Oncogenic programs driven by notch signaling in B-cell lymphoma
Oncogenic programs driven by notch signaling in B-cell lymphoma
批准号:
9751805
负责人:
RUSSELL James Hubbard RYAN
金额:
$16.56万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-01 至 2021-08-31
关键词:
Academic Medical CentersAcetylationAdvisory CommitteesAnatomyAntibodiesAreaAwardB-Cell LymphomasBiologicalBiologyBiomedical ResearchBlood CellsCell LineCell ProliferationCell SurvivalCellsCessation of lifeChronic Lymphocytic LeukemiaClinicalClinical TreatmentClustered Regularly Interspaced Short Palindromic RepeatsCollaborationsCommunication ResearchComplexDNA Sequence RearrangementDana-Farber Cancer InstituteDataData SetDevelopmentDevelopment PlansDiagnosticDiseaseDistalDrug SynergismEducational process of instructingElementsEnhancersFlow CytometryGene ActivationGene Expression ProfilingGene MutationGene TargetingGeneral HospitalsGenesGenetic RiskGenetic TranscriptionGrantHematologic NeoplasmsHeterogeneityHistone AcetylationHospitalsHumanImageImmobilizationImmunohistochemistryIn VitroInstitutesInstitutionInternationalInvestigationInvestigational TherapiesKnock-outLaboratoriesLaboratory ResearchLarge-Cell LymphomasLeadLeadershipLesionLigandsLinkLymphocyteLymphomaMalignant NeoplasmsMalignant lymphoid neoplasmMantle Cell LymphomaMassachusettsMediatingMentorsMentorshipModelingMolecularMutationNOTCH1 geneNotch Signaling PathwayNuclearOncogenesOncogenicOutcomePathologyPathway interactionsPatient-Focused OutcomesPatientsPhysiciansPhysiologicalPlayPositioning AttributePreclinical TestingPrimary NeoplasmPrincipal InvestigatorProfessional CompetenceReceptors, Antigen, B-CellRecombinantsRecording of previous eventsRecurrenceRefractory DiseaseRegulator GenesRegulatory ElementResearchResearch PersonnelResearch ProposalsResearch TrainingResourcesRoleSamplingScientistSignal TransductionSmall-Cell LymphomaSorting - Cell MovementSpecimenStromal CellsStructureStudy modelsSubgroupSupporting CellTherapeuticTherapeutic Human ExperimentationTimeTissuesTrainingTranscriptional RegulationTransgenesUniversitiesWomanWritingXenograft ModelXenograft procedurebasecancer cellcancer diagnosiscareercareer developmentcell growthchronic lymphocytic leukemia cellclinical Diagnosisdesignepigenetic profilingepigenetic regulationexperienceexperimental studygain of function mutationgamma secretasegenome-widegenome-wide analysishigh riskimprovedin vitro Modelin vivoin vivo Modelinhibitor/antagonistinsightinterestlymph nodesmolecular diagnosticsmolecular markermouse modelneoplastic cellnotch proteinnovel strategiesnovel therapeutic interventionoverexpressionperipheral bloodprogramsresponsesingle cell analysissingle-cell RNA sequencingskillstenure tracktooltranscription factortreatment strategytumortumor growth
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英文摘要
PROJECT SUMMARY / ABSTRACT
Despite advances in the clinical treatment of B-cell lymphoma, patients with certain high-risk genetic lesions
continue to have poor outcomes with current therapies. Recurrent gain-of-function mutations in genes
encoding Notch receptors are associated with aggressive disease and decreased survival in chronic
lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL). The oncogenic effects of altered Notch
signaling are likely mediated through activation of gene regulatory targets by the Notch transcription factor
complex, but the specific targets of altered Notch signaling in B-cell lymphoma are largely unknown, limiting
our ability to devise rational treatment strategies for these patients. I recently used genome-wide epigenetic
profiling to identify lymphoma subtype-specific enhancers and enhancer-associated genomic rearrangements
in primary tumor samples from diverse B-cell lymphoma subtypes (Cancer Discovery, 2015), linking
transcription factor-mediated enhancer activation to specific oncogene programs. I will extend this approach in
primary CLL and MCL specimens, as well as physiologically relevant in vitro and in vivo models, to uncover the
specific gene targets of Notch signaling and identify cooperating pathways. I will use this improved biological
understanding of the role of Notch in B-cell lymphomas to design and pre-clinically test novel strategies for the
treatment of Notch-driven lymphomas.
