2012 Fiscal Year Final Research Report
Development of novel cancer therapy through the targeting bromodomain protein
Project/Area Number |
23790126
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Drug development chemistry
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Research Institution | The University of Tokyo |
Principal Investigator |
|
Project Period (FY) |
2011 – 2012
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Keywords | ゲノム創薬 |
Research Abstract |
Accumulation of BRD8 is frequently observed in colorectal cancer cells. We found that this accumulation resulted from deregulation of ubiquitin-proteasome system. Genome-wide gene expression profiling of BRD8-knocked down cells unveiled association of BRD8 with cancer progression. BRD8 may be an attractive therapeutic target for colorectal cancer.
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[Journal Article] Wnt3a stimulates maturation of impaired neutrophils developed from severe congenital neutropenia patient-derived pluripotent stem cells.2013
Author(s)
Hiramoto T, Ebihara Y, Mizoguchi Y,Nakamura K, Yamaguchi K, Ueno K, NariaiN, Mochizuki S, Yamamoto S, Nagasaki M,Furukawa Y, Tani K, Nakauchi H, KobayashiM, Tsuji K.
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Journal Title
Proc Natl Acad Sci USA.
Volume: 110(8)
Pages: 3023-3028
DOI
Peer Reviewed
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[Journal Article] MRG-binding protein contributes to colorectal cancer development.2011
Author(s)
Yamaguchi K, Sakai M, Kim J, Tsunesumi S, Fujii T, Ikenoue T, Yamada Y, Akiyama Y, Muto Y, Yamaguchi R, Miyano S, Nakamura Y, Furukawa Y.
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Journal Title
Cancer Sci.
Volume: 102(8)
Pages: 1486-1492
DOI
Peer Reviewed
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