grant

Program 34: Lung Cancer

Organization DANA-FARBER CANCER INSTLocation BOSTON, UNITED STATESPosted 10 Mar 1997Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY2026AccelerationAddressAuthorshipB-raf-1B7-H1BRAFBRAF geneC-K-RASCCSGCD274CT screeningCancer CauseCancer CenterCancer Center Support GrantCancer EtiologyCancer GenesCancer-Promoting GeneCancersCellular biologyClinicClinicalClinical ResearchClinical StudyClinical TrialsCollaborationsCombination immunotherapyDF/HCCDNA mutationDNA seqDNA sequencingDNAseqDana-Farber Cancer InstituteDevelopmentDiagnosisDirect CostsDisciplineDrug resistanceDrugsEGF ReceptorEGFRERBB ProteinEarly DiagnosisElementsEpidermal Growth Factor ReceptorEpidermal Growth Factor Receptor KinaseEpidermal Growth Factor Receptor Protein-Tyrosine KinaseEpidermal Growth Factor-Urogastrone ReceptorsEvolutionFacultyFundingGenetic ChangeGenetic PredispositionGenetic Predisposition to DiseaseGenetic SusceptibilityGenetic defectGenetic mutationGenetic propensityGenomicsGoalsHER1Immune mediated therapyImmunologically Directed TherapyImmunotherapeutic agentImmunotherapyInfrastructureInherited PredispositionInherited SusceptibilityInstitutionInvestigationInvestigatorsK-RAS2AK-RAS2BK-RasK-Ras 2AK-Ras-2 OncogeneKRASKRAS2KRAS2 geneKi-RASLaboratoriesLinkMCF3Malignant CellMalignant NeoplasmsMalignant Thoracic NeoplasmMalignant Thoracic TumorMalignant TumorMalignant Tumor of the LungMalignant Tumor of the ThoraxMalignant neoplasm of lungMalignant neoplasm of thoraxMedicationMentorsMethodsMissionMolecular AnalysisMutationOncogene K-RasOncogenesPD-L1PDL-1PaperPathogenesisPathogenicityPathway interactionsPatientsPeer Review GrantsPharmaceutical PreparationsPlayPopulationPostdocPostdoctoral FellowPredispositionPreventionPreventivePrognosisProgrammed Cell Death 1 Ligand 1Programmed Death Ligand 1PublishingPulmonary CancerPulmonary malignant NeoplasmRAFB1RASK2ROS1ROS1 geneResearchResearch AssociateResearch PersonnelResearch ResourcesResearchersResistanceResource SharingResourcesRoleScreening for cancerSeminalSignal PathwaySignaling MoleculeStaining methodStainsStrategic PlanningStrategic visionStructureSusceptibilityTGF-alpha ReceptorTestingTherapeutic AgentsTherapeutic Clinical TrialTrainingTransforming GenesTransforming Growth Factor alpha ReceptorUnderserved PopulationUrogastrone ReceptorVaccinesc-erbB-1c-erbB-1 Proteincancer carecancer cellcancer geneticscancer immunologycancer microenvironmentcancer riskcancer sub-typescancer subtypescareercease smokingcell biologycheck point blockadecheckpoint blockadechemotherapyclinical developmentcombinatorial immunotherapycommunity engagementcommunity engagement processcomputed tomography screeningdevelopmentaldrug resistantdrug/agentdual immunotherapyearly cancer detectionearly detectionengagement with communitieserbB-1erbB-1 Proto-Oncogene ProteinerbBlfrontiergenetic vulnerabilitygenetically predisposedgenome mutationimmune check point blockadeimmune checkpoint blockadeimmune drugsimmune therapeutic approachimmune therapeutic interventionsimmune therapeutic regimensimmune therapeutic strategyimmune therapyimmune-based therapeuticsimmune-based therapiesimmune-based treatmentsimmuno therapyimmunologic therapeuticsimmunotherapeuticsimmunotherapy agentimprovedinnovateinnovationinnovativeinsightinter-institutionalliquid biopsylung cancerlung cancer early detectionlung cancer screeningmalignancymemberneoplasm immunologyneoplasm/cancernew drug treatmentsnew drugsnew pharmacological therapeuticnew technologynew therapeutic approachnew therapeutic interventionnew therapeutic strategiesnew therapeuticsnew therapynew therapy approachesnew treatment approachnew treatment strategynext generationnext generation therapeuticsnovel drug treatmentsnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel technologiesnovel therapeutic approachnovel therapeutic interventionnovel therapeutic strategiesnovel therapeuticsnovel therapynovel therapy approachpathwaypost-docpost-doctoralpost-doctoral traineepre-clinical studypreclinical studyprogrammed cell death ligand 1programmed cell death protein ligand 1programsprotein death-ligand 1proto-oncogene protein c-erbB-1quit smokingresearch associatesresistance mechanismresistance to Drugresistantresistant mechanismresistant to Drugresponsescreening cancer patientssingle cell analysissmoking cessationsocialsocial rolestop smokingtargeted agenttargeted drug therapytargeted drug treatmentstargeted therapeutictargeted therapeutic agentstargeted therapytargeted treatmentthoracic cancerthoracic malignanciestumortumor DNAtumor cell DNAtumor immunologytumor microenvironmenttumor-specific DNAunder served groupunder served individualunder served peopleunder served populationunderserved groupunderserved individualunderserved peoplev-Ki-RAS2 Kirsten Rat Sarcoma 2 Viral Oncogene Homologv-ROS Avian UR2 Sarcoma Virus Oncogene Homolog 1v-raf Murine Sarcoma Viral Oncogene Homolog B1
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Full Description