I am a hematopathologist with a strong research interest in the role of altered transcriptional regulatory genes
in the biology of B-cell lymphoma. My primary career objective in the coming years is to obtain a tenure-track
position at an academic medical center as a research laboratory Principal Investigator. I am seeking K08
support for mentored research in the laboratory of Dr. Bradley Bernstein at Massachusetts General Hospital /
Broad Institute, with co-mentorship from Dr. Jon Aster at Brigham and Women’s Hospital and Dana-Farber
Cancer Institute. A K08 award would give me protected time to advance my research program, to develop
additional skills in the biological analysis of genome-wide data sets, and to pursue specialized training and
experience in the use of physiologically relevant mouse models for the study of lymphoma. I will devote at least
80% of my time to a focused research investigation into the mechanisms of Notch signaling and transcriptional
regulation in B cell lymphomas, with up to 20% of my time devoted to the clinical diagnosis of hematological
malignancies, as well as teaching and training pursuits. Massachusetts General Hospital, Broad Institute of
MIT and Harvard University, Brigham and Women’s Hospital, and Dana-Farber Cancer Institute are institutions
of international renown in the fields of biomedical research and research training, and host the laboratories of
many highly accomplished experts in lymphoid malignancy, transcriptional and epigenetic regulation, and
experimental therapeutics. The Department of Pathology at Massachusetts General Hospital has a
distinguished history in the training of independent cancer researchers, and the development and use of
advanced molecular tools for cancer diagnosis. I have assembled an advisory team of local experts in areas of
importance to my project, consisting of Dr. Catherine Wu, Dr. X. Shirley Liu, and Dr. David Weinstock, who will
advise me in the conduct of this research, as well as my career development. I have initiated collaborations
with other academic physicians and scientists who will provide specific resources and guidance to advance my
investigations (Dr. Irwin Bernstein, in vitro modeling of Notch activation, Dr. A. John Iafrate, molecular
diagnostics and biomarkers, and Dr. Ephraim Hochberg, clinical therapeutic research in lymphoma). I have
formulated a structured career development plan that includes training and mentorship in laboratory
management, scientific leadership, research communication, grant writing, and other critical career skills.
Together, the elements of this proposal will provide me with the experience, training, and mentorship needed
to become a successful independent physician-scientist with a clinical focus on lymphoma diagnostics, and a
productive research career in basic and translational lymphoma biology.
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会议论文
Identifying Functional Drivers of MYC Activation via Developmental Enhancers in Diffuse Large B-cell Lymphoma
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批准号:10412020
-
项目类别:
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资助金额:$35.33万
-
财政年份:2020
-
负责人:RUSSELL James Hubbard RYAN
-
依托单位:
Identifying Functional Drivers of MYC Activation via Developmental Enhancers in Diffuse Large B-cell Lymphoma
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批准号:10207556
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项目类别:
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资助金额:$35.34万
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财政年份:2020
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负责人:RUSSELL James Hubbard RYAN
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依托单位:
Identifying Functional Drivers of MYC Activation via Developmental Enhancers in Diffuse Large B-cell Lymphoma
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批准号:10654743
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项目类别:
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资助金额:$34.62万
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财政年份:2020
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负责人:RUSSELL James Hubbard RYAN
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依托单位:
Oncogenic programs driven by Notch signaling in B-cell lymphoma
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批准号:9164788
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项目类别:
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资助金额:$18.04万
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财政年份:2016
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负责人:RUSSELL James Hubbard RYAN
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依托单位:
海外基金