The relationship between three well-characterized polymorphisms of the angiotensin converting enzyme gene and lung cancer risk: a case-control study and a meta-analysis.

IF 4.1
Min Gao, Yuli Wang, Yuzhi Shi, Dan Liu, Yin Liang, Yan Yu, Jiahui Zhaobin, Lili Zhu, Shoude Jin
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引用次数: 22

Abstract

Background and objective: The gene encoding angiotensin converting enzyme (ACE) is a promising candidate for lung cancer. We aimed to assess three well-characterized polymorphisms of the ACE gene (A-240T, I/D, A2350G) and lung cancer in Chinese people, and complete a meta-analysis of the association of I/D polymorphism with lung cancer.

Methods and results: In our case-control study, a total of 684 patients with lung cancer and 602 age-matched controls were recruited. Genotyping was performed using polymerase chain reaction (PCR) and ligase detection reactions (LDR) techniques. Single-locus analysis indicated that carriers of the A-240T allele had a significantly increased risk for lung cancer under additive (odds ratio (OR)=1.2; 95% confidence interval (CI): 1.02-1.42; P=0.027) and recessive (OR=1.8; 95% CI: 1.24-2.63; P=0.002) models, and that DD genotype carriers were 1.97 times more likely to develop lung cancer (95% CI: 1.25-3.11; P=0.004) compared with those with the I allele under the recessive model. However, no significance was observed in further haplotype analysis (P>0.05). In a meta-analysis of ACE gene insertion-deletion (I/D) polymorphism from six studies with 1183 lung cancer patients and 1065 controls, we failed to detect any significant association (overall OR=1.09; 95% CI: 0.84-1.41). A low probability of publication bias was observed.

Conclusions: Our results suggest that ACE gene A-240T polymorphism might be a genetic marker for the development of lung cancer in Chinese people.

血管紧张素转换酶基因的三种明显多态性与肺癌风险之间的关系:一项病例对照研究和荟萃分析。
背景与目的:血管紧张素转换酶(ACE)编码基因是肺癌的一个有希望的候选基因。我们旨在评估ACE基因(a- 240t, I/D, A2350G)与中国人肺癌的三种明显多态性,并完成I/D多态性与肺癌相关性的荟萃分析。方法与结果:在我们的病例对照研究中,共招募了684例肺癌患者和602例年龄匹配的对照组。采用聚合酶链反应(PCR)和连接酶检测反应(LDR)技术进行基因分型。单位点分析表明,a - 240t等位基因携带者在加性条件下患肺癌的风险显著增加(优势比(OR)=1.2;95%置信区间(CI): 1.02-1.42;P=0.027)和隐性(OR=1.8;95% ci: 1.24-2.63;P=0.002)模型,DD基因型携带者患肺癌的可能性是后者的1.97倍(95% CI: 1.25-3.11;P=0.004)。单倍型分析无显著性差异(P>0.05)。在一项来自6项研究(1183名肺癌患者和1065名对照)的ACE基因插入-缺失(I/D)多态性荟萃分析中,我们未能发现任何显著关联(总OR=1.09;95% ci: 0.84-1.41)。发表偏倚的概率较低。结论:ACE基因a - 240t多态性可能是中国人肺癌发生的遗传标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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