| Project/Area Number |
23591894
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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 |
General surgery
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| Research Institution | Kyushu University |
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Principal Investigator |
ONISHI Hideya 九州大学, 医学(系)研究科(研究院), 准教授 (30553276)
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| Co-Investigator(Kenkyū-buntansha) |
KATANO Mitsuo 九州大学, 大学院医学研究院, 教授 (10145203)
NAKANO Kenji 九州大学, 先端融合医療レドックスナビ 研究拠点, 教授 (00315061)
NAKAMURA Katsuya 九州大学, 大学病院, 助教 (60585743)
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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 |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
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| Keywords | 制御性T細胞 / VEGFR2 / FOXP3 / 細胞障害性T細胞 / 抗腫瘍効果 / 制御性Ｔ細胞 / 細胞障害性Ｔ細胞 / 大腸がん / 予後予測因子 / VEGF |
|---|
| Research Abstract |
Relation between the number of tumor-infiltrated VEGFR2+ regulatory T (Treg) cells and prognosis in colorectal cancer patients with curative surgical resection was analyzed. The number of tumor-infiltrated VEGFR2+FOXP3+Treg cells was an independent prognostic factor for colorectal cancer. These results indicate the validity that VEGFR2+ Treg could be a therapeutic target. In vitro experiment, protein-bound polysaccharide, basiliximab, Cox-2 inhibitor and bevacizumab significantly reduced Treg number. Activate T lymphocytes induced after the depletion of Treg using basiliximab showed the increase of cytotoxicity against cancer cells.
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