Genetic Polymorphism of MTHFR C677T Influences Susceptibility to HBV-Related Hepatocellular Carcinoma in a Chinese Population: a Case-Control Study

被引:11
|
作者
Qiao, Kunyan [1 ,2 ]
Zhang, Shitian [3 ]
Trieu, Congdoanh [4 ]
Dai, Qinghai [1 ,2 ]
Huo, Zhixiao [1 ,2 ]
Du, Yanan [5 ]
Lu, Wei [1 ,2 ,6 ]
Hou, Wei [1 ,2 ]
机构
[1] Tianjin Second Peoples Hosp, 7 Sudi South Rd, Tianjin, Peoples R China
[2] Tianjin Inst Hepatol, 7 Sudi South Rd, Tianjin, Peoples R China
[3] Tianjin Med Univ, Grad Sch, Tianjin, Peoples R China
[4] Tianjin Med Univ, Int Med Sch, Tianjin, Peoples R China
[5] Tsinghua Univ, Sch Med, Dept Biomed Engn, Beijing, Peoples R China
[6] Tianjin First Ctr Hosp, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
MTHFR; polymorphism; HBV; HCC; METHYLENETETRAHYDROFOLATE REDUCTASE MTHFR; LIVER-CANCER; RISK; ASSOCIATION; CIRRHOSIS; FOLATE; HCC;
D O I
10.7754/Clin.Lab.2016.161003
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Methylene tetrahydrofolate reductase (MTHFR) is the key enzyme of folic acid metabolism and the C677T mutation is associated with decreased enzyme activity. Several studies have shown its regulatory role in carcinogenesis and tumor growth. HBV (hepatitis B virus)-related HCC (hepatocellular carcinoma) is one of the most common liver cancers worldwide. Therefore, the present case-control study aimed to investigate the role of genetic polymorphism of MTHFR C677T in the development and progression of HBV-related HCC in a Chinese population. Methods: Subjects enrolled included 204 HBV-related HCC patients and 211 HBV infected patients without HCC. MTHFR C677T polymorphism was genotyped via a DNA microarray-based assay. The relationship between the MTHFR C677T polymorphism and HBV-related HCC was analyzed. Results: The genotype frequencies of MTHFR C677T were statistically different between the HCC and control groups (p = 0.025). The TT genotype was associated with elevated risk of HBV-related HCC in a Chinese population under different genetic models after an adjustment for age, gender, HBV infection duration, and HCC family history (T vs. C, OR = 1.462, 95% CI: 1.090 - 1.962, p = 0.011; TT vs. CC, OR = 2.151, 95% Cl: 1.143 - 4.049, p = 0.018; TT vs. CC+CT, OR = 1.918, 95% CI: 1.215 - 3.026, p = 0.005). When stratified with the known duration of HBV infection, subjects with HBV infection duration of more than 20 years and carrying the homozygous TT genotype had a higher susceptibility to HCC than those with the C allele (CC/CT) (OR = 2.568, 95% Cl: 1.244 - 5.303; p = 0.011). There was no significant association between MTHFR C677T genotypes and HCC stages based on BCLC staging system. Conclusions: MTHFR C677T polymorphism with TT genotype could be a factor that increases the risk of HBV-related HCC in a Chinese population, especially those with HBV infection duration of more than 20 years.
引用
收藏
页码:787 / 795
页数:9
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