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Tobacco consumption, genetic susceptibility, gene-environment interaction and lung cancer risk.

机译:烟草消费,遗传易感性,基因-环境相互作用和肺癌风险。

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摘要

Introduction. Lung cancer is the most common cancer and the leading cause of cancer death worldwide. Tobacco smoking has been established as the most important etiological factor of lung cancer for both men and women. However only a fraction of the smokers will eventually develop lung cancer, depending on the extent of smoking, exposure to other environmental carcinogens and individual susceptibility. To elucidate the etiological mechanism of lung carcinogenesis, and identify high-risk individuals for disease prevention and control, we studied host susceptibility and its interactions with environmental factors on the risk of lung cancer.;Methods. There are three parts in this dissertation. First, to evaluate the effects of different tobacco consumption habits (smoking, chewing) on lung cancer risks, data from a hospital-based case-control study from southern India comprised of 778 male lung cancer cases and 3430 male controls were analyzed. Second, to assess the relationship between genetic variations and lung cancer risks, and their possible gene-gene and gene-environmental interactions, genetic polymorphisms were assayed in a multicenter case-control study in Eastern Europe that included 2188 lung cancer cases and 2198 hospital controls. Third, to demonstrate the application of hierarchical modeling, a case-control study of bladder cancer was used.;Results. Bidi smoking was found to be at least equally carcinogenic as cigarette smoking. Genetic polymorphisms may influence individual susceptibility to lung cancer. The magnitude of the effect is modulated by levels and types of exposures to carcinogens. The effect of genetic polymorphism is often moderate. However, when considering multiple genes simultaneously, number of prior risk alleles is associated with a significant increase of lung cancer risk. Moreover, the combination of certain occupational exposures and risk genotypes may increase lung cancer risk to a considerable extent. Hierarchical modeling may improve the estimation by increased precision and incorporating prior knowledge.;Significance. The results of this proposed study may offer a more complete picture of the association of lung cancer risk with tobacco consumption, genetic susceptibility and gene-environmental interaction. The findings of the study will help to clarify etiological mechanisms of lung cancer development for effective cancer prevention and control.
机译:介绍。肺癌是全球最常见的癌症,也是导致癌症死亡的主要原因。吸烟已被确定为男性和女性肺癌的最重要病因。但是,根据吸烟程度,暴露于其他环境致癌物和个人易感性,只有一小部分吸烟者最终会患上肺癌。为了阐明肺癌致癌的病因机制,并确定高危人群进行疾病预防和控制,我们研究了宿主易感性及其与环境因素的相互作用对肺癌风险的影响。本文共分三个部分。首先,为评估不同吸烟习惯(吸烟,咀嚼)对肺癌风险的影响,分析了来自印度南部的一项基于医院的病例对照研究的数据,该研究包括778例男性肺癌病例和3430例男性对照。其次,为了评估遗传变异与肺癌风险及其可能的基因-基因和基因-环境相互作用之间的关系,在东欧的一项多中心病例对照研究中分析了遗传多态性,其中包括2188例肺癌病例和2198例医院对照。第三,为了证明分层建模的应用,对膀胱癌进行了病例对照研究。人们发现,比迪吸烟与吸烟至少具有相同的致癌性。遗传多态性可能会影响个体对肺癌的敏感性。影响的程度受致癌物暴露的水平和类型的调节。遗传多态性的影响通常是中等的。然而,当同时考虑多个基因时,先验风险等位基因的数量与肺癌风险的显着增加相关。而且,某些职业暴露和危险基因型的组合可能在很大程度上增加肺癌的风险。层次建模可以通过提高精度和合并先验知识来改进估计。这项拟议研究的结果可能为肺癌风险与烟草消费,遗传易感性和基因-环境相互作用之间的联系提供更完整的描述。该研究结果将有助于阐明肺癌发展的病因机制,以有效地预防和控制癌症。

著录项

  • 作者

    Hung, Rayjean Jui-chun.;

  • 作者单位

    University of California, Los Angeles.;

  • 授予单位 University of California, Los Angeles.;
  • 学科 Public health.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 253 p.
  • 总页数 253
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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