2017 Fiscal Year Final Research Report
Factors of radioresistance for oral cancer cells which were treated with KPU-300 radiosensitizing therapy.
Project/Area Number |
16H07076
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Surgical dentistry
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Research Institution | Nagasaki University |
Principal Investigator |
OKUYAMA Kohei 長崎大学, 病院(歯学系), 助教 (30781968)
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Research Collaborator |
SUZUKI Keiji 長崎大学, 原爆後障害医療研究所, 准教授 (00196809)
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Project Period (FY) |
2016-08-26 – 2018-03-31
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Keywords | Fucci / 舌癌 / 細胞周期 / 放射線増感 / 微小管重合阻害 / M期 / KPU-300 |
Outline of Final Research Achievements |
KPU-300 is a novel colchicine-type anti-microtubule agent derived from pulinabulin (NPI-2358). We characterized the effects of KPU-300 on cell cycle kinetics and radiosensitization using SAS cells, oral tongue cancer cell line, expressing the fluorescent ubiquitination-based cell cycle indicator (Fucci). KPU-300 was reported as a potent radiosensitizer which is due to the synchronization of cells in M phase. However, SAS-Fucci cells did not do that; cells tend to be arrested in G1 phase and dead cells were gathered with the center of colony.
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Free Research Field |
口腔がん
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