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东亚人群中髓过氧化物酶463G>A基因多态性与肺癌风险的关联。

The association between myeloperoxidase 463G>A polymorphisms and risk of lung cancer in East-Asia population.

作者信息

Hou Xin, Gao Yuhua, Duan Yongjian, Wang Zhiwei, Shi Lei, Ma Jincheng, Xie Xuanhu

机构信息

Department of Oncology, The First Affiliated Hospital of Henan University, Henan, Kaifeng 475000, PR China.

出版信息

J Cancer Res Ther. 2015 Aug;11 Suppl 1:C97-100. doi: 10.4103/0973-1482.163854.

Abstract

OBJECTIVE

The association between the myeloperoxidase (MPO) 463 G>A polymorphism and lung cancer risk remains controversial. We perform this meta-analysis to further evaluate the MPO 463G>A polymorphism and lung cancer susceptibility.

MATERIALS AND METHODS

We performed the systemic literature search in PubMed, EMBASE, WANFANG, and CNKI databases for molecular epidemiologic studies on the association of MPO 463G>A polymorphism and lung cancer susceptibility. The pooled odds ratio (OR) of MPO 463G>A polymorphism and lung cancer risk were calculated by random or fixed effect model.

RESULTS

Seven case-control studies including 1538 lung cancer patients in the case group and 1673 healthy controls in the control group were included in this study. MPO 463G>A polymorphism was not associated with lung cancer susceptibility under the condition of recessive genetic model (AA vs. GG+GA) (OR = 0.69, P > 0.05) and homozygous genetic model (AA vs. GG) (OR = 0.65, P > 0.05). However, we found significantly decreased risk of lung cancer under dominant genetic model (GA+AA vs. GG) (OR = 0.84, P < 0.05). And no publication bias was found in this meta-analysis for the three genetic models (P > 0.05).

CONCLUSION

This meta-analysis indicated that people with AA genetic type may have decreased lung cancer risk under dominant genetic model.

摘要

目的

髓过氧化物酶(MPO)463G>A多态性与肺癌风险之间的关联仍存在争议。我们进行这项荟萃分析以进一步评估MPO 463G>A多态性与肺癌易感性。

材料与方法

我们在PubMed、EMBASE、万方和知网数据库中进行了系统的文献检索,以查找关于MPO 463G>A多态性与肺癌易感性关联的分子流行病学研究。通过随机或固定效应模型计算MPO 463G>A多态性与肺癌风险的合并比值比(OR)。

结果

本研究纳入了7项病例对照研究,病例组包括1538例肺癌患者,对照组包括1673例健康对照。在隐性遗传模型(AA与GG+GA)(OR = 0.69,P>0.05)和纯合子遗传模型(AA与GG)(OR = 0.65,P>0.05)条件下,MPO 463G>A多态性与肺癌易感性无关。然而,我们发现在显性遗传模型(GA+AA与GG)下肺癌风险显著降低(OR = 0.84,P<0.05)。并且在该荟萃分析中,三种遗传模型均未发现发表偏倚(P>0.05)。

结论

这项荟萃分析表明,在显性遗传模型下,AA基因型的人可能肺癌风险降低。

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