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基因中G134A和G184C多态性与肺癌发病率的关联。

Association of the G134A and G184C Polymorphisms in the Gene with Lung Cancer Incidence.

作者信息

Ryu Doug-Young, Huang Mingai, Park Changbo, Chang Soo Im, Im Ruth, Choi Seong-Jin, Kim Na-Young, Park In Won, Choi Byoung Whui, Kim Jae Yeol, Shin Jong Wook, Choi Jae Chul, Choi Byung-Sun, Park Jung-Duck

机构信息

13College of Veterinary Medicine, Seoul National University, Seoul, 151-742 Korea.

23College of Medicine, Chung-Ang University, Seoul, 156-756 Korea.

出版信息

Toxicol Res. 2008 Jun;24(2):109-112. doi: 10.5487/TR.2008.24.2.109. Epub 2008 Jun 1.

Abstract

The G184C and G134A single nucleotide polymorphisms (SNPs) of the gene result in Ala62Pro and Gly45Asp substitutions, respectively. Here, we tested whether these SNPs are associated with an alteration in lung cancer incidence. We examined 80 Korean subjects with lung cancer and 240 age- and sex-matched controls. For each subject, the gene was PCR amplified and sequenced. We observed that the odds ratio (OR) for lung cancer was 3.37 higher in subjects with the G184C polymorphism than in controls (95% confidence interval (CI), 0.8912.73, = 0.07). In contrast, the OR for lung cancer was 1.23 in subjects with the G134A polymorphism compared to controls (95% CI, 0.682.20, = 0.49). The G184C polymorphism exacerbated the effects of smoking on lung cancer development. Gene-smoking interaction analyses revealed that past or present smokers with the G184C polymorphism had a higher incidence of lung cancer (OR, 24.72; 95% CI, 4.48136.31; < 0.01) than control smokers (OR, 6.65; 95% CI, 2.7216.28; < 0.01). However, there was only a slight difference in the ORs for lung cancer between control smokers and smokers with the G134A polymorphism. These findings suggest that the G184C polymorphism, but not the G134A polymorphism, is associated with an increased risk of lung cancer.

摘要

该基因的G184C和G134A单核苷酸多态性(SNP)分别导致Ala62Pro和Gly45Asp替代。在此,我们测试了这些SNP是否与肺癌发病率的改变相关。我们检查了80名韩国肺癌患者和240名年龄及性别匹配的对照。对每个受试者,该基因进行PCR扩增并测序。我们观察到,具有G184C多态性的受试者患肺癌的优势比(OR)比对照组高3.37(95%置信区间(CI),0.8912.73,P = 0.07)。相比之下,具有G134A多态性的受试者患肺癌的OR为1.23(95% CI,0.682.20,P = 0.49)。G184C多态性加剧了吸烟对肺癌发生的影响。基因-吸烟相互作用分析显示,具有G184C多态性的既往或当前吸烟者患肺癌的发病率(OR,24.72;95% CI,4.48136.31;P < 0.01)高于对照吸烟者(OR,6.65;95% CI,2.7216.28;P < 0.01)。然而,对照吸烟者和具有G134A多态性的吸烟者之间患肺癌的ORs仅有轻微差异。这些发现表明,G184C多态性而非G134A多态性与肺癌风险增加相关。

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