| Project/Area Number |
26670857
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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 |
Surgical dentistry
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| Research Institution | Chiba University |
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Principal Investigator |
HIDEKI TANZAWA 千葉大学, 医学(系)研究科(研究院), 教授 (50236775)
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| Co-Investigator(Kenkyū-buntansha) |
KASAMATSU ATSUSHI 千葉大学, 医学部付属病院, 講師 (60375730)
HIGO MORIHIRO 千葉大学, 医学部付属病院, 助教 (60724383)
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| Project Period (FY) |
2014-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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| Keywords | KIF4A / 口腔扁平上皮癌 / タキサン系抗癌剤 / 微小管作動性制御 / kinesin family（KIF） |
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| Outline of Final Research Achievements |
In this study, the resistant mechanism to taxane-based anticancer drug was analyzed. Our preliminary study has already revealed that the specific enhanced expression of KIF family genes, which act to microtubules, was confirmed in oral squamous cell carcinomas (OSCCs). Of KIF family genes, we focused on KIF4A because of its expression pattern. In both in vitro and in vivo, the transformation experiments using shRNA indicated the involvement of KIF4A in resistance to taxane, anti-cancer drug. Because KIF genes are involved in the separation of chromosomes and the arrangement of the spindle, cytokinesis through the microtubule, we also reconfirmed the role of KIF4A controlling the expression status of the spindle assembly checkpoint (SAC)- -related molecules (BUB1, MAD2, CDC20, and cyclin B1).
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