Lung Cancer Program Project Summary / Abstract
The Lung Cancer Program conducts innovative research on lung cancer causes and pathogenesis, focusing on discoveries that improve prevention, diagnosis, and therapy. The Program leverages expertise across all DF/HCC institutions in smoking cessation, lung cancer screening, genetic susceptibility, genomic changes in lung cancer, preclinical and clinical studies of novel therapies, and molecular analysis of tumors before and after targeted and immunotherapeutic agents. A core strength of the Program is an integral bidirectional link between the laboratory and clinic, which has enabled insights into drug resistance and accelerated clinical development of agents to overcome newly identified vulnerabilities. Community engagement is embedded in the Program’s laboratory, preventive, cancer screening, and clinical efforts. The Program’s 69 members (51 primary and 18 secondary) represent six DF/HCC institutions and 11 academic departments. In 2019, peer-reviewed grant funding attributed to the Program was $6.5 million in direct costs from the NCI and $2.6 million from other sponsors. During the current funding period, primary Program members published 1,004 cancer-relevant papers. Of these, 27% were inter-institutional, 27% were intra-programmatic, and 42% were inter-programmatic collaborations between two or more DF/HCC members. To achieve the Program mission, we propose the following Specific Aims during the next CCSG funding period: 1) Identify environmental, social, and genomic determinants of lung cancer risk and their role in susceptibility, pathogenesis, and prognosis of lung cancer; 2) Define pathogenic mechanisms that underlie the development and evolution of lung cancer; 3) Exploit the discoveries in cell biology to characterize signaling pathway activated by driver oncogenes to develop novel therapeutic approaches to thoracic malignancies; 4) Characterize the mechanisms of primary and acquired resistance to targeted therapy and develop new methods to overcome resistance; and 5) Identify critical tumor-intrinsic, tumor microenvironment, and host determinants of response to immunotherapy across lung cancer subtypes. Each of these Aims is intimately related to the DF/HCC strategic plan. To achieve them, Program members will depend heavily on CCSG support in the form of shared resources, a clinical trials infrastructure, exceptional collaborative opportunities, processes for community engagement, and established structures to train junior investigators.

Grant Number: 5P30CA006516-61
NIH Institute/Center: NIH

Principal Investigator: David Barbie

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