Zhao Zigang, Ba Caixia, Wang Wei, Wang Xiaohong, Xue Ruizeng, Wu Xiaoting
Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, PR China.
Genet Test Mol Biomarkers. 2012 Dec;16(12):1390-4. doi: 10.1089/gtmb.2012.0266. Epub 2012 Sep 24.
Studies investigating the association between vascular endothelial growth factor (VEGF) polymorphisms and colorectal cancer (CRC) risk report conflicting results. To clarify the effect of four VEGF (-460T/C, -634G/C, +936C/T, and -2578C/A) gene polymorphisms on the risk of developing CRC, we carried out a meta-analysis using published data to obtain more precise estimates of risk.
Electronic searches of PubMed and EMBASE were conducted to select studies for this meta-analysis. The principal outcome measure was the odds ratio (OR) with 95% confidence interval (CI) for the risk of CRC associated with four VEGF (-460T/C, -634G/C, +936C/T, and -2578C/A) gene polymorphisms.
We identified 12 epidemiologic studies, which included 2770 CRC cases and 2568 controls. The combined results based on all studies showed that CRC cases had a significantly higher frequency of VEGF -634GG (OR=1.24, 95% CI=1.06, 1.44) and -2578AA (OR=1.37, 95% CI=1.12, 1.66) genotype and a lower frequency of -634CG (OR=0.82, 95% CI=0.71, 0.95) than controls. When stratifying for race, we found that patients with CRC had a significantly higher frequency of -460TC (OR=1.54, 95% CI=1.22, 1.94), -460CC (OR=2.00, 95% CI=1.50, 2.67), and -2578AA (OR=1.38, 95% CI=1.12, 1.69) and a lower frequency of -2578AA (OR=0.78, 95% CI=0.65, 0.93) genotypes of VEGF than controls, among Caucasians. We also found that patients with CRC had a significantly higher frequency of -634GG (OR=1.61, 95% CI=1.20, 2.15) and a lower frequency of -634CG (OR=0.60, 95% CI=0.46, 0.79) genotypes of VEGF than controls, among Asians.
Our meta-analysis suggests that the VEGF -460T/C, -634G/C, and -2578C/A gene polymorphisms are associated with a risk of CRC.
关于血管内皮生长因子(VEGF)基因多态性与结直肠癌(CRC)风险之间关联的研究结果相互矛盾。为了阐明VEGF四个基因多态性位点(-460T/C、-634G/C、+936C/T和-2578C/A)对患CRC风险的影响,我们利用已发表的数据进行了一项荟萃分析,以获得更精确的风险估计值。
通过对PubMed和EMBASE进行电子检索,筛选出用于该荟萃分析的研究。主要结局指标是与VEGF四个基因多态性位点(-460T/C、-634G/C、+936C/T和-2578C/A)相关的CRC风险的比值比(OR)及95%置信区间(CI)。
我们纳入了12项流行病学研究,其中包括2770例CRC病例和2568例对照。基于所有研究的综合结果显示,CRC病例中VEGF -634GG基因型(OR=1.24,95%CI=1.06,1.44)和-2578AA基因型(OR=1.37,95%CI=1.12,1.66)的频率显著高于对照组,而-634CG基因型(OR=0.82,95%CI=0.71,0.95)的频率低于对照组。按种族分层后,我们发现,在白种人中,CRC患者VEGF -460TC基因型(OR=1.54,95%CI=1.22,1.94)、-460CC基因型(OR=2.00,95%CI=1.50,2.67)和-2578AA基因型(OR=1.38,95%CI=1.12,1.69)的频率显著高于对照组,而-2578AA基因型(OR=0.78,95%CI=0.65,0.93)的频率低于对照组。我们还发现,在亚洲人中,CRC患者VEGF -634GG基因型(OR=1.61,95%CI=1.20,2.15)的频率显著高于对照组,而-634CG基因型(OR=0.60,95%CI=0.46,0.79)的频率低于对照组。
我们的荟萃分析表明,VEGF -460T/C、-634G/C和-2578C/A基因多态性与CRC风险相关。