Molecular Basis of Action of the Putative Oncogene BCL-6
Molecular Basis of Action of the Putative Oncogene BCL-6
批准号:
7765615
负责人:
VIVIAN J BARDWELL
金额:
$31.11万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1996
资助国家:
美国
项目状态:
已结题
起止时间:
1996-09-30 至 2013-02-28
关键词:
AffectB-Cell LymphomasB-LymphocytesBCL6 geneBMI1 geneBiological ProcessCell Culture TechniquesCell Differentiation processCell LineCell MaintenanceCellsCentroblastClinical TrialsComplexDataDevelopmentEpigenetic ProcessEyeFingersFundingFutureGene TargetingGrantGrowthHematopoiesisHistonesHomologous GeneHumanHuman DevelopmentIn VitroLinkLymphocyteLymphomaLymphomagenesisMature B-LymphocyteMediatingMolecularMusMutationNon-Hodgkin&aposs LymphomaOncogene ProteinsOncogenesOncogenicPhenotypePlayPolycombProteinsProto-OncogenesPublic HealthRegulationRepressionRoleSiteStem cellsSyndromeTestingTranscription Repressor/CorepressorUbiquitinWorkZinc Fingersbasecardiogenesischromatin modificationcraniofacialdesignembryonic stem cellimprovedin vivolarge cell Diffuse non-Hodgkin&aposs lymphomamRNA Expressionmalemouse modelnovelpublic health relevancereconstitutiontherapeutic targetubiquitin ligaseubiquitin-protein ligase
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The proto-oncogene BCL6 encodes a POZ/BTB-zinc finger transcriptional repressor that is essential for normal lymphocyte development. When BCL6 is aberrantly expressed it leads to the development of diffuse large B cell lymphomas (DLBCL). During the last grant period we identified a novel corepressor, BCOR, which functions with BCL6. In this funding period we have shown that BCOR forms a complex with several polycomb group (PcG) proteins, including NSPC1 (a BMI1 homolog), the ubiquitin-H2A E3 ligase, RNF2, and other proteins potentially capable of further epigenetic modification of chromatin. We found that BCOR is present at multiple BCL6 target genes whose repression is likely to contribute to lymphomagenesis. Thus proteins of the BCOR complex provide candidate therapeutic targets for treatment of B cell lymphoma. We also have found that BCOR is a common insertion site in retrovirally-induced B cell lymphomas, and that these integrations cause elevated BCOR mRNA expression. This strongly suggests that BCOR acts as an oncogene. BCOR also plays a more widespread role in human development. Mutations in human BCOR cause the male-lethal X- linked Oculofaciocardiodental (OFCD) syndrome, and we showed that a hypomorphic mouse mutation in Bcor partially mimics the OFCD phenotype. Finally, inappropriate levels of BCOR and NSPC1 can disrupt ES cell differentiation, consistent with a role for the BCOR complex in stem cell maintenance or differentiation. My central hypothesis is that BCOR-mediated repression, via epigenetic mechanisms, is important for lymphomagenesis. The aims of this proposal are: first, to determine the role of BCOR in B cell lymphomagenesis both in cell culture and in vivo and second, to dissect the molecular and epigenetic mechanisms of the BCOR repression complex. The work proposed here is significant in several respects. First, BCL6 is involved in clinically important B cell lymphomas and the BCOR complex is a strong candidate to mediate BCL6 oncogenic activity. Second, our preliminary data suggest BCOR also can act as an oncogene. Third, these studies will help elucidate BCOR epigenetic repression mechanisms, which are relevant to many biological processes including eye, craniofacial, and heart development as well as hematopoiesis and lymphomagenesis. Fourth, our studies will help identify potential therapeutic targets for DLBCL. PUBLIC HEALTH RELEVANCE: The work has clear relevance to public health. BCL6 is and important oncoprotein involved in up to 50% of DLBCL, a common subtype of non-Hodgkin's lymphoma, and our data indicate that BCOR functions with BCL6. Our preliminary data suggest that BCOR also acts as an oncoprotein. Already a potential therapy based in part on work funded by this grant is nearing clinical trials, and the work proposed here should permit the design of future improved anti-lymphoma therapy.
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会议论文
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资助金额:$33.46万
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批准号:2796321
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资助金额:$10.01万
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依托单位:
MOLECULAR BASIS OF ACTION OF THE PUTATIVE ONCOGENE BCL6
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批准号:2895602
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资助金额:$10.41万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL6
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批准号:6622122
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项目类别:
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资助金额:$29.32万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL-6
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批准号:7612082
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项目类别:
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资助金额:$31.11万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
MOLECULAR BASIS OF ACTION OF THE PUTATIVE ONCOGENE BCL6
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批准号:2010067
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项目类别:
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资助金额:$9.25万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL-6
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批准号:8034680
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项目类别:
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资助金额:$30.17万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL6
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批准号:6686781
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项目类别:
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资助金额:$29.31万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL6
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批准号:6830719
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项目类别:
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资助金额:$29.31万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
MOLECULAR BASIS OF ACTION OF THE PUTATIVE ONCOGENE BCL6
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批准号:2545410
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项目类别:
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资助金额:$9.62万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
MOLECULAR BASIS OF ACTION OF THE PUTATIVE ONCOGENE BCL6
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批准号:6173431
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项目类别:
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资助金额:$10.83万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL6
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批准号:6439136
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项目类别:
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资助金额:$29.33万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL-6
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批准号:8215861
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项目类别:
-
资助金额:$30.17万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL-6
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批准号:7460374
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项目类别:
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资助金额:$31.12万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
Molecular Basis of Action of the Putative Oncogene BCL6
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批准号:6997815
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项目类别:
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资助金额:$28.62万
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财政年份:1996
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负责人:VIVIAN J BARDWELL
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依托单位:
海外基金