| Project/Area Number |
25462256
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Neurosurgery
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| Research Institution | Research Institute, Osaka Medical Center for Cancer and Cardiovascular Disaeses |
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Principal Investigator |
KINOSHITA MANABU 地方独立行政法人大阪府立病院機構大阪府立成人病センター(研究所), 脳神経外科, 医長 (40448064)
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| Co-Investigator(Kenkyū-buntansha) |
YOSHIOKA Yoshichika 大阪大学, 免疫学フロンティア研究センター, 特任教授(常勤) (00174897)
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| Project Period (FY) |
2013-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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| Keywords | MRI / 膠芽腫 / 細胞浸潤 / in vivo イメージング / 分子イメージング |
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| Outline of Final Research Achievements |
A promising MR reporter gene, MagA was used to attempt microglia imaging in glioblastoma in a murine brain tumor model. A chimera MagA transgenic mouse was successfully established and a glioblastoma brain tumor model was produced by implanting murine glioblastoma cells into the brain. Detection of microglia, or any MagA positive cells, however, on MRI was unsuccessful. Taking into account new data published from other institutions, it is speculated that cell toxicity of MagA in murine cell lines interfered with the expression level of MagA within the cells that was targeted to be reported on MRI. On the other hand, our research was able to develop novel image analyzing techniques to identify the tumor heterogeneity and tumor boarder diffuseness using MRI, which characteristics reflect tumor cell biology of gliomas.
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