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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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DOI: 10.1038/srep18388
发表时间: 2015-12-21
期刊: Scientific reports
影响因子: 4.6
作者: [Oliviero G, Munawar N, Watson A, Streubel G, Manning G, Bardwell V, Bracken AP, Cagney G]
通讯作者: Cagney G
Bcor insufficiency promotes initiation and progression of myelodysplastic syndrome.
Bcor 不足会促进骨髓增生异常综合征的发生和进展。
DOI: 10.1182/blood-2018-01-827964
发表时间: 2018
期刊: Blood
影响因子: 20.3
作者: [Tara S, Isshiki Y, Nakajima-Takagi Y, Oshima M, Aoyama K, Tanaka T, Shinoda D, Koide S, Saraya A, Miyagi S, Manabe I, Matsui H, Koseki H, Bardwell VJ, Iwama A.]
通讯作者: Iwama A.
DOI: 10.1038/ncomms14581
发表时间: 2017-03-06
期刊: Nature communications
影响因子: 16.6
作者: [Lefebure M, Tothill RW, Kruse E, Hawkins ED, Shortt J, Matthews GM, Gregory GP, Martin BP, Kelly MJ, Todorovski I, Doyle MA, Lupat R, Li J, Schroeder J, Wall M, Craig S, Poortinga G, Cameron D, Bywater M, Kats L, Gearhart MD, Bardwell VJ, Dickins RA, Hannan RD, Papenfuss AT, Johnstone RW]
通讯作者: Johnstone RW
DOI: 10.1016/j.celrep.2013.06.016
发表时间: 2013-08-15
期刊: Cell reports
影响因子: 8.8
作者: [Hatzi K, Jiang Y, Huang C, Garrett-Bakelman F, Gearhart MD, Giannopoulou EG, Zumbo P, Kirouac K, Bhaskara S, Polo JM, Kormaksson M, MacKerell AD Jr, Xue F, Mason CE, Hiebert SW, Prive GG, Cerchietti L, Bardwell VJ, Elemento O, Melnick A]
通讯作者: Melnick A
Control of Trophoblast Differentiation in Placental Development
  • 批准号:
    9309015
  • 项目类别:
  • 资助金额:
    $33.46万
  • 财政年份:
    2016
  • 负责人:
    VIVIAN J BARDWELL
  • 依托单位:
Control of Trophoblast Differentiation in Placental Development
  • 批准号:
    9922711
  • 项目类别:
  • 资助金额:
    $33.04万
  • 财政年份:
    2016
  • 负责人:
    VIVIAN J BARDWELL
  • 依托单位:
DMRT1 in Mammalian Sexual Development
  • 批准号:
    9026212
  • 项目类别:
  • 资助金额:
    $60.87万
  • 财政年份:
    1999
  • 负责人:
    VIVIAN J BARDWELL
  • 依托单位:
MOLECULAR BASIS OF ACTION OF THE PUTATIVE ONCOGENE BCL6
  • 批准号:
    2796321
  • 项目类别:
  • 资助金额:
    $10.01万
  • 财政年份:
    1996
  • 负责人:
    VIVIAN J BARDWELL
  • 依托单位:
海外基金