2011 Fiscal Year Final Research Report
Analysis of pathogenesis of juvenile myelomonocytic leukemia and establishment of its treatment using disease-specific iPS cells
| Project/Area Number |
23659514
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Pediatrics
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| Research Institution | The University of Tokyo |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
ETO Kouji 京都大学, iPS細胞研究所, 教授 (50286986)
MOCHIZUKI Shinji 東京大学, 医科学研究所, 特任助教 (90349473)
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| Project Period (FY) |
2011
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| Keywords | 若年性骨髄単球性白血病 / iPS細胞 / 1型神経線維腫症 / NF1 |
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| Research Abstract |
To clarify the mechanisms in which the continuous activation of GM-CSF receptor-RAS pathway induces juvenile myelomonocytoc leukemia(JMML), we tried to establish induced pluripotent stem cells derived from patients with type 1 neurofibromatosis(NF1-iPS cells) possessing a heterozygous mutation of NF1. However, NF1-iPS cells were not established in spite of several times of transduction experiments., We are now using Sendai virus vectors for the transduction of various reprogramming factors into somatic cells of NF1 patients, but our result may suggest a possibility that NF1 mutation may suppress the nuclear reprogramming.
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Research Products
(49 results)
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[Book] 細胞2011
Author(s)
遠藤大, 他
Total Pages
367-370
Publisher
ニューサイエンス社
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