grant

Tumor Biology Program

Organization UNIVERSITY OF PENNSYLVANIALocation PHILADELPHIA, UNITED STATESPosted 15 Jan 1997Deadline 30 Nov 2027
NIHUS FederalResearch GrantFY2026ATACAbbreviationsAcademyAlpha-Beta-Omega Interferon Receptor-1AmericanAmerican Cancer SocietyAndrogen ReceptorAnti-Cancer AgentsAntineoplastic AgentsAntineoplastic DrugsAntineoplasticsAntiviral Protein Alpha TypeApplied ResearchApplied ScienceAreaArtsAssayAwardBasic Cancer ResearchBasic ResearchBasic ScienceBioassayBiologicalBiological AssayCCSGCancer BiologyCancer CenterCancer Center Support GrantCancer DrugCancer ModelCancerModelCancersCatchment AreaCell BodyCell Communication and SignalingCell SignalingCellsCellular biologyChemoresistanceChromatinClear cell carcinoma of kidneyClear cell renal carcinomaClear cell renal cell carcinomaClinicCollaborationsCommunity OutreachConventional (Clear Cell) Renal Cell CarcinomaConventional Renal Cell CarcinomaDNA MethylationDNA Molecular BiologyDNA SequenceDNA mutationDental SchoolsDetectionDiagnosticDirect CostsDoctor of PhilosophyDrosophilaDrosophila genusEGF ReceptorEGFRERBB ProteinEarly DiagnosisEarly treatmentEducationEducational aspectsEndothelial CellsEngineeringEnvironmentEpidermal Growth Factor ReceptorEpidermal Growth Factor Receptor KinaseEpidermal Growth Factor Receptor Protein-Tyrosine KinaseEpidermal Growth Factor-Urogastrone ReceptorsEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessEpitheliumEyeEyeballFacultyFosteringFundingGene ExpressionGenetic ChangeGenetic defectGenetic mutationGlioblastomaGoalsGrade IV Astrocytic NeoplasmGrade IV Astrocytic TumorGrade IV AstrocytomaGrantHER1HMG DomainHMG ProteinsHMG-1/-2HMG-BHMG-Box ProteinsHMGBHMGB Family GeneHMGB Family ProteinHMGB ProteinsHeritabilityHigh Mobility Group Box ProteinsHigh Mobility Group DomainHigh Mobility Group ProteinsHigh School StudentHuIFN-Alpha-RecIFNARIFNAR1IFNAR1 geneIFNBRIFRCImageImmuneImmune EvasionImmunesIn VitroInflammationInstitutionInterferon Alpha-Beta Receptor Alpha ChainIntermediary MetabolismIntracellular Communication and SignalingKidney Clear Cell AdenocarcinomaKidney Clear Cell CarcinomaLPTNLeadershipMalignant CellMalignant NeoplasmsMalignant TumorMass Photometry/Spectrum AnalysisMass SpectrometryMass SpectroscopyMass SpectrumMass Spectrum AnalysesMass Spectrum AnalysisMedalMedicineMentorsMentorshipMesenchymalMetabolic ProcessesMetabolismMethodsMolecularMolecular BiologyMutationNational Academy of SciencesNational Institutes of HealthNeoplastic Disease Chemotherapeutic AgentsOncogenesisPancreas Ductal AdenocarcinomaPancreatic Ductal AdenocarcinomaPaperPathway interactionsPeer ReviewPennsylvaniaPh D studentPh D. studentPh. D. studentPh.D studentPh.D.Ph.D. studentPhDPhD studentPhD. studentPhiladelphiaPhysiciansPlayPostdocPostdoctoral FellowPreventative strategyPrevention strategyPreventivePreventive strategyProcessPublicationsPublishingRadiation BiologyRadiobiologyRenal Clear Cell AdenocarcinomaRenal Clear Cell CarcinomaResearchResearch AssociateRetinal NeuroblastomaRetinoblastomaRoleSCM-1SCM-1aSCM1SCYC1Scholars ProgramSchoolsScienceScientific PublicationScientistSecondary School StudentSecondary StudentSignal PathwaySignal TransductionSignal Transduction SystemsSignalingSocietiesStromal CellsTGF-alpha ReceptorTechnologyTherapeuticTrainingTranscriptional ControlTranscriptional RegulationTransforming Growth Factor alpha ReceptorTranslatingTransposaseTumor BiologyTumor EscapeTumor Immune EscapeTumor-Specific Treatment AgentsUnited States National Academy of SciencesUnited States National Institutes of HealthUniversitiesUrogastrone ReceptorVeterinary MedicineVeterinary SchoolsViralXCL1XCL1 geneacronymsandrogen independent prostate cancerandrogen indifferent prostate cancerandrogen insensitive prostate cancerandrogen resistance in prostate cancerandrogen resistant prostate canceranti-cancer druganti-cancer researchbiologicbiological signal transductionc-erbB-1c-erbB-1 Proteincancer cellcancer evasioncancer immune escapecancer immune evasioncancer initiationcancer microenvironmentcancer progressioncancer researchcastration resistant CaPcastration resistant PCacastration resistant prostate cancerccRCCcell biologychemoresistantchemotherapy resistancechemotherapy resistantchimeric antigen receptorclinical investigationcommunity engagementconferenceconventiondoctoral studentdrug sensitivityearly detectionearly therapyengagement with communitiesenvironmental carcinogenesisepigenetic regulationepigeneticallyepithelial to mesenchymal transitionerbB-1erbB-1 Proto-Oncogene ProteinerbBlfruit flygenome integritygenome mutationgenomic integrityglioblastoma multiformehigh schoolershistone modificationhormone refractory prostate cancerifnar1 gene productimagingimaging programimmune evasivein vivo Modelinnovateinnovationinnovativeinsightinterestmalignancymedical collegemedical schoolsmeetingmeetingsmembermimicryneoplasm progressionneoplasm/cancerneoplastic progressionnoveloptogeneticspathwaypost-docpost-doctoralpost-doctoral traineeprognosticprogramsprostate cancer resistant to androgenprotein Bproto-oncogene protein c-erbB-1recruitresearch associatesretina neuroblastomaschool districtschool of medicinesocial rolespongioblastoma multiformesuccesssummitsymposiasymposiumtobacco carcinogenesistumortumor evasiontumor growthtumor immune evasiontumor initiationtumor microenvironmenttumor progressiontumorigenesistype I IFN receptortype I interferon receptorundergradundergraduateundergraduate student
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Full Description

