Hematopoietic specific Genes in Stem Cell Development
Hematopoietic specific Genes in Stem Cell Development
批准号:
7385143
负责人:
BING LIM
金额:
$33.41万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-05-10 至 2009-08-28
关键词:
4p13AdhesionsAffectAntineoplastic AgentsApoptosisAppendixCell ShapeCell divisionCell physiologyCellsChimeric ProteinsChromosomesClassClinicalCytoskeletal ModelingDevelopmentDiffuse LymphomaFamilyFrequenciesGenesGenetic TranscriptionHematologic NeoplasmsHematopoiesisHematopoieticHematopoietic NeoplasmsIntegrinsInvestigationKnowledgeLaboratoriesLymphocyteLymphomaLymphomagenesisManuscriptsMediatingMonomeric GTP-Binding ProteinsMultiple MyelomaMutationNamesNeoplasm MetastasisOutcomePlayProtein FamilyProteinsRoleStem Cell DevelopmentT-Lymphocytebasecarcinogenesisdrug developmentgenetic regulatory proteininhibitor/antagonistinterestknock-downlarge cell Diffuse non-Hodgkin&aposs lymphomamembermetaplastic cell transformationrhotraffickingtumor progression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This is a proposal to continue the investigation of the role of RhoGTPases and their regulatory proteins in hematopoiesis, hematopoietic cell function and hematopoietic malignancies. The RhoGTPases form a large family of proteins that mediate an extensive array of fundamental cellular function including cell division, cell shape, intra-cellular trafficking, cytoskeletal organization, gene transcription, apoptosis, cellular transformation and metastasis. Recently a new member of the RhoGTPase family have been discovered named RhoH, that is expressed specifically only in hematopoietic cells. RhoH was first identified as a fusion protein with bcl6 in non-random translocations involving the RhoH gene at chromosome 4p13 in some cases of lyrnphoma and myeloma. Even more significant is the recent finding that a high frequency of RhoH mutations exist in the Diffuse Large B-Cell Lymphomas (DLCL). This is the first example of the involvement of a RhoGTPase in hematological malignancies, and the clinical importance of the Rho family of proteins. The pathological role of these mutations remain to be clarified. Important clues derived from recent surprising finding showed that RhoH functions as a potent inhibitor of other RhoGTPases. Consistent with RhoH being an "inhibitory" protein is the recent discovery that a cellular basal level of RhoH is crucial for maintaining T cells in the non-adherant inactive state. RhoH represents a new paradigm for the functional modulation of the RhoGTPases and other related small G-proteins. An important question is what does RhoH do, why does it function differently compared to other RhoGTPases and what is RhoH role in lymphomagenesis? We shall focus our effort to answer the following questions:Aim1) What is the cellular function of RhoH? ; Aim2) What is the mechanism of RhoH inhibitory function?; Aim3) What are the consequences of RhoH mutations in lymphoma? Knowledge from this project will bring new insigths about an important class of proteins that are increasingly implicated in carcinogenesis and cancer progression. The study will also allow us to determine if RhoH is a meaningful variable for prognostication in sub-groups of DLCL and if it can be a useful target for anti-cancer drug development.
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RhoGTPases and their role in cancer.
RhoGTPases 及其在癌症中的作用。
DOI:
10.3727/096504003108748528
发表时间:
2003
期刊:
Oncology research
影响因子:
3.1
作者:
[Li,Xiaoyu, Lim,Bing]
通讯作者:
Lim,Bing
Reconstitution of mammary epithelial morphogenesis by murine embryonic stem cells undergoing hematopoietic stem cell differentiation.
鼠类胚胎干细胞经历造血干细胞分化的乳腺上皮形态发生。
DOI:
10.1371/journal.pone.0009707
发表时间:
2010-03-15
期刊:
PLOS ONE
影响因子:
3.7
作者:
[Jiang, Shuxian, Lee, Byeong-Chel, Fu, Yigong, Avraham, Shalom, Lim, Bing, Avraham, Hava Karsenty]
通讯作者:
Avraham, Hava Karsenty
DOI:
10.1182/blood.v88.7.2722.bloodjournal8872722
发表时间:
1996-10-01
期刊:
BLOOD
影响因子:
20.3
作者:
[Guillemot, JC, Kruskal, BA, Lim, B]
通讯作者:
Lim, B
cDNA cloning and functional characterization of the mouse Ca2+-gated K+ channel, mIK1. Roles in regulatory volume decrease and erythroid differentiation.
