2015 Fiscal Year Final Research Report
Investigation of cancer therapeutic method without side effects: Suppression mechanisms of cancer metastasis on the lung by CXCL14/BRAK
Project/Area Number |
25293384
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Partial Multi-year Fund |
Section | 一般 |
Research Field |
Pathobiological dentistry/Dental radiology
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Research Institution | Kanagawa Dental College |
Principal Investigator |
Hata Ryu-Ichiro 神奈川歯科大学, 歯学研究科(研究院), その他 (10014276)
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Co-Investigator(Kenkyū-buntansha) |
MAEHATA YOJIROU 神奈川歯科大学, 大学院歯学研究科, 講師 (80410009)
IZUKURI KAZUHITO 神奈川歯科大学, 大学院歯学研究科, 講師 (90257296)
AKASAKA TETSU 神奈川歯科大学, 大学院歯学研究科, 助教 (60316263)
MIYAMOTO CHIHIRO 神奈川歯科大学, 大学院歯学研究科, 特別研究員 (50633963)
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Co-Investigator(Renkei-kenkyūsha) |
TAKEDA KAZUYOSHI 順天堂大学, 大学院医学研究科, 准教授 (80272821)
MUKAIDA NAOFUMI 金沢大学, がん伸展制御研究所, 教授 (30182067)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Keywords | 癌抑制分子 / ケモカイン / 転移抑制 / 副作用のない癌抑制法 / 余命の延長 |
Outline of Final Research Achievements |
The main cause of Japanese death is due to the recurrence of cancer, and metastasis. We have previously reported that the rate of carcinogenesis, the growth of tumor transplants and metastasis in CXCL14 over-expressed transgenic (Tg) mouse were significantly lower compared with that for isogenic wild type C57BL/6 (Wt) mice. Here we investigated suppression mechanisms of metastasis by CXCL14 using the pulmonary metastasis system of the malignant melanoma cell and the cell culture system. It was found that CXCL14 and interferon-γ (IFN-γ) secreted by the activated natural killer (NK)T cells, and also IFN-γ secreted by activated natural killer cells synergistically suppressed the metastasis of the cells on the lungs.
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Free Research Field |
腫瘍抑制機構
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