2017 Fiscal Year Final Research Report
A new strategy for treatment of HCC by regulating hepatic stellate cell
Project/Area Number |
15K10165
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Digestive surgery
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Research Institution | Department of Clinical Research, National Hospital Organization Kure Medical Center |
Principal Investigator |
Tashiro Hirotaka 独立行政法人国立病院機構(呉医療センター臨床研究部), その他部局等, その他 (90359894)
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Project Period (FY) |
2015-04-01 – 2018-03-31
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Keywords | 肝細胞癌 / 肝星細胞 / 癌間質 / アンチトロンビン |
Outline of Final Research Achievements |
Antithrombin (AT) is not only a major regulator of hemostasis, but also has anti-inflammatory properties. We aimed to investigate whether AT is associated with development of HCC. Liver tumors were developed in ATIII-insufficient (AT+/-) mice and wild-type (AT+/+) mice treated with DEN and CCl4. Tumor size and the number of DEN and CCl4-induced liver tumors were significantly enhanced in AT-insufficient mice compared with wild-type mice. The serum transaminases, cell death and expression of cleaved caspase-3 in livers were exaggerated in AT-insufficient mice compared with wild-type mice. The level of 8-OHdG, a marker of oxidative DNA damage, in liver was significantly increased in AT-insufficient mice compared with wild-type mice. AT insufficiency led to the increased susceptibility to liver-tumorigenesis through amplifying inflammation.
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Free Research Field |
消化器外科
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