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DNA Damage and Cellular Defense

DNA Damage and Cellular Defense
DNA 损伤和细胞防御
批准号:
7529422
负责人:
ALAN J TOWNSEND
金额:
$1.14万
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:
AccountingAcridinesAlkylating AgentsAlkylationAlternative MedicineAnimal Cancer ModelAnimalsAntioxidantsApoptosisApoptoticApplications GrantsAreaAwardBasic ScienceBiochemistryBiological AssayBiologyBypassCancer CenterCancer EtiologyCarcinogensCarrier ProteinsCategoriesCell CycleCell DeathCellsCervical Intraepithelial NeoplasiaChemical AgentsChemicalsChemistryChemopreventionChemopreventive AgentClassClinical ResearchClinical TrialsCollaborationsComprehensive Cancer Center of Wake Forest UniversityCultured CellsCurcuminCytotoxic ChemotherapyCytotoxic agentDNADNA AdductsDNA DamageDNA RepairDNA Repair PathwayDNA SequenceDNA biosynthesisDNA lesionDNA-Directed DNA PolymeraseDefectDefense MechanismsDevelopmentDiagnosisDithiolthioneDrug Metabolic DetoxicationDrug resistanceEarly DiagnosisEnzyme InductionEnzymesEvolutionExperimental GeneticsExposure toFacultyFailureFerritinFoundationsFundingFutureGenesGeneticGenetic CounselingGenomicsGerm-Line MutationGlutathioneGlutathione S-TransferaseGoalsGrantGrowthHumanHydroxyl RadicalIndividualInvestigationIonizing radiationIronIron ChelationKnowledgeLearningLesionLife StyleLinkMaintenanceMalignant NeoplasmsMalignant neoplasm of lungMammalian CellMediatingMembraneMetabolic ActivationMismatch RepairModificationMolecular StructureMutagenesisMutagensMutationNADPH OxidaseNatureNumbersOncogenicOxidantsOxidation-ReductionOxidative StressPathologic MutagenesisPathway interactionsPeer ReviewPharmaceutical PreparationsPhasePhenotypePilot ProjectsPlatinum CompoundsPlayPopulationPredispositionPreventionProcessProductionProductivityPrognostic MarkerProteinsPublicationsRadiationRadiation therapyRadiation-Sensitizing AgentsRadioRangeRapid Access to Intervention DevelopmentReactive Oxygen SpeciesRecruitment ActivityRecurrenceRegulationRegulator GenesReplication ErrorResearchResearch PersonnelResistanceResolvaseRoleScientistServicesSignal TransductionSingle-Stranded DNASolutionsSourceSpecificitySubgroupSulfurSulindacTestingTherapeuticTopical applicationToxic effectTranslatingTranslational ResearchTranslationsWaterWorkXenobioticsaging populationanaloganticancer researchbasebrain irradiation injurycaffeic acid phenethyl estercancer cellcancer diagnosiscancer preventioncancer riskcancer therapycarcinogenesiscell growthcell injurychemical carcinogenchemotherapeutic agentchemotherapycysteinesulfenic acidcytotoxiccytotoxicitydemographicsdrug developmentdrug efficacyenvironmental carcinogenesisexpression cloninghuman studyimprovedinnovationinterestkillingsmacromoleculememberneoplastic cellnovelnovel therapeuticsoltiprazprenatalpreventprogramsrepairedresponsesensorspleen exonucleasethree dimensional structuretrendtumor

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中文摘要
翻译
DNA损伤和细胞防御(DDCD)计划是一个由23名成员组成的高度互动的小组, 维克森林大学综合癌症中心,代表7个部门和部门。的 DDCD计划的总体科学目标是了解机制和过程, 细胞维持-或替代地,通过预防或修复来减轻-对DNA或其他关键细胞的损伤。 大分子结构该计划鼓励翻译策略,采用或小说 化学治疗剂或化学预防剂。DDCD计划中的研究重点可以代表 在两个主题目标:1)确定DNA和其他大分子的损伤机制, 化学试剂或辐射,以及这种损害如何导致有害的致癌作用或有益的 抗癌作用(在化学和放射治疗);和2)确定细胞防御机制, 在预防癌发生和调节肿瘤对细胞毒性化疗的敏感性方面的作用, 放射治疗DDCD计划拥有强大的资金和生产力记录。NCI和其他共计 自上次审查以来,同行审查的资金从181万美元增加到628万美元,增加了两倍多。成员 互动性强,203份计划内出版物中有54份(26.6%)和18份计划间出版物 出版物(8.9%)。此外,一些赠款共同赞助机构已成立, 新的合作(66.7%的赠款与另一个CCCWFU成员有正式合作)。成员 依靠CCCWFU核心实验室服务来支持他们的研究,并有效地利用CCCWFU 试点供资:许多试点项目已发展到赠款申请阶段,有些项目已成为有资金支持的赠款。的 该计划以双周研讨会的形式举行,并举行年度务虚会。三个新的月息 小组已经开始,一个关于抗氧化酶的信号功能,第二个关于DNA损伤, 修复和诱变,以及第三组临床医生和基础科学家开发新的翻译 肺癌的研究合作。
英文摘要
The DNA Damage and Cellular Defense (DDCD) Program is a highly interactive group of 23 members of the Comprehensive Cancer Center of Wake Forest University, representing 7 Departments and Sections. The overall scientific goal within the DDCD Program is to understand the mechanisms and processes whereby cells sustain - or alternatively, mitigate by prevention or repair - damage to DNA or other critical macromolecular structures. The Program encourages translational strategies that employ either novel chemotherapeutics or chemopreventive agents. Research focus in the DDCD program can be represented within two thematic aims: 1) To determine mechanisms of damage to DNA and other macromolecules by chemical agents or radiation, and how this damage results in detrimental carcinogenic effects or beneficial anticancer effects (in chemc¿ and radiation therapy); and 2) To identify cellular defense mechanisms that function in prevention of carcinogenesis and modulation of tumor sensitivity to cytotoxic chemotherapy and radiation therapy. The DDCD Program has a strong funding and productivity record. Total NCI and other peer-reviewed funding has more than tripled from $1.81M to $6.28M since the previous review. Members are highly interactive, with 54 of 203 intra-programmatic publications (26.6%) and 18 inter-programmatic publications (8.9%). Also, a number of grant co-investigatorships have resulted from both established and new collaborations (66.7% of grants have a formal collaboration with another CCCWFU member). Members rely on CCCWFU core lab services in support of their research, and have made efficient use of CCCWFU pilot funding: many pilot projects have matured into grant applications and some into funded grants. The Program meets in a biweekly seminar format, and holds an annual retreat. Three new monthly interest subgroups have begun, one on signaling functions of antioxidant enzymes, a second on DNA damage, repair, and mutagenesis, and a third group of clinicians and basic scientists to develop new translational research collaborations in lung cancer.
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