| Project/Area Number |
15K08304
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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 |
Pathological medical chemistry
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| Research Institution | Tottori University |
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Principal Investigator |
KUGOH Hiroyuki 鳥取大学, 医学(系)研究科(研究院), 教授 (40225131)
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| Co-Investigator(Renkei-kenkyūsha) |
OHBAYASHI Tetsuya 鳥取大学, 生命機能研究支援センター, 准教授 (80348804)
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| Research Collaborator |
OHIRA Takahito
INAOKA Daigo
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| Project Period (FY) |
2015-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2017: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | がん / SASP / 細胞老化 / 個体老化 / 炎症 / PITX1 / テロメレース / OIS / テロメア / ＰＩＴＸ１ / がん抑制遺伝子 / IL-6 / 炎症反応 / TERT / IL-8 |
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| Outline of Final Research Achievements |
In this study, we investigated the role of PITX1 in the SASP pathway and conducted research to clarify the relationship between cellular senescence and carcinogenesis mechanism. As a result, we found that PITX1 is directly involved in the positive expression regulation of both IL-6 and IL-8, which are known as the major marker factors of the SASP pathway. Furthermore, it was accompanied by increased p16 mRNA transcription level which known cell senescence factor in the SASP pathway. On the other hand, we succeeded in establishing of the Pitx1 KO mouse which can conditionally knock down of Pitx1 gene allele. These results suggested that PITX1 may function as a novel regulatory factor in a series of molecular signals in the SASP pathway.
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