课题基金 / 基金详情

Matrix Metalloproteinase Gene Polymorphisms and Breast Cancer Risk and Sruvival

Matrix Metalloproteinase Gene Polymorphisms and Breast Cancer Risk and Sruvival
基质金属蛋白酶基因多态性与乳腺癌风险和生存
批准号:
7895897
负责人:
NEERAJA BOYAPATI PETERSON
金额:
$13.08万
依托单位:
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:
2007-08-01 至 2011-07-31
关键词:
AffectAgeApplications GrantsAwardBasement membraneBehavior ControlBenignBreast Cancer Risk FactorBreast CarcinomaBreast DiseasesCancer BiologyCancer EtiologyCellular biologyCessation of lifeChildhoodClinical MedicineComplementCountryDataDetectionDevelopmentDietDiseaseDisease ProgressionElementsEpidemiologic StudiesEventExogenous Hormone TherapyExtracellular MatrixExtracellular Matrix DegradationFamilyFamily history ofFoundationsGelatinase AGelatinase BGeneticGenetic DeterminismGenetic PolymorphismGenetic VariationGenotypeGeographic LocationsHealth Services ResearchHumanHuman GeneticsIn SituIncidenceIndividualInterstitial CollagenaseInvestigationIonizing radiationK-Series Research Career ProgramsKnowledgeLife StyleMalignant NeoplasmsMammographic DensityMatrilysinMatrix MetalloproteinasesMentorsMentorshipMetalloproteinase GeneMolecular EpidemiologyMolecular Epidemiology of CancerMolecular GeneticsNeoplasm MetastasisObesityOutcomePathway interactionsPeptide HydrolasesPhysical activityPlayPopulation SciencesPredispositionRecording of previous eventsResearchResearch ActivityResearch PersonnelResearch SupportResearch TrainingResourcesRiskRisk FactorsRoleScreening procedureSerumStage at DiagnosisStromelysin 1TrainingTraining ProgramsWomanWorkZincanticancer researchbasecancer diagnosiscancer epidemiologycancer preventioncancer riskcancer typecase controlcost effectivenessenzyme activityexperiencegenetic analysisgenetic epidemiologylifestyle factorsmalignant breast neoplasmmortalitynoveloutcome forecastprogramspromoterreproductiveskillstumortumor progression

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中文摘要
翻译
描述(由申请人提供):在这个癌症预防,控制,行为和人口科学职业发展奖(K 07)中提出的重点教学培训,指导和研究将使候选人成为癌症预防的成功,独立的研究者,重点是乳腺癌风险和预后的遗传决定因素。在研究部分,候选人将研究基质金属蛋白酶(MMPs)在乳腺癌中的作用。人MMP家族由超过20种蛋白水解酶组成,其降解细胞外基质的大多数组分,并且与癌症进展密切相关。最近和越来越多的证据表明,MMPs也参与了肿瘤的最初发展。某些MMP基因启动子中的多态性改变了组成型或诱导型表达和酶活性,可能会影响个体对疾病的易感性和/或疾病进展的风险。为了进一步探讨这些关系,本研究的目的是:1)检测MMP基因多态性对乳腺癌风险的贡献; 2)确定MMP基因多态性是否与乳腺癌类型相关(原位vs.侵入性)或诊断时的疾病分期;研究MMP基因多态性与乳腺癌患者全因生存率和乳腺癌特异性生存率的关系。拟议的分析将基于具有里程碑意义的乳腺癌合作研究,这是乳腺癌最大的流行病学研究之一。这项研究的优势包括大量的乳腺癌病例和对照,以及利用现有资源的成本效益。在癌症生物学,人类遗传学和遗传分析,以及分子流行病学的教学培训将填补候选人目前的培训和研究计划的空白。具有癌症和分子流行病学,细胞生物学(专注于MMPs)和人类遗传学专业知识的导师将在整个颁奖期间支持候选人。教学培训和指导研究活动将为她提供研究乳腺癌风险和预后的遗传决定因素的机会,并为她在该奖项的最后几年提交极具竞争力的赠款申请提供基础。
英文摘要
DESCRIPTION (provided by applicant): The focused didactic training, mentorship, and research proposed in this Cancer Prevention, Control, Behavioral, and Population Sciences Career Development Award (K07) will allow the candidate to become a successful, independent investigator in cancer prevention, with a focus on genetic determinants of breast cancer risk and prognosis. In the research component, the candidate will investigate the role of matrix metalloproteinases (MMPs) in breast cancer. The human MMP family consists of over 20 proteolytic enzymes that degrade most components of the extracellular matrix and has been strongly implicated in cancer progression. Recent and growing evidence suggests that MMPs are also involved in the initial development of a tumor. Polymorphisms in certain MMP gene promoters that alter constitutive or induced expression and enzyme activity may affect individual susceptibility to disease and/or risk of disease progression. In order to further explore these relationships, the research aims of this proposal are 1) to examine the contribution of polymorphisms in MMP genes to the risk for breast cancer; 2) to determine if MMP genetic polymorphisms are associated with breast cancer type (in-situ vs. invasive) or disease stage at diagnosis; and 3) to investigate associations of MMP genetic polymorphisms with all-cause survival and breast cancer-specific survival. The proposed analyses will be based on the landmark Collaborative Breast Cancer Study, one of the largest epidemiologic studies in breast cancer. Advantages of this study include the large number of breast cancer cases and controls and the cost-effectiveness of utilizing existing resources. The didactic training in cancer biology, human genetics and genetic analysis, and molecular epidemiology proposed will fill gaps in the candidate's current training and research program. Mentors with expertise in cancer and molecular epidemiology, cell biology with a focus on MMPs, and human genetics will support the candidate throughout the award period. The didactic training and mentored research activities will provide her with opportunities to study genetic determinants of breast cancer risk and prognosis, and provide the foundation for which she can submit highly competitive grant applications in the final years of the award.
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