2010 Fiscal Year Final Research Report
Roles ofAML1 mutants in the development of myelodysplastic syndromes
Project/Area Number |
20599009
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Hematology
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Research Institution | Osaka University |
Principal Investigator |
SATOH Yusuke Osaka University, 医学系研究科, 助教 (20506307)
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Co-Investigator(Kenkyū-buntansha) |
KANAKURA Yuzuru 大阪大学, 医学系研究科, 助教 (20177489)
YOKOTA Takafumi 大阪大学, 医学系研究科, 助教 (60403200)
MAEDA Tetsuo 大阪大学, 医学系研究科, 助教 (00403064)
MATSUMURA Itaru 大阪大学, 医学系研究科, 准教授 (00294083)
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Project Period (FY) |
2008 – 2010
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Keywords | 骨髄異形成症候群 / 急性骨髄性白血病 / AML1 / RUNX1 / DNA修復 |
Research Abstract |
We performed the functional analysis of AML1dC, which is a dominant negative mutant of AML1. As a result, we found that AML1dC enhances proliferating ability of hematopoietic stem/progenitor cells (HSPC ) and attenuates DNA repair ability of HSPC. Through these mechanisms, AML1dC promotes the development of myelodysplastic syndromes (MDS) and the transition from MDS to acute myeloid leukemia.
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Research Products
(15 results)
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[Journal Article] BCR-ABL but not JAK2 V617F inhibits erythropoiesis through the Ras signal by inducing p21CIP1/WAF1.2010
Author(s)
Tokunaga M, Ezoe S, Tanaka H, Satoh Y, Fukushima K, Matsui K, Shibata M, Tanimura A, Oritani K, Matsumura I, Kanakura Y.
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Journal Title
J.Biol.Chem. 285
Pages: 31774-31782
Peer Reviewed
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[Journal Article] AML1/RUNX1 Works as a Negative Regulator of c-Mpl in Hematopoietic Stem Cells.2008
Author(s)
Satoh Y, Matsumura I, Tanaka H, Ezoe S, Fukushima K, Tokunaga M, Yasumi M, Shibayama H, Mizuki M, Era T, Okuda T, Kanakura Y.
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Journal Title
J.Biol.Chem. 283
Pages: 30045-30056
Peer Reviewed
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[Journal Article] Predictability of the response to tyrosine kinase inhibitors via in vitro analysis of Ber-Abl phosphorylation.
Author(s)
Shibata M, Ezoe S, Oritani K, Matsui K, Tokunaga M, Fujita N, Saito Y, Takahashi T, Hino M, Matsumura I, Kanakura Y.
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Journal Title
Peer Reviewed
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