Pathway discovery, validation and compound identification for Alzheimer's disease
Pathway discovery, validation and compound identification for Alzheimer's disease
批准号:
8735842
负责人:
DAVID ALAN BENNETT
金额:
$177.11万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-09-20 至 2018-08-31
关键词:
AdoptedAgingAlzheimer&aposs DiseaseAstrocytesBiologyBrainCandidate Disease GeneClinicalClinical TrialsCohort StudiesCoupledDataData SetDementiaDevelopmentEnsureFDA approvedFailureFoundationsFreezingFunctional disorderGene ComponentsGenerationsGenesGenomicsGoalsHealthHumanImpaired cognitionIndustryInterventionInvestigationInvestmentsKnowledgeLeadMemoryMiningMolecularMolecular TargetNeuronsNodalPathologicPathologyPathway interactionsPharmaceutical PreparationsPhase III Clinical TrialsPlayPredispositionPrefrontal CortexPreventionPrevention approachPrimary PreventionProcessProteinsProteomicsRNA InterferenceRecommendationReligion and SpiritualityResearchRiskRoleSecondary PreventionStagingSting InjurySystems BiologyTechnologyTherapeuticTissue SampleUnited States National Institutes of HealthValidationbrain tissuecell typedrug discoveryepigenomicsflexibilityinduced pluripotent stem cellinterestnetwork modelsnew therapeutic targetnovelnovel strategiesoverexpressionpre-clinicalpreclinical studypreventprimary outcomepublic health prioritiesskillssmall moleculetooltranscriptomicsvalidation studies
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The overall goal of the proposed study is the discovery and preclinical validation of novel targets associated with molecular processes that lead to cognitive decline, the primary outcome of most AD trials. The recent NIA Alzheimer's Disease Research Summit 2012: Path to Treatment and Prevention that led to the RFA to which we are responding, made a number of recommendations which motivated the strategy adopted in the proposed study. Our proposal brings together an exceptionally strong and unique multi-disciplinary team with the relevant skills needed to achieve our overall goal. In Aim 1, we take a systems biology approach to mine a truly unique set of deep clinical, paraclinical, pathologic, genomic, epigenomic, and transcriptomic data assembled from frozen dorsolateral prefrontal cortex brain tissue of 1000 subjects from two cohort studies of aging and dementia, the Religious Order Study and the Memory and Aging Project, in conjunction with other publicly available functional datasets. These unique data provide an excellent substrate for the identification and nomination of molecular targets for drug discovery. Target discovery is coupled with a flexible translational strategy that first validates targets by a targeted proteomic study of brain tissue from the same region and subjects in Aim 2. In Aim 3, an RNA interference (RNAi) and overexpression functional validation study in cultured human neurons and astrocytes is executed in parallel in Aim 3. Finally, these data come together in Aim 4 which performs high throughput small molecule screens on neurons and astrocytes derived from induced pluripotent stem cells (iPSC) on the most promising targets. Our proposal is ambitious but realistic: it reflects the deployment of cutting-edge approaches with a practical mindset in which redundancies have been carefully considered to mitigate risk and ensure the delivery of data, network models and lead compounds. The proposed study will discover and validate novel targets associated with molecular processes that lead to cognitive decline, and it will demonstrate the druggability of one or more targets, setting the stage for clinical trials with new
and novel approaches to the prevention and treatment of AD.
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海外基金