Xian W, Zheng H, Wu W J
The Third Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Genet Mol Res. 2015 Jul 13;14(3):7634-42. doi: 10.4238/2015.July.13.8.
We conducted a case-control study in a Chinese population to assess whether 5 common single-nucleotide polymorphisms in the vascular endothelial growth factor gene (VEGF) affect the risk of renal cell carcinoma (RCC). The study population included 266 RCC patients who were newly diagnosed and histologically confirmed to have RCC as well as 532 cancer-free controls. Genotyping of VEGF -2578C/A, -1156G/A, +1612G/A, +936C/T, and -634G/C was conducted by polymerase chain reaction-restriction fragment length polymorphism. RCC patients were more likely to have higher body mass index, and have a habit of tobacco smoking as well as suffer from diabetes. Conditional logistic regression analyses showed that individuals with the AA genotype and A allele of -2578C/A significantly increased the risk of RCC when compared with the CC genotype. Individuals carrying the CT and TT geno-types of +936C/T were correlated with an increased risk of RCC compared to the CC genotype. The T allele of +936C/T was associated with an increased risk of RCC. The -2578C/A and +936C/T polymorphisms in the VEGF gene may play a role in the etiology of RCC.
我们在中国人群中开展了一项病例对照研究,以评估血管内皮生长因子基因(VEGF)中的5种常见单核苷酸多态性是否会影响肾细胞癌(RCC)的发病风险。研究人群包括266例新诊断且经组织学确诊为肾细胞癌的患者以及532例无癌对照者。通过聚合酶链反应-限制性片段长度多态性方法对VEGF -2578C/A、-1156G/A、+1612G/A、+936C/T和-634G/C进行基因分型。肾细胞癌患者更有可能具有较高的体重指数、有吸烟习惯以及患有糖尿病。条件逻辑回归分析显示,与CC基因型相比,-2578C/A的AA基因型和A等位基因个体显著增加了肾细胞癌的发病风险。与CC基因型相比,携带+936C/T的CT和TT基因型个体与肾细胞癌发病风险增加相关。+936C/T的T等位基因与肾细胞癌发病风险增加相关。VEGF基因中的-2578C/A和+936C/T多态性可能在肾细胞癌的病因学中起作用。