Diao Jingfang, Bao Jie, Peng Jianxin, Mo Jiaqiang, Ye Qing, He Junming
Department of Hepatobiliary Surgery, Second Affiliated Hospital of Guangzhou University of Chinese Medicine (Guangdong Provincial Hospital of TCM), Guangzhou, People's Republic of China.
Department of Internal Medicine, Hospital of South China Normal University, Guangzhou, People's Republic of China.
Ther Adv Med Oncol. 2017 Jan;9(1):13-21. doi: 10.1177/1758834016668682. Epub 2016 Sep 18.
NAD(P)H: quinone oxidoreductase 1 (NQO1) C609T gene polymorphisms have been reported to influence the risk for esophageal cancer (EC) in many studies. However, the results remain controversial and ambiguous. We performed a meta-analysis, which included 13 independent studies with a total of 2357 subjects, to examine the association between NQO1 C609T polymorphism and EC. The association was assessed by five different gene models. The overall analysis suggested that the variant allele and genotypes were significantly related to increased risk of EC (odds ratio [OR] T C = 1.15, 95% confidence interval [CI] 0.95-1.40, probability of rejection [POR] = 0.014; OR TT CC = 1.32, 95% CI 1.01-1.73, POR = 0.045; OR TC CC = 1.32, 95% CI 0.98-1.21, POR = 0.128; OR TT + TC CC = 1.10, 95% CI 1.00-1.20, POR = 0.05; OR TT CC + TC = 1.26, 95% CI 0.95-1.57, POR = 0.103). Sensitivity analysis confirmed the reliability of these findings. Our study shows that individuals carrying the NQO1 C609T variant allele and genotypes are more susceptible to EC.
许多研究报告称,烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H)醌氧化还原酶1(NQO1)C609T基因多态性会影响食管癌(EC)的发病风险。然而,研究结果仍存在争议且不明确。我们进行了一项荟萃分析,纳入了13项独立研究,共2357名受试者,以检验NQO1 C609T基因多态性与食管癌之间的关联。通过五种不同的基因模型评估这种关联。总体分析表明,变异等位基因和基因型与食管癌风险增加显著相关(优势比[OR]T对C = 1.15,95%置信区间[CI]0.95 - 1.40,拒绝概率[POR] = 0.014;OR TT对CC = 1.32,95% CI 1.01 - 1.73,POR = 0.045;OR TC对CC = 1.32,95% CI 0.98 - 1.21,POR = 0.128;OR TT + TC对CC = 1.10,95% CI 1.00 - 1.20,POR = 0.05;OR TT对CC + TC = 1.26,95% CI 0.95 - 1.57,POR = 0.103)。敏感性分析证实了这些发现的可靠性。我们的研究表明,携带NQO1 C609T变异等位基因和基因型的个体更容易患食管癌。