grant

Cancer Cell Biology Research Program

Organization VANDERBILT UNIVERSITY MEDICAL CENTERLocation NASHVILLE, UNITED STATESPosted 1 Sept 1998Deadline 31 Aug 2027
NIHUS FederalResearch GrantFY2025ABC20ABCB1ABCB1 geneAccelerationAffectAffinityAndrogen ReceptorApoptoticBasic ResearchBasic ScienceBioavailabilityBiological AvailabilityBiologyBiomedical EngineeringCCSGCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCancer CenterCancer Center Support GrantCancer InterventionCancersCapraCas nuclease technologyCatchment AreaCell BodyCell Communication and SignalingCell CycleCell Cycle ControlCell Cycle RegulationCell DifferentiationCell Differentiation processCell Division CycleCell SignalingCellsCellular biologyChemicalsChemoresistanceChimeraChimera organismClinicClinicalClinical InvestigatorClinical TrialsClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyCollaborationsCommunicationComputational toolkitCytometryDNA mutationDependenceDevelopmentDoctor of PhilosophyDrugsEGFEGF ReceptorEGF geneEGFREGFR BlockerEGFR InhibitorEGFR Tyrosine Kinase InhibitorEGFR-TK InhibitorERBB ProteinEducational workshopEffectivenessEnsureEpidermal Growth Factor ReceptorEpidermal Growth Factor Receptor InhibitorEpidermal Growth Factor Receptor KinaseEpidermal Growth Factor Receptor Protein-Tyrosine KinaseEpidermal Growth Factor Receptor Tyrosine Kinase InhibitorEpidermal Growth Factor-Urogastrone ReceptorsErinaceidaeFacultyFosteringFundingFutureGP170Gene ExpressionGenetic ChangeGenetic defectGenetic mutationGenus CapraGerm LinesGoalsHER1HedgehogsHeterogeneityHistoryHumanImage CytometryIntracellular Communication and SignalingInvestigationInvestigatorsKnock-inLeadershipLightMDR-1MDR1MDR1 ProteinMalignant CellMalignant NeoplasmsMalignant TumorMedicationMentorsMentorshipMethodsMiceMice MammalsMicroscopyMissionModern ManModernizationMultidrug Resistance 1Multidrug Resistance Gene-1Multidrug Resistance Gene-1sMultidrug Resistance ProteinsMultidrug Resistant ProteinsMurineMusMutationNCI-Designated Cancer CenterOncogenesisP-GPP-GlycoproteinP-Glycoprotein 1 GeneP01 MechanismP01 ProgramPGY-1 ProteinPGY1Pathway interactionsPatientsPeer ReviewPh.D.PhDPharmaceutical PreparationsPhotoradiationPhysicsPhysiologic AvailabilityPlayPopulation ProgramsProgenitor CellsProgram Project GrantProgram Research Project GrantsProliferatingPublicationsRecording of previous eventsReproducibilityResearchResearch PersonnelResearch Program ProjectsResearchersResource SharingRoleSHHSHH geneSchoolsScienceScientific PublicationScientistSignal PathwaySignal TransductionSignal Transduction SystemsSignalingSonic HedgehogStructural ModelsStudentsTGF-alpha ReceptorTechnologyTestingTherapeuticTherapeutic InterventionTrainingTransforming Growth Factor alpha ReceptorTranslatingTranslationsTumor Cell BiologyUrogastrone ReceptorWorkWorkshopanti-cancer researchbench bed sidebench bedsidebench to bed sidebench to bedsidebench to clinicbench to clinical practicebio-engineeredbio-engineersbioengineeringbiological engineeringbiological signal transductionc-erbB-1c-erbB-1 Proteincancer cellcancer initiationcancer progressioncancer researchcapridcell biologycellular differentiationchemoresistantchemotherapy resistancechemotherapy resistantchimerascomputational toolboxcomputational toolscomputational toolsetcomputerized toolscostdesigndesigningdevelopmentaldrug discoverydrug/agenterbB-1erbB-1 Proto-Oncogene ProteinerbBlgenome editinggenome mutationgenomic editinghistoriesindustrial partnershipindustry partnerindustry partnershipinhibitorinstrumentationintervention therapyknockinmalignancymeetingmeetingsmembermulti drug transportermultidrug transporterneoplasm progressionneoplasm/cancerneoplastic progressionnew drug targetnew drug treatmentsnew druggable targetnew drugsnew pharmacological therapeuticnew pharmacotherapy targetnew technologynew therapeutic targetnew therapeuticsnew therapynew therapy targetnext generation therapeuticsnovelnovel drug targetnovel drug treatmentsnovel druggable targetnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel pharmacotherapy targetnovel technologiesnovel therapeutic targetnovel therapeuticsnovel therapynovel therapy targetpathwaypopulation basedprogenitor cell proliferationprogenitor proliferationprogramsproto-oncogene protein c-erbB-1resistance mechanismresistant mechanismresponsescRNA sequencingscRNA-seqsingle cell RNA-seqsingle cell RNAseqsingle cell expression profilingsingle cell transcriptomic profilingsingle-cell RNA sequencingsmall moleculesocial rolestem and progenitor cell proliferationstem cell proliferationstem cellssuperresolution microscopytherapeutic targettranslationtumortumor progressiontumorigenesis
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Full Description

PROJECT 002– SIGNAL TRANSDUCTION AND CHEMICAL BIOLOGY RESEARCH PROGRAM
PROJECT SUMMARY/ABSTRACT

The Signal Transduction and Chemical Biology Research Program (ST) pursues fundamental cancer research

to understand patient- and cancer-specific rewiring of signaling networks and the cell cycle, and how

stem/progenitor cell plasticity and heterogeneity contribute to tumorigenesis. This information is used to identify

new targets that could be the focus of future drug discovery efforts. Accordingly, an overarching goal of ST is to

develop novel and/or test small molecule leads against important drivers of cancer initiation and progression and

aid the optimization of `leads' to drugs so that ST discoveries can be translated to the clinic as new cancer

interventions. The major role of ST leadership is to ensure communication between clinical investigators,

population-based researchers and basic scientists to ensure that potentially translatable findings are explored.

ST leadership and Vanderbilt-Ingram Cancer Center (VICC) sponsor meetings and retreats to ensure that

communication of the basic science discoveries is robust. Program goals will be accomplished by: 1) performing

cutting-edge research in single cell biology, stem cells and signaling networks, to identify key targets that confer

selective dependencies in human cancers; 2) promoting cutting edge research in chemical biology and

development of new cancer therapeutics; and 3) stimulating interactions among the Program membership to

accelerate discovery, mentor junior faculty, foster collaborations with clinical programs, promote technologies

such as scRNA-seq, super-resolution microscopy, mass cytometry and PROTACS, and work closely with VICC

Shared Resources to develop new instrumentation for cancer discovery. There are 44 program members from

13 departments and four schools with $11M in total peer-reviewed funding and NCI making up 39% ($4.3M).

Out of 372 publications, 15% are intra-programmatic and 34% are inter-programmatic. Members also have 115

collaborative publications with investigators at other NCI-designated cancer centers.

Grant Number: 4P30CA068485-30
NIH Institute/Center: NIH

Principal Investigator: Jin Chen

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