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MPO、GSTT1、GSTM1、GSTP1、EPHX1 和 NQO1 基因多态性与早发性肺癌的风险因素。

Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early-onset lung cancer.

机构信息

Department of Epigenomics and Cancer Risk Factors, German Cancer Research Centre (DKFZ), Heidelberg, Germany.

出版信息

Int J Cancer. 2010 Oct 1;127(7):1547-61. doi: 10.1002/ijc.25175.

Abstract

Early-onset lung cancer diagnosed up to the age of 50 is a very rare disease, with an increasing incidence rate. Differences in aetiology, characteristics and epidemiology of early and older onset lung cancer have been described previously, suggesting the importance of genetic factors in early-onset lung cancer aetiology. A case-control study was conducted to investigate the effects of genetic polymorphisms in the MPO, EPHX1, GSTT1, GSTM1, GSTP1 and NQO1 genes on the risk of early-onset lung cancer development. Six hundred thirty-eight Caucasian patients under the age of 51 with confirmed primary lung cancer and 1,300 cancer free control individuals, matched by age and sex, were included in this analysis. Seventeen single nucleotide polymorphisms and two deletion polymorphisms were genotyped. No significant association was found for any of the analyzed polymorphisms and overall lung cancer risk. Nonsignificantly decreased risk of lung cancer was observed for carriers of 1 or 2 copies of GSTM1. Subgroup analysis revealed gender- and/or smoking-specific effects of EPHX1 rs2854455 (IV-1464C > T) and rs2234922 (His139Arg), GSTT1 deletion, GSTP1 rs1695 (Ile105Val), rs947895 (+991C > A) and rs4891 (Ser185Ser) and NQO1 rs1800566 (Pro187Ser) polymorphisms. However, none of the observed effects were confirmed by interaction tests nor were they significant after Bonferroni correction for multiple testing. In summary, our study suggested a modifying effect of polymorphisms in EPHX1, GSTP1, GSTT1, GSTM1 and NQO1 genes on the risk of early-onset lung cancer. To confirm these observations and to eliminate possible bias in our analyses, larger studies are warranted.

摘要

早发性肺癌是一种非常罕见的疾病,发病年龄在 50 岁以下,发病率呈上升趋势。之前已经描述了早发性和老年发病肺癌的病因、特征和流行病学差异,这表明遗传因素在早发性肺癌的发病机制中起重要作用。本研究采用病例对照研究,旨在探讨 MPO、EPHX1、GSTT1、GSTM1、GSTP1 和 NQO1 基因的遗传多态性对早发性肺癌发病风险的影响。该研究共纳入 638 名年龄在 51 岁以下确诊为原发性肺癌的高加索裔患者和 1300 名年龄和性别匹配的无癌对照个体,分析了 17 个单核苷酸多态性和 2 个缺失多态性。未发现任何分析的多态性与总体肺癌风险相关。携带 1 或 2 个 GSTM1 拷贝的个体患肺癌的风险略有降低。亚组分析显示,EPHX1 rs2854455(IV-1464C > T)和 rs2234922(His139Arg)、GSTT1 缺失、GSTP1 rs1695(Ile105Val)、rs947895(+991C > A)和 rs4891(Ser185Ser)以及 NQO1 rs1800566(Pro187Ser)多态性与性别和/或吸烟有关。然而,经交互检验和多重检验校正后,这些效应均未得到证实。综上所述,本研究提示 EPHX1、GSTP1、GSTT1、GSTM1 和 NQO1 基因的多态性对早发性肺癌的发病风险有修饰作用。为了证实这些观察结果并消除我们分析中的可能偏差,需要进行更大规模的研究。

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