Verde Zoraida, Reinoso Luis, Chicharro Luis Miguel, Resano Pilar, Sánchez-Hernández Ignacio, Rodríguez González-Moro Jose Miguel, Bandrés Fernando, Gómez-Gallego Félix, Santiago Catalina
Department of Morphological Sciences and Biomedicine, Universidad Europea, Madrid, Spain.
Department of Morphological Sciences and Biomedicine, Universidad Europea, Madrid, Spain; Department of Occupational Health, Grupo Banco Popular, Madrid, Spain.
PLoS One. 2015 May 27;10(5):e0129374. doi: 10.1371/journal.pone.0129374. eCollection 2015.
Variations in tobacco-related cancers, incidence and prevalence reflect differences in tobacco consumption in addition to genetic factors. Besides, genes related to lung cancer risk could be related to smoking behavior. Polymorphisms altering DNA repair capacity may lead to synergistic effects with tobacco carcinogen-induced lung cancer risk. Common problems in genetic association studies, such as presence of gene-by-environment (G x E) correlation in the population, may reduce the validity of these designs. The main purpose of this study was to evaluate the independence assumption for selected SNPs and smoking behaviour in a cohort of 320 healthy Spanish smokers. We found an association between the wild type alleles of XRCC3 Thr241Met or KLC3 Lys751Gln and greater smoking intensity (OR = 12.98, 95% CI = 2.86-58.82 and OR=16.90, 95% CI=2.09-142.8; respectively). Although preliminary, the results of our study provide evidence that genetic variations in DNA-repair genes may influence both smoking habits and the development of lung cancer. Population-specific G x E studies should be carried out when genetic and environmental factors interact to cause the disease.
除遗传因素外,烟草相关癌症的发病率和患病率差异反映了烟草消费的差异。此外,与肺癌风险相关的基因可能与吸烟行为有关。改变DNA修复能力的多态性可能会与烟草致癌物诱发的肺癌风险产生协同效应。遗传关联研究中的常见问题,如人群中基因-环境(G×E)相关性的存在,可能会降低这些设计的有效性。本研究的主要目的是评估320名健康西班牙吸烟者队列中所选单核苷酸多态性(SNP)与吸烟行为的独立性假设。我们发现XRCC3 Thr241Met或KLC3 Lys751Gln的野生型等位基因与更高的吸烟强度之间存在关联(比值比分别为12.98,95%置信区间为2.86 - 58.82;以及比值比为16.90,95%置信区间为2.09 - 142.8)。尽管是初步的,但我们的研究结果提供了证据表明DNA修复基因的遗传变异可能会影响吸烟习惯和肺癌的发生。当遗传和环境因素相互作用导致疾病时,应开展针对特定人群的基因-环境研究。