Lin Jie, Spitz Margaret R, Wang Yunfei, Schabath Matthew B, Gorlov Ivan P, Hernandez Ladia M, Pillow Patricia C, Grossman H Barton, Wu Xifeng
Department of Epidemiology, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Carcinogenesis. 2004 Sep;25(9):1639-47. doi: 10.1093/carcin/bgh175. Epub 2004 Apr 29.
Epidemiological studies have shown an association between low folate intake and an increased cancer risk. Major genes involved in folate metabolism include methylene-tetrahydrofolate reductase (MTHFR) and methionine synthase (MS). We investigated joint effects of polymorphisms of the MTHFR (677 C-->T, 1298A-->C) and MS genes (2756 A-->G), dietary folate intake and cigarette smoking on the risk of bladder cancer in a case-control study. The study population consisted of 457 bladder cancer patients and 457 healthy controls, matched to the cases in terms of age, gender and ethnicity. Genotype data were analyzed in a subset of 410 Caucasian cases and 410 controls. Compared with individuals carrying the MTHFR 677 wild-type (CC) and reporting a high folate intake, those carrying the variant genotype (CT or TT) and reporting a low folate intake were at a significantly 3.51-fold increased risk of bladder cancer (95% CI: 1.59-6.52). In contrast, individuals carrying a variant genotype and reporting a high folate intake were at only a 1.39-fold increased risk (95% CI: 0.71-2.70), and those carrying the wild-type and reporting a low folate intake were at only 1.56-fold increased risk (95% CI: 0.82-2.97). The interaction between genetic polymorphisms and folate intake was significant on the multiplicative scale (P = 0.01). When analyzed in the context of smoking status, compared with never smokers with the MTHFR 677 wild-type, the risk increased to 6.56-fold (95% CI: 3.28-13.12) in current smokers carrying the variant genotype. Analyses of the MTHFR 1298, MS 2756 genes revealed similar results. In addition, age at cancer onset in former smokers increased as the proportion of the heteromorphic haplotype in the individual increased (P = 0.005). Our results strongly suggest that polymorphisms of the MTHFR and MS genes act together with low folate intake and smoking to increase bladder cancer risk. These results have important implications for cancer prevention in susceptible populations.
流行病学研究表明,低叶酸摄入量与癌症风险增加之间存在关联。参与叶酸代谢的主要基因包括亚甲基四氢叶酸还原酶(MTHFR)和甲硫氨酸合成酶(MS)。在一项病例对照研究中,我们调查了MTHFR基因多态性(677C→T、1298A→C)和MS基因多态性(2756A→G)、膳食叶酸摄入量以及吸烟对膀胱癌风险的联合影响。研究人群包括457例膀胱癌患者和457名健康对照,在年龄、性别和种族方面与病例相匹配。对410例白种人病例和410名对照的一个亚组进行了基因型数据分析。与携带MTHFR 677野生型(CC)且报告叶酸摄入量高的个体相比,携带变异基因型(CT或TT)且报告叶酸摄入量低的个体患膀胱癌的风险显著增加3.51倍(95%可信区间:1.59 - 6.52)。相比之下,携带变异基因型且报告叶酸摄入量高的个体患癌风险仅增加1.39倍(95%可信区间:0.71 - 2.70),而携带野生型且报告叶酸摄入量低的个体患癌风险仅增加1.56倍(95%可信区间:0.82 - 2.97)。基因多态性与叶酸摄入量之间的相互作用在相乘尺度上具有显著性(P = 0.01)。在吸烟状况背景下进行分析时,与携带MTHFR 677野生型的从不吸烟者相比,携带变异基因型的当前吸烟者的风险增加到6.56倍(95%可信区间:3.28 - 13.12)。对MTHFR 1298、MS 2756基因的分析得出了类似结果。此外,既往吸烟者的癌症发病年龄随着个体中异型单倍型比例的增加而增加(P = 0.005)。我们的结果有力地表明,MTHFR和MS基因的多态性与低叶酸摄入量和吸烟共同作用,增加了膀胱癌风险。这些结果对易感人群的癌症预防具有重要意义。