Clarification of proliferation and deveropment mechanism as the targetting cytokine in oral cancer
| Project/Area Number |
23592974
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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 |
Surgical dentistry
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| Research Institution | Meikai University |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
OHMORI Yoshihiro 明海大学, 歯学部, 教授 (50194311)
FUKUDA Masakatsu 明海大学, 歯学部, 講師 (10311614)
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| Project Period (FY) |
2011 – 2013
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | 口腔癌 / サイトカイン / p53 / IL-23 / TNF-α / アポトーシス / NF-κB |
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| Research Abstract |
IL-23 was constitutively expressed in oral cancer cells. The up-regulation of IL-23 expression was observed, especially in p53 mutant cells. In contrast, the reduced expression of IL-23 was observed in SAS cells of p53 wild type. p53 knockdown in SAS cells led to increase IL-23 mRNA expression. However, there was no significant difference in IL-23 protein level in the transfected-control siRNA cells. Then, when the p53 knockdowned-SAS cells were stimulated with TNF-alpha, a time-dependent increase in the IL-23 protein expression was observed. These data indicate a possibility that IL-23 expression is regulated by p53. In addition, the localization of p53 and IL-23 in the biopsy samples of oral cancer was examined using an immunohistochemical method. The positive reaction for IL-23 was observed in 10 of 22 (p53 positive) cases (45.5%) of SCC. These data suggest that p53 gene alteration leads the growth and proliferation of oral cancer by the enhanced IL-23 expression.
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Report
(4 results)
Research Products
(20 results)
