Urology Department, CHRU de Tours, Tours, France.
J Urol. 2010 Oct;184(4):1273-8. doi: 10.1016/j.juro.2010.06.009. Epub 2010 Aug 17.
Vascular endothelial cell growth factor is studied in different malignant tumors as a key endothelial cell mitogen. Many single nucleotide polymorphisms in the VEGF gene have been described. We compared VEGF gene polymorphisms between a control group and a renal cancer group.
This study was performed in 202 control, white, healthy blood donors (control group) and in 51 consecutive patients with renal cell carcinoma. We studied VEGF genotype polymorphisms at positions -2549, -460, -1154, +405 and +936 using polymerase chain restriction fragment length polymorphism, and looked for correlations with clinical data.
No association was found between VEGF gene polymorphism and renal cell carcinoma prognostic parameters. However, in contrast as observed for controls and other polymorphisms the patient group displayed a heterozygote excess (p = 0.0179, 35.9% more than that expected) at the -460 polymorphism. Comparing the control group and the renal cell carcinoma group we detected a significantly increased risk of renal cell carcinoma in subjects with the C-460T polymorphism. T carrier genotypes and the T allele increased the risk of renal cell carcinoma with an OR of 14.15 (95% CI 1.900-105.41, p = 0.0017) and 2.14 (95% CI 1.34-3.419, p = 0.0018), respectively. The genotype at the -2549 polymorphism exhibited a nonsignificant trend for increased risk but the D allele was significantly associated with increased risk (p = 0.0305).
Our results suggest that the -460 polymorphism is a risk factor for renal cancer. An individual screening test could be proposed for high risk populations.
血管内皮生长因子 (VEGF) 作为关键的内皮细胞有丝分裂原,在不同的恶性肿瘤中进行研究。VEGF 基因的许多单核苷酸多态性已被描述。我们比较了对照组和肾癌组之间 VEGF 基因多态性。
这项研究在 202 名白种健康献血者(对照组)和 51 名连续的肾癌患者中进行。我们使用聚合酶链反应限制片段长度多态性研究了 VEGF 基因在位置-2549、-460、-1154、+405 和+936 的基因型多态性,并寻找与临床数据的相关性。
VEGF 基因多态性与肾癌的预后参数之间没有相关性。然而,与其他多态性相反,患者组在-460 多态性中显示出杂合子过多(p = 0.0179,比预期多 35.9%)。将对照组和肾癌组进行比较,我们发现 C-460T 多态性的个体患肾癌的风险显著增加。T 载体基因型和 T 等位基因使肾癌的风险增加 14.15 倍(95%CI 1.900-105.41,p = 0.0017)和 2.14 倍(95%CI 1.34-3.419,p = 0.0018)。-2549 多态性的基因型显示出风险增加的趋势,但无统计学意义,而 D 等位基因与风险增加显著相关(p = 0.0305)。
我们的结果表明-460 多态性是肾癌的一个危险因素。对于高危人群,可以提出个体筛查试验。