2010 Fiscal Year Final Research Report
Analysis of common molecular mechanisms and pharmaceutical research in cancer invasion and angiogenesis
Project/Area Number |
20590293
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General medical chemistry
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Research Institution | Osaka Bioscience Institute |
Principal Investigator |
HASHIMOTO Ari Osaka Bioscience Institute, 大学院・医学研究科, 助教 (60390803)
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Research Collaborator |
京都大学, 医学部
オックスフォード大学, Weatherall Institute of Molecular Medicine Cell Signalling
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Project Period (FY) |
2008 – 2010
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Keywords | 血管新生 / 癌浸潤 / Arf6 / AMAP1 / ArfGEF / 乳癌 / チロシンリン酸化 |
Research Abstract |
We have shown that GEP100 links EGFR signaling to Arf6 activation to induce invasive activities of some breast cancer cells. Our analyses demonstrate that the same GEP100-Arf6-AMAP1 pathway is essential for VEGF-induced angiogenesis activities, and that VEGFR2, via phospho-Tyr951, binds to the PH domain of GEP100 to activate the Arf6-AMAP1 pathway to induce angiogenesis. Moreover, we found the small compound that inhibits the interaction between GEP100 and VEGFR-2. The GEP100-Arf6-AMAP1 pathway, activated by receptor tyrosine kinases, appears to be common in angiogenesis and cancer invasion, and provide their new therapeutic targets from a pathological analysis.
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[Journal Article] The EGFR-GEP100-Arf6-AMAP1 signaling pathway specific to breast cancer invasion and metastasis.2009
Author(s)
Sabe, H., Hashimoto, S., Morishige, M., Hashimoto, A., Ogawa, E., Nam, J.M, Miura, K., Yano, H., Onodera, Y.
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Journal Title
Traffic 10
Pages: 982-993
Peer Reviewed
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[Journal Article] GEP100 links EGFR signaling to Arf6 activation to induce breast cancer invasion.2008
Author(s)
Morishige , M., Hashimoto, S., Ogawa, E., Toda, Y., Kotani, H., Hirose, M., Wei, S., Hashimoto, A., Yamada, A., Yano, H., Mazaki, Y., Kodama, H., Nio, Y., Manabe, Y., Wada, H., Kobayashi, H., ^*Sabe, H.
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Journal Title
Nat Cell Biol. 10
Pages: 85-92
Peer Reviewed
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[Remarks] ホームページ等