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Epstein-Barr Virus LMP-1 Mediated Oncogenicity

Epstein-Barr Virus LMP-1 Mediated Oncogenicity
Epstein-Barr 病毒 LMP-1 介导的致癌性
批准号:
7460802
负责人:
ELLIOTT D KIEFF
金额:
$72.69万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-09-20 至 2011-06-30
关键词:
Acquired Immunodeficiency SyndromeAffectAffinityAmino AcidsApoptosisB-LymphocytesBiochemicalBiochemical GeneticsBiologicalBiological AssayC-terminalCell NucleusCell membraneCellsCessation of lifeChemicalsClassificationComplexCytoplasmic TailDeubiquitinating EnzymeDifferentiation and GrowthEBV-associated diseaseElementsEpithelial CellsEpstein-Barr Virus InfectionsEpstein-Barr virus LMP-1 proteinFibroblastsFluorescence Resonance Energy TransferGeneticGenetic ScreeningHIV InfectionsHeat-Shock Proteins 90Hematologic NeoplasmsHerpesviridaeHodgkin DiseaseHuman Herpesvirus 4HypersensitivityImmuneImmune System DiseasesIn VitroIndividualInterruptionKnock-outKnowledgeLigandsLymphocyteLymphocyte ActivationLymphoproliferative DisordersMAP Kinase Signaling PathwaysMAP3K7 geneMAPK14 geneMAPK8 geneMalignant NeoplasmsMediatingMembraneMembrane ProteinsMethodologyMolecular TargetMutationNF-kappa BNasopharynx CarcinomaNumbersOncogenicPathway interactionsPatientsPharyngeal CarcinomaPhosphoric Monoester HydrolasesPhosphotransferasesPlasmaPreventionProliferatingProteinsProteomicsRNA InterferenceRegulatory ElementRelative (related person)ResearchResearch PersonnelRoleScaffolding ProteinSignal PathwaySignal TransductionSignaling MoleculeSiteSmall Interfering RNATBK1 geneTESTNF Receptor-Associated Death Domain ProteinTNF receptor-associated factor 2TNF receptor-associated factor 3TNF receptor-associated factor 6TNFRSF1A geneTNFRSF1B geneTRADD geneTRAF2 geneTRAF6 geneTechnologyTranscriptional ActivationTransmembrane DomainTransplant RecipientsTransplantationTumor Necrosis Factor ReceptorValidationbasecell growthchemical geneticsdrug discoveryhuman diseaseinhibitor/antagonistinsightlymphoblastlymphoblastoid cell linemonomerneurotensin mimic 1novelnovel therapeuticspositional cloningprogramspromoterresearch studytherapeutic targettooltumorubiquitin ligase

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中文摘要
翻译
描述(由申请人提供):本研究项目专注于爱泼斯坦-巴尔病毒潜伏膜蛋白1 (LMP1)信号传导,特别是通过遗传和化学方法鉴定LMP1介导的NF-kB激活和靶标验证的关键分子靶标。具体目标1是利用反向遗传、生化和荧光共振能量转移方法表征LMP1跨膜相互作用,这些相互作用对LMP1介导的NF-kB激活至关重要。在这些研究中获得的知识可能使跨膜聚集和信号传导中断。具体目标2侧重于通过串联亲和下拉实验表征TRAF2、TRAF3、NIK、TRADD、TRAF6和IRAKI相关蛋白,鉴定LMP1 TES1和TES2 NF-kB激活缺失成分。通过使用siRNA技术在B淋巴细胞和上皮细胞中进行定向敲除,评估可能的信号成分在NF-kB激活中的作用。基于siRNA的遗传筛选也将用于鉴定NF-kB通路的基本成分。特异性目标3是基于细胞筛选LMP1诱导的NF-KB的新型化学抑制剂,这些抑制剂可以作为新疗法的化学核心。这些工具化合物的目标也将被确定。NF- kB活性是EBV转化b淋巴细胞存活所必需的。因此,LMP1 NF- kB激活抑制剂将有助于治疗LMP1表达的EBV相关疾病,包括艾滋病患者和移植受者的淋巴增生性疾病、霍奇金病和鼻咽癌。鉴于NF-kB活性在淋巴细胞活化、生长、分化和存活中的重要性,一种工具化合物也可能为适用于过敏、移植或自身免疫性疾病的药物发现提供方向。
英文摘要
DESCRIPTION (provided by applicant): This research program focuses on Epstein-Barr virus Latent membrane protein 1 (LMP1) signaling, particularly the identification of molecular targets critical for LMP1-mediated NF-kB activation and target validation through genetic and chemical approaches. Specific objective 1 is to characterize LMP1 transmembrane interactions that are critical for LMP1 mediated NF-kB activation using reverse genetic, biochemical and fluorescence resonance energy transfer methodologies. Knowledge gained in these studies may enable interruption of transmembrane aggregation and signaling. Specific objective 2 focuses on identifying missing components of LMP1 TES1 and TES2 NF-kB activation by characterizing TRAF2, TRAF3, NIK, TRADD, TRAF6 and IRAKI associated proteins by tandem affinity pull-down experiments. Putative signaling components will be evaluated for their role in NF-kB activation by directed knock out using siRNA technology in B lymphocytes and epithelial cells. An siRNA based genetic screen will also be used to identify essential components of the NF-kB pathway. Specific objective 3 is a cell based screen for novel chemical inhibitors of LMP1 induced NF-KB that can serve as a chemical nucleus for novel therapeutics. The targets of such tool compounds will also be determined. NF- kB activity is required for EBV transformed B-lymphocyte survival. Thus inhibitors of LMP1 NF- kB activation will be useful for treating EBV associated diseases where LMP1 is expressed including lymphoproliferative disease in AIDS patients and transplant recipients, Hodgkin's disease, and Nasopharyngeal carcinoma. Given the importance of NF-kB activity in lymphocyte activation, growth, differentiation and survival, a tool compound might also provide direction for drug discovery applicable for allergy, transplantation, or auto immune disease.
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