The Tumor Biology Program is one of two basic science Research Programs of the Abramson Cancer Center (ACC). This Program aims to catalyze research within the ACC to advance an understanding of mechanisms underlying tumorigenesis and to identify pathways that will enable novel preventive, diagnostic, prognostic and therapeutic approaches to cancer. Since its inception in the early 1970s, the Tumor Biology Program has continued to respond to emerging areas and advances in cancer research. The Program is currently organized around three central Aims: 1) Elucidate the molecular and cellular basis underlying cancer; 2) Understand the epigenetics of cancer; and 3) Investigate the tumor microenvironment and metastatic progression.

Members of Tumor Biology are highly interactive, collaborating intra-Programmatically across scientific topics relevant to each Aim including genome integrity, cell signaling, metabolism, and viral pathways, with an eye on cancers of highest relevance to our catchment area. Ground-breaking discoveries in Tumor Biology uncovered novel mechanisms of epithelial-mesenchymal transition, transcriptional control of cancer drug sensitivity, epigenetic regulation of inflammation, novel mechanisms of androgen-resistance in prostate cancer, and immune evasion by viral mimicry. New targets were translated to the clinic in collaboration with other Programs for early detection and treatment. The Tumor Biology Program is led by new and energetic Program co-Leaders (PLs) Shelley Berger, PhD and Sandra Ryeom, PhD, who together catalyze impactful intra- and inter-Programmatic collaborations by a variety of innovative methods.

The PLs are instrumental in recruiting new members, mentoring junior faculty, stimulating interactions and meetings among faculty members, and organizing conferences and symposia. Tumor Biology Program members play key roles in the training and mentorship of high school students, PhD students, MD/PhD students, and MD or PhD postdoctoral fellows in cancer-related research through their leadership roles in the University of Pennsylvania Biomedical Graduate Studies (BGS), MD/PhD program (MSTP) and NIH T32 training grants. The continued success of the Tumor Biology Program is evidenced by the exceptional scientific progress of its members, demonstrated through high-impact publications with multi-institutional, inter- and intra-Programmatic collaborations, offering key insights into the biology of cancer. Currently, the Program has 53 members from 20 departments and five different schools with total funding of $25.7M (annual direct costs) of which 20.0M is peer-reviewed and $6.4M is NCI-funded.

The Program has 67 R01-equivalents. Since 2015, Tumor Biology Program members published 617 cancer-related papers, of which 15% were intra-Programmatic, 29% were inter-Programmatic, and 62% were multi-institutional.

Grant Number: 4P30CA016520-50
NIH Institute/Center: NIH

Principal Investigator: SHELLEY BERGER

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