grant

Program 03 Prostate Cancer

Organization DANA-FARBER CANCER INSTLocation BOSTON, UNITED STATESPosted 10 Mar 1997Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY2025AR geneAccelerationAcetatesAddressAndrogen ReceptorAndrogenic AgentsAndrogenic CompoundsAndrogensAnti-OncogenesAntioncogenesArmeniaAttentionB7-H1Biologic ModelsBiological FunctionBiological ModelsBiological ProcessBiostatistics CoreCCSGCD274CDK4CDK4 geneCancer CenterCancer Center Support GrantCancer PatientCancer Suppressor GenesCancersCastrate sensitive prostate cancerCatchment AreaCell BodyCell Communication and SignalingCell Division Kinase 4Cell SignalingCellsChIP SequencingChIP-seqChIPseqClinicalClinical InvestigatorClinical TrialsCollaborationsCommunity OutreachCyclin-Dependent Kinase 4DNA mutationDataData ScienceDetectionDevelopmentDihydrotestosterone ReceptorDirect CostsEarly treatmentEmerogenesEnhancersEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessFundingGWA studyGWASGene Down-RegulationGenesGenetic ChangeGenetic defectGenetic mutationGenetsInduction TherapyInstitutionInternationalIntracellular Communication and SignalingInvestigatorsLengthLinkMalignant NeoplasmsMalignant TumorMalignant neoplasm of prostateMalignant prostatic tumorMassachusettsMediatingMetastasisMetastasizeMetastatic LesionMetastatic MassMetastatic NeoplasmMetastatic TumorMissionModel SystemMutateMutationNEOADJNR3C4NatureNeoadjuvantNeoadjuvant TherapyNeoadjuvant TreatmentNeoplasm MetastasisNon-metastaticNonmetastaticOnco-Suppressor GenesOncogenes-Tumor SuppressorsPD-1 blockadePD-L1PD1 blockadePDL-1PSK-J3PaperPatientsPeer Review GrantsPhenotypeProgrammed Cell Death 1 Ligand 1Programmed Death Ligand 1ProstateProstate CAProstate CancerProstate GlandProstate malignancyProstatic GlandPublishingRNA SplicingRecessive OncogenesReportingRepressionResearchResearch DesignResearch PersonnelResearch ResourcesResearchersResistanceResource SharingResourcesSMAX1SamplingSecondary NeoplasmSecondary TumorSeriesSignal TransductionSignal Transduction SystemsSignalingSplicingStructureStudy TypeSurrogate End PointsSurrogate EndpointTherapeutic AndrogenTrainingTranscription RepressionTumor Suppressing GenesTumor Suppressor GenesUpstream EnhancerVariantVariationWorkXtandiabirateroneandrogen ablation therapyandrogen blockade therapyandrogen deprivation therapyandrogen deprivation treatmentandrogen independent prostate cancerandrogen indifferent prostate cancerandrogen insensitive prostate cancerandrogen receptor geneandrogen resistance in prostate cancerandrogen resistant prostate cancerandrogen sensitive prostate cancerantagonismantagonistanti-PD-1 blockadeanti-PD1 blockadebiological signal transductionbiomarker drivencancer biomarkerscancer epidemiologycancer geneticscancer markerscancer metastasiscancer progressioncastration resistant CaPcastration resistant PCacastration resistant prostate cancerchromatin immunoprecipitation coupled with sequencingchromatin immunoprecipitation followed by sequencingchromatin immunoprecipitation with sequencingchromatin immunoprecipitation-seqchromatin immunoprecipitation-sequencingclinical practiceclinical translationclinically translatablecollaboration with communitiescollaborative trialcommunity collaborationcommunity engagementcommunity-based collaborationconstitutive expressionconstitutive gene expressiondetermine efficacydevelopmentalearly therapyefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationengagement with communitiesentire genomeenzalutamideepigeneticallyevaluate efficacyexamine efficacyexome sequencingexome-seqfull genomegene repressiongenome mutationgenome scalegenome sequencinggenome wide associationgenome wide association scangenome wide association studygenome-widegenomewidegenomewide association scangenomewide association studygenomic biomarkergenomic markerglobal gene expressionglobal transcription profilehormone refractory prostate cancerhormone sensitive prostate cancerimprovedimproved outcomein vivoinduction therapiesinhibitorinter-institutionalmalignancymembermenmultidisciplinaryneoplasm progressionneoplasm/cancerneoplastic progressionnext generationnoveloncosuppressor genepatient populationphase 2 trialphase 3 trialphase II trialphase III trialprogrammed cell death ligand 1programmed cell death protein ligand 1programsprostate cancer resistant to androgenprostate cancer riskprotein death-ligand 1resistance mechanismresistantresistant mechanismrisk stratificationstratify riskstudy designtranscriptometumortumor cell metastasistumor progressionwhole genomewhole genome association analysiswhole genome association study
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Full Description

Prostate Cancer Program
Project Summary / Abstract

The Prostate Cancer Program seeks to improve outcomes for all prostate cancer patients by bringing together a multidisciplinary team of investigators across the DF/HCC consortium to catalyze and accelerate research leading to clinical benefit. A founding premise of the Program is that genuine progress in the management of prostate cancer requires iterative fundamental discovery through research in model systems and in patient- derived samples, clinical translation, and subsequent analysis of patient-derived clinical samples to assess mechanisms of action and sensitivity or resistance in vivo. The Program harnesses CCSG structures and resources to achieve this iterative cycle. Additionally, the Program addresses the burden of prostate cancer in our catchment area (Massachusetts) and pays particular attention to training the next generation of basic and clinical investigators across the consortium. The Program’s 66 members (42 primary and 24 secondary) represent seven DF/HCC institutions and 11 academic departments. In 2019, peer-reviewed grant funding attributed to the Program was $2.6 million in direct costs from the NCI and $3.4 million from other sponsors. During the current funding period, primary Program members published 840 cancer-relevant papers. Of these, 27% were inter-institutional, 30% were intra-programmatic, and 31% were inter-programmatic collaborations between two or more DF/HCC members. To achieve the Program mission, our Specific Aims for the next CCSG funding period are to 1) Improve detection and early treatment of aggressive prostate cancer; 2) Identify mechanisms of resistance to current therapies and identify further targetable vulnerabilities; and 3) Exploit tumor specific vulnerabilities through biomarker driven clinical trials. Our work is done in collaboration with the Community Outreach and Engagement (COE) functions of the Cancer Center. In addition, Program members rely heavily on Center collaborative and clinical trials structures and shared resources.

Grant Number: 5P30CA006516-60
NIH Institute/Center: NIH

Principal Investigator: Steven Balk

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