| Project/Area Number |
11470289
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| Research Category |
Grant-in-Aid for Scientific Research (B).
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Cerebral neurosurgery
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| Research Institution | Hyogo College of Medicine |
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Principal Investigator |
NORIO Arita Hyogo College of Medicine, Neurosurgery, Professor, 医学部, 教授 (80159508)
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| Co-Investigator(Kenkyū-buntansha) |
OKANO Hideyuki Osaka University Graduate School of medicine, Neuroanatomy, Professor, 大学院・医学系研究科, 教授 (60160694)
IKEMOTO Hideyasu Hyogo College of Medicine, Neurosurgery, Assistant, 医学部, 助手 (30278824)
MATSUMOTO Tsuyoshi Hyogo College of Medicine, Neurosurgery, Associate Professor, 医学部, 講師 (00181777)
藤川 浩一 兵庫医科大学, 医学部, 助手 (40312136)
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| Project Period (FY) |
1999 – 2000
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| Project Status |
Completed (Fiscal Year 2000)
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| Budget Amount *help |
¥14,600,000 (Direct Cost: ¥14,600,000)
Fiscal Year 2000: ¥5,100,000 (Direct Cost: ¥5,100,000)
Fiscal Year 1999: ¥9,500,000 (Direct Cost: ¥9,500,000)
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| Keywords | neural stem cell / MSI1 / glioma / glioblastoma / astrocytoma / oligodendroglioma / GFAP / Hu / ependymona / central neurocytoma |
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| Research Abstract |
Tumor cells often express phenotypic markers that are specific to the cells from which they originated. A neural RNA-binding protein, Musashil, is an evolutionarily well-conserved marker for neural stem cells/progenitor cells. To examine the origin of gliomas, we examined the expression of the human Musashil homolog, MSI1, in human glioma tissues and in normal human adult and fetal brains. As we had seen previously in rodents, in the normal human brain, MSI1 was expressed in cells located in the ventricular and subventricular zones, in GFAP-negative glial cells, and in GFAP-positive astrocytes. In glioblastomas, MSI1 was expressed in GFAP-negative tumor cells forming foci that were clearly demarcated and surrounded by GFAP-positive cells. Tumor cells arranged in pseudopalisades were also strongly immunoreactive with MSI1 antibodies. The percentage of MSI1-labeled tumor cells increased in higher-grade astrocytomas and correlated with proliferative activity, as estimated by an MIB-1 staining index. Our results indicate MSI1 is an excellent marker for neural progenitor cells including neural stem cells in normal human brains. Furthermore, the expression of MSI1 correlates well with the immature nature as well as the malignancy of tumor cells in human gliomas. Thus, we expect the analysis of MSI1 expression to contribute to the understanding of the cellular origin and biology of human gliomas.
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