Role of Nicotine in Lung Carcinogenesis
Role of Nicotine in Lung Carcinogenesis
批准号:
8081040
负责人:
CHANGYAN CHEN
金额:
$27.21万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-15 至 2013-04-17
关键词:
AffectApoptosisApoptoticBindingBiochemicalBiologicalBlood CirculationBrainCancer EtiologyCancer PatientCarcinogensCell Cycle CheckpointCell Cycle ProgressionCell ProliferationCholinergic ReceptorsCigaretteCyclin D1DataDevelopmentDrosophila acetylcholine receptor alpha-subunitEnhancersEnvironmentEnvironmental Tobacco SmokeEpithelialEpithelial CellsEventExposure toG CellsGrowthHumanLungMalignant NeoplasmsMalignant neoplasm of lungMediatingMitogensMolecularMolecular TargetMusNeurogliaNicotineNicotine DependencePathway interactionsPatientsPhosphorylationPhosphotransferasesPlayProtein Kinase CRadiation therapyRas Signaling PathwayRattusResearch PersonnelResistanceRoleSignal PathwaySignal TransductionSmokerSurfaceSynaptic TransmissionTestingTherapeutic UsesTobaccoTobacco useUp-RegulationVascular Endothelial Cellbasecancer cellcell growthcell typechronic paincigarette smokingcigarette smokingcyclin Gin vivoinsightlung cancer preventionlung carcinogenesislung tumorigenesisnoveloverexpressionprogramsras Proteinsreceptorresearch studyresponsesmoking cessationtumorigenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Cigarette smoking is strongly correlated with onset of lung cancer and statistically more than 90% of lung cancer patients are smokers. However, lung cancer caused by second-hand smoking remains unknown. Nicotine is a major component of cigarettes and exists at high concentrations in the bloodstream of smokers. Nicotine-based products are widely used to aid smoking cessation and to treat patients clinically with chronic pain. Studies have shown that nicotine binds to nicotine acetylcholine receptors (nAChRs) and further activates several mitogen-related signaling pathways in various types of cells including lung epithelial and cancer cells and vascular endothelial cells. The anti-apoptotic activity of Bcl-2 is also induced by nicotine treatment. We demonstrated that nicotine activates Ras and protein kinase C (PKC) pathways, leading to the disruption of cell growth restriction. However, the mechanisms of nicotine in the onset or development of lung cancer remain to be elucidated. Therefore, our long-term objective of the proposal is to study the role of nicotine in lung carcinogenesis. Such study will identify novel components in nicotine-mediated signaling pathways and will help modifying the current usage of nicotine. The central hypothesis of the proposal is that nicotine acts as a potential carcinogen that can mobilize intracellular growth-related signal pathways and antagonize apoptotic signaling, which creates a permissive environment for tumorigenesis. The specific aims to test the hypothesis are: 1) to investigate the mechanisms of nicotine-mediated cell growth promotion; 2) to determine how nicotine exposure perturbs G1 cell cycle checkpoint; 3) to study the molecular mechanisms of nicotine-mediated anti-apoptotic action. Mouse or rat lung epithelial and various human lung cancer cells will be used in the proposed experiments. Our understanding of nicotine will not only offer a cautionary stance for the therapeutic use of this compound, but also help developing new stratigies for treating nicotine addiction or chronic pain cessation.
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Study of Ras-Mediated Apoptosis
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资助金额:$26.44万
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财政年份:2004
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依托单位:
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批准号:6826031
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项目类别:
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资助金额:$25.23万
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依托单位:
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批准号:6913618
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负责人:CHANGYAN CHEN
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项目类别:
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资助金额:$25.86万
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负责人:CHANGYAN CHEN
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依托单位:
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批准号:9257294
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项目类别:
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资助金额:$24.18万
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财政年份:2004
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负责人:CHANGYAN CHEN
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依托单位:
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