The development of a novel type of cancer preventive medicine that targets cell competition
Project/Area Number |
25830109
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Tumor therapeutics
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Research Institution | University of Yamanashi (2014-2015) Hokkaido University (2013) |
Principal Investigator |
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
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Keywords | 癌 / 細胞・組織 / 細胞競合 / ケミカルバイオロジー / 抗がん物質探索 / 組織 |
Outline of Final Research Achievements |
Our recent studies have revealed that cell competition can occur between normal and transformed epithelial cells, and normal epithelial cells recognize the presence of the neighboring transformed cells and actively eliminate them cells from epithelial tissues. We forcused this interaction and established the screening platform that targets cell competition. By using this platform, we have identified VC1 as a hit compound that specifically promotes elimination of RasV12-transformed cells from the epithelium. Among several VC1 derivative compounds, we have found that VC1-8 has least cytotoxicity against normal cells but shows the comparable effect on the elimination of transformed cells. This cell competition activity of VC1-8 is observed both in vitro and ex vivo, indicating that VC1-8 is a promising novel type of cancer preventive medicine.
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Report
(4 results)
Research Products
(6 results)
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[Journal Article] The cell competition-based high-throughput screening identifies small compounds that promote the elimination of RasV12-transformed cells from epithelia.2015
Author(s)
Yamauchi, H., Matsumaru, T., Morita, T., Ishikawa, S., Maenaka, K., Takigawa, I., Semba, K., Kon, S. and Fujita, Y.
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Journal Title
Scientific Reports
Volume: 5
Issue: 1
Pages: 15336-15336
DOI
NAID
Related Report
Peer Reviewed / Open Access
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