Chen Guo-Qiang, Luo Jian-bin, Wang Guang-Zhi, Ding Jin-E
Department of Urology, Second Hospital of Longyan City, Longyan, 364000, Fujian Province, China,
Tumour Biol. 2014 Mar;35(3):1875-9. doi: 10.1007/s13277-013-1250-9. Epub 2013 Dec 19.
Vascular endothelial growth factor (VEGF) plays a crucial role in the regulation of angiogenesis and is involved in the development and metastasis of common cancers. There were several case-controls studies published to assess the associations of VEGF polymorphisms with risk of prostate cancer, but the findings were inconsistent. We performed a meta-analysis to provide a comprehensive assessment of the associations of three VEGF polymorphisms with risk of prostate cancer. The pooled odds ratio (OR) with 95% confidence interval (95% CI) was calculated to assess the associations. Eleven individual case-control studies with a total of 5,209 cases of prostate cancer and 5,233 controls were finally included into our meta-analysis. Overall, VEGF rs833061 polymorphism was not associated with risk of prostate cancer (T versus C, OR = 1.14, 95% CI 0.91-1.44, P = 0.26; TT versus CC, OR = 1.09, 95% CI 0.67-1.76, P = 0.74; TT versus
CC/CT: OR = 1.46, 95% CI 0.67-3.18, P = 0.34; TT/CT versus CC, OR = 1.08, 95% CI 0.82-1.43, P = 0.59). VEGF rs3025039 polymorphism was also not associated with risk of prostate cancer (T versus C, OR = 1.03, 95% CI 0.91-1.16, P = 0.66; TT versus CC, OR = 1.82 95% CI 0.16-20.53, P = 0.63; TT versus CC/CT, OR = 2.00, 95% CI 0.18-22.41, P = 0.57; TT/CT versus CC, OR = 0.72, 95% CI 0.38-1.36, P = 0.31). VEGF rs2010963 polymorphism was not associated with risk of prostate cancer under three models (C versus G, OR = 1.17, 95% CI 0.92-1.48, P = 0.20; CC versus GG, OR = 2.28, 95% CI 0.90-5.75, P = 0.08; CC versus GG/GC, OR = 1.57, 95% CI 0.67-3.68, P = 0.30). In conclusison, current data suggest that those three VEGF polymorphisms are not obviously associated with risk of prostate cancer.
血管内皮生长因子(VEGF)在血管生成调节中起关键作用,并参与常见癌症的发生和转移。已有多项病例对照研究发表,以评估VEGF基因多态性与前列腺癌风险的关联,但研究结果并不一致。我们进行了一项荟萃分析,以全面评估三种VEGF基因多态性与前列腺癌风险的关联。计算合并比值比(OR)及95%置信区间(95%CI)以评估关联。最终,11项个体病例对照研究共5209例前列腺癌病例和5233例对照纳入我们的荟萃分析。总体而言,VEGF rs833061基因多态性与前列腺癌风险无关(T与C相比,OR = 1.14,95%CI 0.91 - 1.44,P = 0.26;TT与CC相比,OR = 1.09,95%CI 0.67 - 1.76,P = 0.74;TT与CC/CT相比:OR = 1.46,95%CI 0.67 - 3.18,P = 0.34;TT/CT与CC相比,OR = 1.08,95%CI 0.82 - 1.43,P = 0.59)。VEGF rs3025039基因多态性也与前列腺癌风险无关(T与C相比,OR = 1.03,95%CI 0.91 - 1.16,P = 0.66;TT与CC相比,OR = 1.82,95%CI 0.16 - 20.53,P = 0.63;TT与CC/CT相比,OR = 2.00,95%CI 0.18 - 22.41,P = 0.57;TT/CT与CC相比,OR = 0.72,95%CI 0.38 - 1.36,P = 0.31)。在三种模型下,VEGF rs2010963基因多态性与前列腺癌风险无关(C与G相比,OR = 1.17,95%CI 0.92 - 1.48,P = 0.20;CC与GG相比,OR = 2.28,95%CI 0.90 - 5.75,P = 0.08;CC与GG/GC相比,OR =