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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Lung cancer susceptibility and genetic polymorphisms of Exo1 gene in Taiwan.
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Lung cancer susceptibility and genetic polymorphisms of Exo1 gene in Taiwan.

机译:台湾地区Exo1基因的肺癌易感性和遗传多态性。

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摘要

AIM: To evaluate the association between the polymorphisms of the Exo1 gene and the risk of lung cancer in central Taiwan. PATIENTS AND METHODS: In this hospital-based study, the association of Exol A-1419G (rs3754093), C-908G (rs10802996), A238G (rs1776177), C498T (rs1635517), K589E (rs1047840), G670E (rs1776148), C723R (rs1635498), L757P (rs9350) and C3114T (rs851797) polymorphisms with lung cancer risk in a central Taiwanese population was investigated. In total, 358 patients with lung cancer and 358 age- and gender-matched healthy controls recruited from the China Medical Hospital in central Taiwan were genotyped. RESULTS: A significantly different distribution was found in the frequency of the Exo1 K589E genotype, but not the other genotypes, between the lung cancer and control groups. The A allele Exo1 K589E conferred a significantly (p = 0.0097) increased risk of lung cancer. As for the rest of the polymorphisms, there was no difference in distribution between the lung cancer and control groups. Gene environment interactions with smoking were significant for Exo1 K589E polymorphism. The Exo1 K589E AG and AA genotype in association with smoking conferred an increased risk of 1.7208 (95% confidence interval = 1.2188-2.4295) for lung cancer. CONCLUSION: Our results provide the first evidence that the A allele of Exo1 K589E may be associated with the development of lung cancer and may be a novel useful marker for primary prevention and anticancer intervention.
机译:目的:评估台湾中部地区Exo1基因多态性与肺癌风险之间的关系。患者和方法:在这项基于医院的研究中,Exol A-1419G(rs3754093),C-908G(rs10802996),A238G(rs1776177),C498T(rs1635517),K589E(rs1047840),G670E(rs1776148),C723R (rs1635498),L757P(rs9350)和C3114T(rs851797)多态性在台湾中部人群中有肺癌风险。从台湾中部中华医院招募的358名肺癌患者和358名年龄和性别相匹配的健康对照者进行了基因分型。结果:在肺癌和对照组之间,Exo1 K589E基因型的频率存在显着不同的分布,而其他基因型则没有。 A等位基因Exo1 K589E显着增加(p = 0.0097)患肺癌的风险。至于其余的多态性,肺癌与对照组之间的分布没有差异。基因环境与吸烟的相互作用对于Exo1 K589E多态性具有重要意义。 Exo1 K589E AG和AA基因型与吸烟相关,使肺癌的风险增加了1.7208(95%置信区间= 1.2188-2.4295)。结论:我们的结果提供了第一个证据,证明Exo1 K589E的A等位基因可能与肺癌的发展有关,并且可能是一级预防和抗癌干预的新型有用标记。

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