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Cell Growth and Survival

Cell Growth and Survival
细胞生长和存活
批准号:
7529427
负责人:
DOUGLAS S. LYLES
金额:
$1.58万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-07-11 至 2012-01-31
关键词:
AffectAntiviral AgentsAntiviral ResponseApoptosisApoptoticAppointmentAreaBasic ScienceBiochemistryBioinformaticsBiological MarkersBiologyBiostatistics CoreBrain NeoplasmsBreastBreast Cancer TreatmentCancer BiologyCancer Cell GrowthCancer CenterCancer ControlCell DeathCell ProliferationCell Proliferation RegulationCellsCessation of lifeClinical ResearchClinical TrialsCollaborationsColoradoComplementary and alternative medicineComprehensive Cancer Center of Wake Forest UniversityComputational BiologyCore FacilityCultured CellsDNA SequenceData AnalysesDendritic CellsDevelopmentDietary FactorsDietary FatsDietary InterventionDirect CostsElectron Microscopy FacilityEmployee StrikesEndoplasmic ReticulumEnzymesEpidemiologic StudiesEpithelial CellsFacultyFluorescenceFocus GroupsFundingGene ExpressionGenerationsGenesGeneticGenetic PolymorphismGenomicsGliomaGoalsGrowthHeart DiseasesHumanHypoxiaImmuneImmune responseImmunityImmunologic SurveillanceImmunologistIndiumInduction of ApoptosisInflammationInflammatoryInstitutesInvestigationIrisIsoflavonesLaboratoriesLeadLeadershipLeftLinkLipidsMalignant NeoplasmsMalignant neoplasm of prostateMass Spectrum AnalysisMathematicsMediatingMetabolismMicroscopyModelingModificationMolecular TargetMusMutant Strains MiceNatural ImmunityNeoplasm MetastasisOncolytic virusesOxidation-ReductionOxygenOxygen measurement, partial pressure, arterialPathway interactionsPatientsPeer ReviewPhosphoric Monoester HydrolasesPlatelet Activating FactorPlayPolyunsaturated Fatty AcidsPositioning AttributePost-Translational Protein ProcessingPredispositionPreventionPrimatesProcessProductionProductivityProstateProstaticProtein AnalysisProteinsProteomicsPublishingRadiation therapyRadiosensitizationReactive Oxygen SpeciesRecombinantsRecruitment ActivityRegulationReportingResearchResearch PersonnelResearch Project GrantsResistanceResourcesRiskRodent ModelRoleSamplingSeriesSignal PathwaySignal TransductionSignaling MoleculeSolid NeoplasmSpecimenStandards of Weights and MeasuresStressSystems BiologyT-LymphocyteTechnologyTherapeuticThinkingTimeToll-like receptorsTranscriptional RegulationTranslatingTranslational ResearchTranslationsTumor TissueUniversitiesViral GenomeViral VectorVirginiaVirusVirus AssemblyVirus DiseasesVitamin DVitamin D AnalogWorkZemplaranticancer researchbasebench to bedsidebiological adaptation to stresscancer cellcancer therapycell growthcell growth regulationcell injurychemotherapeutic agentcomputer scienceconceptcysteinesulfenic acidfascinateforestimprovedinterestkillingslycopenemalignant breast neoplasmmedical schoolsmembermultidisciplinarymutantneoplastic cellnovelnovel strategiesoutcome forecastprofessorprogramsprohormonerapid growthsoysoy protein isolatesuccesssynergismtraittranscription factortumortumorigenesisvirus host interaction

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英文摘要
The Cell Growth and Survival (CGS) Program is focused on the signaling pathways that regulate the growth, survival and death of normal and neoplastic cells. The goal of this research is to develop novel strategies that exploit this understanding to improve anti-cancer therapy. The CGS Program currently has 27 scientific members from 10 departments in the Wake Forest University School of Medicine. Changes in membership of the CGS program since the previous review in 2000 reflect specific, targeted recruiting to improve integration of the major themes of the program. These changes are now paying dividends in terms of scientific productivity. This program has undergone substantial growth in its total funding, from $2.44M to S4.38M direct costs in annual peer-reviewed funding. In addition, the extent of scientific collaboration has increased markedly during the present funding period, centered on the major themes of the Program. CGS Program members published 242 peer-reviewed articles in 2001-2005. Of these, 20% had at least two CGS program members as coauthors, compared to 5% in the review in 2000. In 2004, Dr. Douglas Lyles, Professor and Chair of Biochemistry, was appointed as Director of the CGS Program (the previous director, Dr. Thorburn, left to assume a cancer center leadership position at University of Colorado). Dr. Lyles has been a member of the CCCWFU for 26 years. His research on virus assembly and virus-host interactions has led to new ideas for the development of novel oncolytic viruses for the treatment of cancer. He assumed the chairmanship of the Department of Biochemistry in 2004 with a strong commitment to recruit new faculty in cancer research and to continue to strengthen the substantial existing relationship between the Department of Biochemistry and the CCCWFU. Dr. Lyles' appointment has further integrated efforts in faculty development within this program. The following sections highlight selected major themes in the CGS program. Several novel contributions from the CGS Program to the national cancer effort have emerged as themes since the previous review. They are: 1) a fascinating synergy between vitamin D and dietary soy isoflavones in regulation of proliferation in prostate and breast cancer; 2) explorations of the effects of dietary lipids on cancer cell proliferation and metastasis; 3) a novel role of reactive oxygen species as signaling molecules in cell proliferation; 4) translational control and endoplasmic reticulum stress in hypoxia, 5) the genetic control of innate anti-tumor immune mechanisms; and 6) the antagonistic relationship of antiviral and proliferative signaling and the development of novel oncolytic viruses. These themes directly reflect the value-added as a result of the CCCWFU: thematic development and faculty recruiting by the Cancer Center leadership; shepherding the development of these themes by the Program Director; a high degree of collaboration within the CGS and with other Programs, major participation in the Centers of Excellence, and effective use of shared facilities.
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