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F-box proteins: deregulated cell cycle control and proteolysis in cancer

F-box proteins: deregulated cell cycle control and proteolysis in cancer
F-box 蛋白:癌症中细胞周期控制和蛋白水解失调
批准号:
8676437
负责人:
MICHELE PAGANO
金额:
$44.65万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-07-01 至 2015-11-30
关键词:
AffectAnimal ModelAreaBasic ScienceBiochemicalBiologicalBreastBreast Cancer cell lineBreast CarcinomaBreast LymphomaCancer BiologyCancer PatientCell CycleCell Cycle ProgressionCell Cycle RegulationCell ProliferationCell SurvivalCell divisionCell physiologyCellsCellular biologyCircadian RhythmsClock proteinDataDatabasesDevelopmentDimensionsDominant-Negative MutationDown-RegulationElementsEnsureEpithelialEpitheliumEstrogen ReceptorsEventF-Box ProteinsFailureFamilyFundingGenesGeneticGenetic TranscriptionGoalsGrowthGrowth and Development functionHumanHuman PathologyInstructionKnowledgeLaboratoriesLeadLifeLigaseLymphoidLymphomaMalignant - descriptorMalignant NeoplasmsMalignant neoplasm of prostateManuscriptsMediatingMethodsMicroarray AnalysisMolecularMusMutant Strains MiceMutationNormal tissue morphologyOncogene ProteinsOrganOutcomePathway interactionsPlayPreparationProcessPrognostic MarkerProteasome InhibitorProteinsProteolysisProto-OncogenesPublicationsRegulationRelative (related person)ResearchRoleS PhaseSamplingSignal TransductionSolidSomatic CellSomatic Cell GeneticsSystemTherapeuticTherapeutic InterventionTimeTissuesTransgenic MiceTranslational ResearchTumor BankTumor Cell LineTumor Suppressor GenesTumor Suppressor ProteinsUbiquitinUbiquitin-mediated Proteolysis PathwayUnited States National Institutes of HealthWorkbasecell growthcell transformationcircadian pacemakercyclin Fgenetic regulatory proteinhydroxyureain vivoinhibitor/antagonistinterdisciplinary approachmalignant breast neoplasmmammary epitheliummouse modelmultidisciplinarymutantneoplasticnoveloverexpressionpreclinical studyprognostic valueprogramssmall moleculesuccesstargeted cancer therapytissue culturetooltumortumorigenesisubiquitin ligase

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英文摘要
A detailed understanding of the molecular and cellular events influencing the three key dimensions of cellular life (growth/proliferation, survival, and differentiation) remains a central question in cancer biology. Further understanding of the influence of the ubiquitin system on the transformation process will help to identify novel targets for cancer therapy. The first years of work under CA76584 (started in 1998) set the bases for elucidating the role played by F-box proteins in human oncogenesis, which was accomplished during the second funding cycle. In its third cycle, CA76584 is currently devoted to elucidating the integration of the ubiquitin system in the signaling networks of the cell, and its corruption in cancer. In particular, our research program involves the study of the human family of SCF and SCF-like ubiquitin ligases to gain an understanding of the molecular mechanisms through which they control basic cellular processes, such as cell growth, cell division, and cell survival. To this end, we are using a comprehensive and interdisciplinary approach that includes biochemical and biological methods, as well as somatic cell and mouse genetics. These tools, together with our expertise in the ubiquitin system, will ensure that our laboratory will continue to contribute to the understanding of cell functions during the coming years. As the mechanisms of the ubiquitin-mediated proteolysis of cell cycle regulators are unraveled, this team is committed to the integration of its basic research results with an understanding of malignant transformation.
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