Small Molecule Inhibitors of the Transcriptional Activators ESX and NF-kB
Small Molecule Inhibitors of the Transcriptional Activators ESX and NF-kB
批准号:
8444638
负责人:
ANNA K. MAPP
金额:
$27.64万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-05-20 至 2015-02-28
关键词:
Activator AppliancesAddressAffectApoptosisBindingBiological AssayBiological FactorsBreast Cancer CellCancer cell lineCell Culture TechniquesCell surfaceCellsCharacteristicsComplexDiseaseDoseEffectivenessExhibitsFutureGene ExpressionGenerationsGeneric DrugsGenesGeneticGenetic TranscriptionGrowthGrowth and Development functionHead CancerHeart DiseasesHumanIn VitroIndividualInvestigationLaboratoriesLeadLibrariesMalignant NeoplasmsMalignant neoplasm of pancreasMarinesMediatingMessenger RNAModelingMolecularNF-kappa BNeck CancerNeoplasm MetastasisNormal tissue morphologyPathway interactionsPatternPharmaceutical PreparationsPhenotypeProcessProteinsRegulationRegulatory PathwayReporterReportingResistanceRoche brand of trastuzumabSignal TransductionSourceSpecificityTNFRSF5 geneTestingTherapeuticTherapeutic AgentsTranscription CoactivatorTranscription InitiationTranscriptional ActivationTranscriptional Activation DomainTyrosine Kinase Inhibitorbasecell motilitychemotherapydesigngenome-widehigh throughput screeninghuman diseasehydrastinein vivoin vivo Modelinhibitor/antagonistmalignant breast neoplasmmicroorganismp65prototypepublic health relevancereceptorresearch studyscaffoldscreeningsmall moleculetheoriestherapeutic targettherapy developmenttooltumortumor specificity
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Regulated gene expression is essential to the normal growth and development of cells. The disruption in the network that controls this complex process is correlated with a range of human cancers. Often at the heart of these diseases are malfunctioning transcriptional activators, proteins that associate with specific genes and turn them on such that the proteins they encode are produced. This represents an opportunity to develop therapies that address transcriptional misregulation by identifying molecules that directly inhibit the function of transcriptional activators associated with breast cancer. Two complementary approaches will be used to identify small (drug-like) molecules that inhibit the function of two transcriptional activators, ESX and NF- kappaB (p50/p65 heterodimer) implicated in approximately 30% of breast cancers. Through a combination of in vitro and in vivo studies, these molecules will be assessed as individually and in combination for effectiveness in blocking growth and metastasis of ErbB2(Her2)-positive breast cancer and to provide a detailed understanding of their mechanism of action. From a broader perspective, the transcriptional inhibitors identified in this study will be outstanding tools for dissecting the relationship between misregulated transcription and breast cancer. Our study of these molecules will also be used to build a profile of what characteristics (potency, efficacy, specificity) of an effective transcriptional inhibitor should exhibit. In this way, the molecules identified here will be prototype transcription- targeted therapeutics, opening new avenues for future therapeutic investigations.
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财政年份:2002
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依托单位:
Probing Transcriptional Activation at the Molecular Level - Diversity Supplement
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资助金额:$21.14万
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依托单位:
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资助金额:$21.14万
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负责人:ANNA K. MAPP
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依托单位:
Chemical Tools for Regulating Eukaryotic Transcription
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项目类别:
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资助金额:$20.64万
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财政年份:2002
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依托单位:
Chemical Tools for Regulating Eukaryotic Transcription
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项目类别:
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资助金额:$21.14万
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财政年份:2002
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负责人:ANNA K. MAPP
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依托单位:
DESIGN OF DNA MINOR GROOVE BINDING LIGANDS
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项目类别:
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财政年份:1999
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依托单位:
DESIGN OF DNA MINOR GROOVE BINDING LIGANDS
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项目类别:
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依托单位:
海外基金