grant

Comparative Oncology Program

Organization UNIVERSITY OF CALIFORNIA AT DAVISLocation DAVIS, UNITED STATESPosted 1 Jul 2002Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY2025AccelerationAddressAnimal ModelAnimal Models and Related StudiesAnimalsAnti-OncogenesAntioncogenesAreaBasic ResearchBasic ScienceBiologic ModelsBiological ModelsBiologyCCSGCancer BurdenCancer Center Support GrantCancer DiagnosticsCancer PatientCancer Suppressor GenesCancer TreatmentCancersCanine SpeciesCanis familiarisCatchment AreaCell Communication and SignalingCell SignalingCellular OncogeneCenter Core GrantsClinicalClinical InvestigatorCollaborationsComprehensive Cancer CenterDevelopmentDirect CostsDogsDogs MammalsEarly InterventionEmerogenesFosteringFundingGeneticGenetic EngineeringGenetic Engineering BiotechnologyGenetic Engineering Molecular BiologyGenetic InductionGoalsHumanImmune mediated therapyImmunochemical ImmunologicImmunologicImmunologicalImmunologicallyImmunologically Directed TherapyImmunologicsImmunologyImmunotherapyIn VitroIndividualInstitutionIntracellular Communication and SignalingIntratumoral heterogeneityInvestigationInvestigatorsJournalsKnowledgeLeadershipMagazineMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant NeoplasmsMalignant TumorMetabolicMetastasisMetastasizeMetastatic LesionMetastatic MassMetastatic NeoplasmMetastatic TumorMiceMice MammalsMissionModel SystemModern ManMolecularMurineMusNational Cancer BurdenNeoplasm MetastasisNeoplastic ProcessesOnco-Suppressor GenesOncogenes-Tumor SuppressorsOncogenic VirusesOncologyOncology CancerP30 AwardP30 GrantP30 MechanismP30 ProgramPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPeer ReviewPilot ProjectsPre-Clinical ModelPreclinical ModelsProductivityProto-OncogenesPublicationsPublishingRecessive OncogenesRecombinant DNA TechnologyReportingResearchResearch PersonnelResearch ResourcesResearchersResource SharingResourcesRiskSchoolsScienceScientific PublicationScientistSecondary NeoplasmSecondary TumorSignal PathwaySignal TransductionSignal Transduction SystemsSignalingTherapeuticTrainingTraining ProgramsTranslatingTranslational ResearchTranslational ScienceTranslationsTumor BiologyTumor Suppressing GenesTumor Suppressor GenesTumor VirusesVeterinariansViral Oncogeneanti-cancer researchanti-cancer therapybiological signal transductionc-ONCcancer metastasiscancer microenvironmentcancer researchcancer therapycancer-directed therapycaninecollegecollegiatecompanion animalcompanion petcomparativedevelopmentaldomestic dogfirst in manfirst-in-humangenetically engineeredheterogeneity in tumorsimmune therapeutic approachimmune therapeutic interventionsimmune therapeutic regimensimmune therapeutic strategyimmune therapyimmune-based therapiesimmune-based treatmentsimmuno therapyinnovateinnovationinnovativeinsightintra-tumoral heterogeneityintratumor heterogeneitymalignancymembermodel of animalneoplasm/cancernew technologynext generationnovelnovel technologiesoncogenic tumor virusoncology programoncosuppressor genepatient oriented outcomespilot studypre-clinicalpre-clinical trialpreclinicalpreclinical trialpreventpreventingprogramsprotooncogenetranslationtranslation researchtranslational investigationtranslational pipelinetranslational spectrumtumor cell metastasistumor heterogeneitytumor initiationtumor microenvironment
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Full Description

COMPARATIVE ONCOLOGY PROGRAM (COP)
PROJECT SUMMARY/ABSTRACT

The central theme of the Comparative Oncology Program (COP) is to conduct impactful basic and translational

research, including preclinical trials in companion animals, that generates knowledge to prevent and/or reduce

the cancer burden in the UC Davis Comprehensive Cancer Center (UCDCCC) catchment area and beyond.

The Program brings together basic comparative researchers, veterinary scientists, veterinarians, and clinicians

with expertise in trans-species biology and innovative animal models with the goal of generating discoveries

that inform, de-risk and cross-validate early interventional investigations in a preclinical setting before and

during first-in-human trials. COP has three Specific Aims that encompass the full spectrum of research

performed by Program members. Aim 1 is to elucidate the molecular and cellular mechanisms by which

cellular and viral oncogenes and tumor suppressor genes are involved in tumor initiation, progression, and

metastasis. Aim 2 is to characterize metabolic and immunologic tumor heterogeneity to inform cancer

diagnostics and treatment. Aim 3 is to conduct preclinical trials using companion animal cancer patients in

order to inform human cancer research and promote translation, especially in the area of innovative

immunotherapy. Dr. Xinbin Chen, DVM, PhD (basic comparative scientist), Dr. Michael Kent DVM, MAS

(canine clinical trialist), and Dr. Robert Canter, MD (cross-species immunology and immunotherapy) are co-

leaders for COP. The Program’s research portfolio spans the comparative cancer research continuum, from

studies investigating cell signaling pathways in vitro to preclinical trials in companion animals. COP has 20 full

members from three schools/colleges and 12 departments at UC Davis. COP’s total cancer relevant funding is

$5M annual direct cost, including $4.8M in peer-reviewed and $2.8M in NCI funding. The total number of

publications is 365 of which 23% are intra-programmatic, 39% inter-programmatic, 47% multi-institutional, and

24% are published in high impact journals. As a strong Program that is expected to become even more

important to the UCDCCC translational pipeline in the next reporting period, the UCDCCC has established

more robust and frequent transdisciplinary fora and discretionary funding support to the COP, providing its

leadership the ability to support pilot projects that will result in team science comparative cancer research.

Grant Number: 5P30CA093373-23
NIH Institute/Center: NIH

Principal Investigator: Xinbin Chen

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