Ke Qiao, Liang Jie, Wang Li-Na, Hu Zhi-Bin, Jin Guang-Fu, Zhou Yan, Wang Jian-Ming, Tan Yong-Fei, Hua Zhao-Lai, Xu Yao-Chu, Shen Jing, Shen Hong-Bing
Department of Epidemiology and Biostatistics, Nanjing Medical University School of Public Health, Nanjing, China.
Mol Carcinog. 2008 Aug;47(8):647-51. doi: 10.1002/mc.20435.
Vascular endothelial growth factor (VEGF), the key mediator of angiogenesis, plays an important role in the development of different kind of tumors, including gastric cancer (GC). The aim of this study is to test the hypothesis that genetic variants of VEGF are associated with risk of GC. We genotyped four potentially functional polymorphisms (-2578C > A, -1498T > C, -634G > C, and +936C > T) of the VEGF gene in a population-based case-control study of 540 GC cases and 561 frequency-matched cancer-free controls in a high risk Chinese population. We found that none of the four polymorphisms or their haplotypes achieved significant difference in their distributions between GC cases and controls. Multiple logistic regression analyses revealed that GC risk was not significantly associated with the variant genotypes of the four VEGF polymorphisms as compared with their wild-type genotypes. In conclusion, our data did not support a significant association between VEGF SNPs and the risk of GC.
血管内皮生长因子(VEGF)是血管生成的关键介质,在包括胃癌(GC)在内的多种肿瘤发展中起重要作用。本研究的目的是检验VEGF基因变异与GC风险相关的假设。在一项基于人群的病例对照研究中,我们对540例GC病例和561例频率匹配的无癌对照进行了VEGF基因的四个潜在功能性多态性(-2578C>A、-1498T>C、-634G>C和+936C>T)的基因分型,该研究针对的是高危中国人群。我们发现,这四个多态性及其单倍型在GC病例和对照之间的分布均未达到显著差异。多因素逻辑回归分析显示,与野生型基因型相比,GC风险与四个VEGF多态性的变异基因型无显著关联。总之,我们的数据不支持VEGF单核苷酸多态性与GC风险之间存在显著关联。