New stomach cancer model mouse using Cre expression H. pylori
Project/Area Number |
15K19315
|
Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Gastroenterology
|
Research Institution | The Institute for Adult Diseases Asahi Life Foundation |
Principal Investigator |
Nobumi Suzuki 公益財団法人朝日生命成人病研究所, その他部局等, 教授(移行) (30723746)
|
Project Period (FY) |
2015-04-01 – 2017-03-31
|
Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2016: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2015: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
|
Keywords | ピロリ菌 / 胃癌 |
Outline of Final Research Achievements |
It is a well-known that H. pylori infection causes stomach cancer. On the other hand, H. pylori that can not infect C57BL / 6 mice, which is the source of genetically modified mice. This was a obstacle in mouse experiments. Recently it has been reported that PMSS 1 strain can infect. We confirmed that the PMSS 1 strain can infect B6 mice. Then we made the gastritis mice model by useing PMSS1 strain and we reported a paper that IL - 1 signal and SOX 9 are involved in intestinal metaplasia. Subsequently, PMSS 1 strain did not express Cre, but we make CagA of PMSS1 to be KO and we confirmed activation of stress MAPK was dependent on CagA.
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Report
(3 results)
Research Products
(1 results)
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[Journal Article] Gastric Metaplasia Induced by Helicobacter pylori Is Associated with Enhanced SOX9 Expression via Interleukin-1 Signaling.2015
Author(s)
Serizawa T, Hirata Y, Hayakawa Y, Suzuki N, Sakitani K, Hikiba Y, Ihara S, Kinoshita H, Nakagawa H, Tateishi K, Koike K.
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Journal Title
Infection and Immunity
Volume: 84
Issue: 2
Pages: 562-572
DOI
Related Report
Peer Reviewed