofolate reductase (MTHFR), which is expressed in the liver, may be involved in both DNA methylation and DNA synthesis. It is also indicated as a potential risk factor of liver cancer in patients with chronic liver disease. To date, no study has been conducted on MTHFR and hepatocellular carcinoma (HCC) using a population-based design. The objective of this study was to evaluate the effects of polymorphisms of the MTHFR gene on the risk of primary liver cancer and their possible effect modifications on various environmental risk factors.
A population-based case-control study was conducted in Taixing, China. MTHFR C677T and A1298C were assayed by PCR-RFLP techniques.
The frequency of MTHFR 677 C/C wild homozygotes genotype was 25.8% in cases, which was lower than that in controls (34.5%). The adjusted odds ratios (ORs) for the MTHFR 677 C/T and T/T genotype were 1.66(95% CI: 1.06-2.61), 1.21(95% CI: 0.65-2.28) respectively when compared with the MTHFR 677 C/C genotype. Subjects carrying any T genotype have the increased risk of 1.55(95% CI: 1.01-2.40) for development of primary hepatocellular carcinoma. A high degree of linkage disequilibrium was observed between the C677T and A1298C polymorphisms, with the D' of 0.887 and p < 0.01. The MTHFR 677 any T genotype was suggested to have potentially more than multiplicative interactions with raw water drinking with p-value for adjusted interaction of 0.03.
We observed that the MTHFR 677 C/T genotype was associated with an increased risk of primary liver cancer in a Chinese population. The polymorphism of MTHFR 677 might modify the effects of raw water drinking on the risk of primary hepatocellular carcinoma.
亚甲基四氢叶酸还原酶(MTHFR)在肝脏中表达,可能参与DNA甲基化和DNA合成。它也被认为是慢性肝病患者患肝癌的潜在危险因素。迄今为止,尚未有基于人群设计的关于MTHFR与肝细胞癌(HCC)的研究。本研究的目的是评估MTHFR基因多态性对原发性肝癌风险的影响以及它们对各种环境危险因素可能的效应修饰作用。
在中国泰兴进行了一项基于人群的病例对照研究。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术检测MTHFR C677T和A1298C。
病例组中MTHFR 677 C/C野生纯合子基因型频率为25.8%,低于对照组(34.5%)。与MTHFR 677 C/C基因型相比,MTHFR 677 C/T和T/T基因型的校正比值比(OR)分别为1.66(95%可信区间:1.06 - 2.61)、1.21(95%可信区间:0.65 - 2.28)。携带任何T基因型的受试者发生原发性肝细胞癌的风险增加1.55(95%可信区间:1.01 - 2.40)。在C677T和A1298C多态性之间观察到高度连锁不平衡,D'为0.887,p < 0.01。MTHFR 677任何T基因型与饮用生水之间可能存在潜在的大于相乘的交互作用,校正交互作用的p值为0.03。
我们观察到MTHFR 677 C/T基因型与中国人群原发性肝癌风险增加相关。MTHFR 677多态性可能修饰饮用生水对原发性肝细胞癌风险的影响。