小鼠 Ca2 门控 K 通道 mIK1 的 cDNA 克隆和功能表征。
DOI:
10.1074/jbc.273.34.21542
发表时间:
1998
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Vandorpe,DH, Shmukler,BE, Jiang,L, Lim,B, Maylie,J, Adelman,JP, deFranceschi,L, Cappellini,MD, Brugnara,C, Alper,SL]
通讯作者:
Alper,SL
DOI:
10.1038/nature08735
发表时间:
2010-02-25
期刊:
Nature
影响因子:
64.8
作者:
[]
通讯作者:
共 9 条
Development of a stem-cell derived thymic cell therapy to treat patients with athymia
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批准号:10609940
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项目类别:
-
资助金额:$28.67万
-
财政年份:2022
-
负责人:BING LIM
-
依托单位:
Development of a stem-cell derived thymic cell therapy to treat patients with athymia
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批准号:10483294
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项目类别:
-
资助金额:$30.0万
-
财政年份:2022
-
负责人:BING LIM
-
依托单位:
CHARACTERIZATION OF A NEW MOUSE MODEL FOR LUPUS
-
批准号:6835641
-
项目类别:
-
资助金额:$33.37万
-
财政年份:2003
-
负责人:BING LIM
-
依托单位:
CHARACTERIZATION OF A NEW MOUSE MODEL FOR LUPUS
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批准号:6605150
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项目类别:
-
资助金额:$11.71万
-
财政年份:2003
-
负责人:BING LIM
-
依托单位:
CHARACTERIZATION OF A NEW MOUSE MODEL FOR LUPUS
-
批准号:7009894
-
项目类别:
-
资助金额:$32.59万
-
财政年份:2003
-
负责人:BING LIM
-
依托单位:
CHARACTERIZATION OF A NEW MOUSE MODEL FOR LUPUS
-
批准号:6802260
-
项目类别:
-
资助金额:$33.37万
-
财政年份:2003
-
负责人:BING LIM
-
依托单位:
CHARACTERIZATION OF A NEW MOUSE MODEL FOR LUPUS
-
批准号:7163025
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项目类别:
-
资助金额:$31.64万
-
财政年份:2003
-
负责人:BING LIM
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依托单位:
LYSOSOMAL PROTEOLYSIS IN HEMATOPOIETIC CELLS
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批准号:2684379
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项目类别:
-
资助金额:$24.9万
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财政年份:1998
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负责人:BING LIM
-
依托单位:
LYSOSOMAL PROTEOLYSIS IN HEMATOPOIETIC CELLS
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批准号:6381219
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项目类别:
-
资助金额:$27.21万
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财政年份:1998
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负责人:BING LIM
-
依托单位:
LYSOSOMAL PROTEOLYSIS IN HEMATOPOIETIC CELLS
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批准号:2906281
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项目类别:
-
资助金额:$25.64万
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财政年份:1998
-
负责人:BING LIM
-
依托单位:
LYSOSOMAL PROTEOLYSIS IN HEMATOPOIETIC CELLS
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批准号:6177934
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项目类别:
-
资助金额:$26.41万
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财政年份:1998
-
负责人:BING LIM
-
依托单位:
Hematopoietic specific Genes in Stem Cell Development
-
批准号:7031529
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项目类别:
-
资助金额:$35.11万
-
财政年份:1995
-
负责人:BING LIM
-
依托单位:
HEMATOPOIETIC SPECIFIC GENES IN STEM CELL DEVELOPMENT
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批准号:2414859
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项目类别:
-
资助金额:$23.01万
-
财政年份:1995
-
负责人:BING LIM
-
依托单位:
HEMATOPOIETIC SPECIFIC GENES IN STEM CELL DEVELOPMENT
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批准号:2147403
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项目类别:
-
资助金额:$21.19万
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财政年份:1995
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负责人:BING LIM
-
依托单位:
HEMATOPOIETIC SPECIFIC GENES IN STEM CELL DEVELOPMENT
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批准号:2147404
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项目类别:
-
资助金额:$22.13万
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财政年份:1995
-
负责人:BING LIM
-
依托单位:
HEMATOPOIETIC SPECIFIC GENES IN STEM CELL DEVELOPMENT
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批准号:6177047
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项目类别:
-
资助金额:$29.97万
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财政年份:1995
-
负责人:BING LIM
-
依托单位:
Hematopoietic specific Genes in Stem Cell Development
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批准号:7208949
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项目类别:
-
资助金额:$34.09万
-
财政年份:1995
-
负责人:BING LIM
-
依托单位:
Hematopoietic specific Genes in Stem Cell Development
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批准号:6862570
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项目类别:
-
资助金额:$35.96万
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财政年份:1995
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负责人:BING LIM
-
依托单位:
HEMATOPOIETIC SPECIFIC GENES IN STEM CELL DEVELOPMENT
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批准号:6380855
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项目类别:
-
资助金额:$30.87万
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财政年份:1995
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负责人:BING LIM
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依托单位:
Hematopoietic specific Genes in Stem Cell Development
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批准号:6726631
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项目类别:
-
资助金额:$35.96万
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财政年份:1995
-
负责人:BING LIM
-
依托单位:
海外基金