Elucidation of pro-metastatic property of interferon degradation
| Project/Area Number |
25670841
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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 | Tsurumi University (2014)
Tohoku University (2013) |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
SHINOHARA Fumiaki 東北大学, 歯学研究科, 非常勤講師 (80400258)
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| Project Period (FY) |
2013-04-01 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2013: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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| Keywords | インターフェロン / 腫瘍免疫 / サイトカイン / 破骨細胞 / ADAM１７ / TACE / インターフェロンγ / ADAM17 / NK細胞 / インターフェロンガンマ / 腫瘍細胞 / ADAM |
|---|
| Outline of Final Research Achievements |
ADAM family enzymes, which are highly expressed in cancer cells, were reported as the prognostic factor of tumor. In addition, some cancer cells favor to metastasize into bone marrow through the induction of osteoclastic bone resorption around cancer cells.
In the present study, we investigated the degradation mechanism of interferon gamma, which shows anti-osteoclastogenic and anti-tumorigenic property, by cancer cells. We discovered ADAM 17 degrades interferon gamma for the first time.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] Nrf2 Activation Attenuates Both Orthodontic Tooth2015
Author(s)
Kanzaki, H., Shinohara, F., Kajiya, M., Fukaya, S., Miyamoto, Y., & Nakamura, Y.
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Journal Title
Journal of Dental Research.
Volume: in press
Related Report
Peer Reviewed / Acknowledgement Compliant
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