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烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H):奎宁氧化还原酶1(NQO1)基因609 C>T多态性与胃癌风险相关:一项病例对照研究和荟萃分析的证据。

The NAD(P)H: quinine oxidoreductase 1 (NQO1) gene 609 C>T polymorphism is associated with gastric cancer risk: evidence from a case-control study and a meta-analysis.

作者信息

Hu Wei-Guo, Hu Jia-Jia, Cai Wei, Zheng Min-Hua, Zang Lu, Wang Zheng-Ting, Zhu Zheng-Gang

机构信息

Department of General Surgery, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China E-mail :

出版信息

Asian Pac J Cancer Prev. 2014;15(5):2363-7. doi: 10.7314/apjcp.2014.15.5.2363.

DOI:10.7314/apjcp.2014.15.5.2363
PMID:24716985
Abstract

UNLABELLED

The association between the

NAD(P)H: quinone oxidoreductase 1 (NQO1) gene C609T polymorphism (rs1800566) and gastric cancer has been widely evaluated, but a definitive answer is so far lacking. We first conducted a case-control study to assess this association in a large Han Chinese population, and then performed a meta-analysis to further address this issue. Although our case-control association study indicated no significant difference in the genotype and allele distributions of C609T polymorphism between gastric cancer patients and controls, in the meta analysis involving 4,000 subjects, comparison of alleles 609T and 609C indicated a significantly increased risk (46%) for gastric cancer (95% confidence interval (95%CI) for odds ratio (OR)=1.20- 1.79) in individuals with the T allele. The tendency was similar to the homozygote (OR=1.81, 95%CI: 1.16-2.84), dominant models (OR=1.41, 95%CI: 1.12-1.79), as well as recessive model (OR=1.58, 95%CI: 1.06-2.35). Stratified analysis by study design demonstrated stronger associations in population-based than in hospital-based studies. And ethnicity-based analysis demonstrated a significant association in Asians. We conclude that the NQO1 gene C609T polymorphism increases the risk for gastric cancer, especially in Asian populations.

摘要

未标注

烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H):醌氧化还原酶1(NQO1)基因C609T多态性(rs1800566)与胃癌之间的关联已得到广泛评估,但目前仍缺乏明确答案。我们首先进行了一项病例对照研究,以评估这种关联在一大群中国汉族人群中的情况,然后进行了一项荟萃分析以进一步探讨这个问题。尽管我们的病例对照关联研究表明,胃癌患者与对照组之间C609T多态性的基因型和等位基因分布没有显著差异,但在涉及4000名受试者的荟萃分析中,等位基因609T与609C的比较表明,携带T等位基因的个体患胃癌的风险显著增加(46%)(优势比(OR)的95%置信区间(95%CI)=1.2 ~ 1.79)。这种趋势在纯合子(OR = 1.81,95%CI:1.16 ~ 2.84)、显性模型(OR = 1.41,95%CI:1.12 ~ 1.79)以及隐性模型(OR = 1.58,95%CI:1.06 ~ 2.35)中相似。按研究设计进行的分层分析表明,基于人群的研究比基于医院的研究关联更强。基于种族的分析表明,在亚洲人群中存在显著关联。我们得出结论,NQO1基因C609T多态性会增加患胃癌的风险,尤其是在亚洲人群中。

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