Lee Su Jeong, Lee Sin Yeob, Jeon Hyo-Sung, Park Sun Ha, Jang Jin Sung, Lee Ga Young, Son Ji Woong, Kim Chang Ho, Lee Won Kee, Kam Sin, Park Rang Woon, Park Tae-In, Kang Young Mo, Kim In-San, Jung Tae Hoon, Park Jae Yong
Department of Biochemistry, School of Medicine, Kyungpook National University Hospital, Kyungpook National University, Daegu, Korea.
Cancer Epidemiol Biomarkers Prev. 2005 Mar;14(3):571-5. doi: 10.1158/1055-9965.EPI-04-0472.
Angiogenesis is an essential process in the development, growth, and metastasis of malignant tumors including lung cancer. DNA sequence variations in the vascular endothelial growth factor (VEGF) gene may lead to altered VEGF production and/or activity, thereby causing interindividual differences in the susceptibility to lung cancer via their actions on the pathways of tumor angiogenesis. To test this hypothesis, we investigated the potential association between three VEGF polymorphisms (-460T > C, +405C > G, and 936C > T)/haplotypes and the risk of lung cancer in a Korean population. VEGF genotypes were determined in 432 lung cancer patients and 432 healthy controls that were frequency matched for age and sex. VEGF haplotypes were predicted using Bayesian algorithm in the phase program. Compared with the combined +405 CC and CG genotype, the +405 GG genotype found associated with a significantly decreased risk of small cell carcinoma [SCC; adjusted odds ratio (OR), 0.36; 95% confidence interval (95% CI), 0.17-0.78]. The 936 CT genotype and the combined 936 CT and TT genotype were also associated with a significantly decreased risk of SCC compared with the 936 CC genotype (adjusted OR, 0.47; 95% CI, 0.26-0.85 and adjusted OR, 0.44; 95% CI, 0.24-0.80, respectively). Haplotype CGT was associated with a significantly decreased risk of SCC (adjusted OR, 0.39; 95% CI, 0.18-0.87), whereas haplotype TCC conferred a significantly increased risk of SCC (adjusted OR, 1.63; 95% CI, 1.14-2.33). None of the VEGF polymorphisms studied significantly influenced the susceptibility to lung cancer except SCC. However, haplotypes TCT and TGT were significantly associated with the risk of overall lung cancer, respectively (adjusted OR, 0.38; 95% CI, 0.25-0.60 and adjusted OR, 3.94; 95% CI, 2.00-7.76, respectively). These effects of haplotypes TCT and TGT on lung cancer risk were observed in three major histologic types of lung cancer. These results suggest that the VEGF gene may be contribute to an inherited predisposition to lung cancer.
血管生成是包括肺癌在内的恶性肿瘤发展、生长和转移过程中的一个重要过程。血管内皮生长因子(VEGF)基因的DNA序列变异可能导致VEGF产生和/或活性改变,从而通过其对肿瘤血管生成途径的作用,引起个体对肺癌易感性的差异。为了验证这一假设,我们在韩国人群中研究了三种VEGF多态性(-460T>C、+405C>G和936C>T)/单倍型与肺癌风险之间的潜在关联。在432例肺癌患者和432例年龄和性别频率匹配的健康对照中确定了VEGF基因型。使用相位程序中的贝叶斯算法预测VEGF单倍型。与+405 CC和CG基因型组合相比,发现+405 GG基因型与小细胞癌(SCC)风险显著降低相关[校正比值比(OR),0.36;95%置信区间(95%CI),0.17-0.78]。与936 CC基因型相比,936 CT基因型以及936 CT和TT基因型组合也与SCC风险显著降低相关(校正OR分别为0.47;95%CI,0.26-0.85和校正OR,0.44;95%CI,0.24-0.80)。单倍型CGT与SCC风险显著降低相关(校正OR,0.39;95%CI,0.18-0.87),而单倍型TCC使SCC风险显著增加(校正OR,1.63;95%CI,1.14-2.33)。除SCC外,所研究的VEGF多态性均未显著影响肺癌易感性。然而,单倍型TCT和TGT分别与总体肺癌风险显著相关(校正OR分别为0.38;95%CI,0.25-0.60和校正OR,3.94;95%CI,2.00-7.76)。在三种主要组织学类型的肺癌中均观察到单倍型TCT和TGT对肺癌风险的这些影响。这些结果表明,VEGF基因可能有助于肺癌的遗传易感性。