Regulation of c-myc translation by hnRNP A1: role in multiple myeloma tumor respo
Regulation of c-myc translation by hnRNP A1: role in multiple myeloma tumor respo
批准号:
8509516
负责人:
JOSEPH F GERA
金额:
$24.91万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2015-05-31
关键词:
5&apos Untranslated RegionsAddressAffectBindingBiological AssayCell LineCell NucleusCell ProliferationCell physiologyCellsClinicalComplexCytoplasmDataDevelopmentDown-RegulationEventFutureG1 ArrestGenetic TranscriptionGoalsGrowthGrowth FactorHealthInterleukin-6Internal Ribosome Entry SiteMAP Kinase GeneMAPK14 geneMaintenanceMalignant NeoplasmsMediatingMediator of activation proteinMessenger RNAMinorityMitogen-Activated Protein Kinase InhibitorMolecularMolecular ConformationMonoclonal gammopathy of uncertain significanceMultiple MyelomaNewly DiagnosedNuclearParalysedPathway interactionsPatientsPhosphorylationPhosphotransferasesPoint MutationPremalignantPrimary NeoplasmProtein BindingProteinsProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-mycRNARNA annealingRNA-Binding ProteinsRegulationResearchResistanceRibosomesRoleSamplingScientistSerineSignal PathwaySirolimusSiteStructureSyndromeTalentsTestingTherapeuticTherapeutic AgentsTranscriptTranslatingTranslationsTransport ProcessUp-RegulationXenograft Modelc-myc Genescancer cellfallsfollow-uphnRNP A1in vivoinsightmRNA StabilitymTOR InhibitormTOR inhibitionneoplastic cellnovel therapeuticspre-clinicalpreventprotein expressionresponsetraffickingtranslation factortumortumor growthtumor xenograft
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The long range goal of the proposal is to investigate the mechanism of cap-independent translation of the c-myc protein with the assumption that its cellular function is a key determinant of tumor cell responses, especially for the malignancy multiple myeloma. More specifically, the proposal will elucidate how hnRNP A1 (A1) functions as a trans-acting protein that binds to the internal ribosome entry site (IRES) in the 5' UTR of the c-myc transcript, thus facilitating IRES-dependent translation of myc. Furthermore, it will focus on the ability of Akt and MAPK cascades to regulate this A1 translation-promoting activity, testing effects on the IRES-annealing activity of A1, effects on IRES-ribosome binding and effects on A1/IRES subcellular localization. Multiple myeloma cell lines, primary tumor cells and xenograft models will be used to exploit the insight gained on A1/myc IRES regulatory controls to understand mechanisms of myeloma progression due to IL-6 stimulation and myeloma therapy-resistance when treatment with mTOR inhibitors is attempted.
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海外基金