Genetic Susceptibility to Lung Cancer

肺癌的遗传易感性

• 批准号: 7236616
• 负责人: David C Christiani
• 金额: $ 67.5万
• 依托单位: HARVARD SCHOOL OF PUBLIC HEALTH
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-04-10 至 2009-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7236616
• 关键词: Address; Affect; Age; Alleles; Antioxidants; Ascorbic Acid; Bronchogenic Carcinoma; Cancer Etiology; Carcinogens; Carotenoids; Case-Control Studies; Cell Respiration; Characteristics; Cigarette; Codon Nucleotides; DNA Repair; DNA Repair Gene; Defect; Development; Diet; Diet Modification; Dietary intake; Dose; Drug Metabolic Detoxication; EPHX1 gene; ERCC2 gene; Environment; Environmental Risk Factor; Enzymes; Family; GSTP1 gene; GSTT1 gene; GSTT1 protein; Gender; Gender Role; Gene Mutation; Genes; Genetic; Genetic Polymorphism; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutathione S-Transferase; Growth Factor; High Risk Woman; Histologic; Hospitals; Human; Individual; Inflammatory; Inherited; Integration Host Factors; Interstitial Collagenase; Lead; Literature; Lung; Malignant neoplasm of lung; Manganese Superoxide Dismutase; Matrix Metalloproteinases; Meat; Metabolic; Metabolism; Metalloproteinase Gene; Minority; Modification; Molecular Epidemiology; NAT2 gene; National Cancer Institute; Numbers; Oncogenes; Pathway interactions; Peroxidase; Phase; Population; Predisposition; Prevention strategy; Process; Property; Reactive Oxygen Species; Research; Risk; Role; Sample Size; Smoke; Smoker; Smoking; Specificity; TP53 gene; Tobacco; Tobacco smoke; Tumor Cell Invasion; Tumor Suppression; Tumor Suppressor Genes; Tumor Suppressor Proteins; United States; Variant; Woman; XRCC1 gene; Xenobiotic Metabolism; Xenobiotics; arginylproline; base; cancer risk; cell type; cigarette smoking; cruciferous vegetable; fruits and vegetables; gene interaction; glutathione S-transferase pi; glutathione peroxidase GPX1; improved; men; mortality; tumor

DESCRIPTION (provided by applicant): Lung cancer is the most common cause of cancer mortality among both men and women in the United States. Although up to 90 percent of lung cancer is attributable to cigarette smoking, only 10-20 percent of smokers develop bronchogenic carcinoma over their lifetimes. This observation, along with substantial literature implicating heritable polymorphic factors, indicates that other environmental and host factors influence individual susceptibility to tobacco smoke. This proposal will take advantage of recent advances in molecular epidemiology in this competing continuation (R01 CA 74386) by expanding our original aims of evaluating six xenobiotic metabolic polymorphisms in lung cancer to include the assessment of more recently described polymorphic genes that control oxidative metabolism (Phase I) and the conjugation of reactive intermediates (Phase II). In addition, a number of other polymorphic genes that affect lung inflammatory processes, DNA repair, growth factor function, and tumor suppression (oncogenes) will be evaluated, as there is accumulating evidence supporting the role of these non-metabolism polymorphic alleles in lung cancer development. Moreover, this proposal addresses the role of smoking, diet, and genetic factors as effect modifiers for the association between polymorphisms and lung cancer risk, and the potential roles of age and gender in these associations. To assess these gene-environment and gene gene associations in this expanded group of polymorphic genes, our proposal will build on our productive R01 by increasing our sample size and including greater population diversity by increasing minority recruitment. A better understanding of these risks will lead to improved preventive strategies. The proposal directly addresses two "Extraordinary Opportunities" of the National Cancer Institute, specifically the aim to identify genetic variations that affect cancer risk in concert with environmental factors, and research on tobacco-related concerns.

描述（由申请人提供）：肺癌是美国男性和女性癌症死亡的最常见原因。尽管高达90%的肺癌可归因于吸烟，但只有10- 20%的吸烟者在一生中患上支气管癌。这一观察结果，沿着大量文献暗示遗传多态性因素，表明其他环境和宿主因素影响个体对烟草烟雾的易感性。这项建议将利用分子流行病学的最新进展，在这一竞争的延续（R 01 CA 74386），扩大我们原来的目标，评估六个外源性代谢多态性肺癌，包括评估最近描述的多态性基因，控制氧化代谢（第一阶段）和共轭反应中间体（第二阶段）。此外，还将评估影响肺部炎症过程、DNA修复、生长因子功能和肿瘤抑制（癌基因）的许多其他多态性基因，因为有越来越多的证据支持这些非代谢多态性等位基因在肺癌发生中的作用。此外，该提案还讨论了吸烟、饮食和遗传因素作为多态性与肺癌风险之间关联的效应调节剂的作用，以及年龄和性别在这些关联中的潜在作用。为了评估这些基因-环境和基因在这个扩大的多态性基因组中的基因关联，我们的建议将建立在我们的生产R 01的基础上，通过增加我们的样本量，并通过增加少数民族的招募来增加人口多样性。更好地了解这些风险将有助于改进预防战略。该提案直接涉及国家癌症研究所的两个“非常机会”，具体而言，旨在确定与环境因素一起影响癌症风险的遗传变异，以及对烟草相关问题的研究。