2013 Fiscal Year Final Research Report
Novel angiogenesis inhibitor DBP-maf for cancer therapy
Project/Area Number |
23659611
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
General surgery
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Research Institution | Osaka University |
Principal Investigator |
MATSUURA Nariaki 大阪大学, 医学(系)研究科(研究院), 教授 (70190402)
|
Co-Investigator(Kenkyū-buntansha) |
MORI Seiji 大阪大学, 大学院医学系研究科, 助教 (90467506)
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Co-Investigator(Renkei-kenkyūsha) |
HAMADA Yoshinosuke 大阪大学, 大学院医学系研究科, 特任助教 (10362683)
|
Project Period (FY) |
2011 – 2013
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Keywords | 血管新生 / マクロファージ / がん治療 |
Research Abstract |
DBP-maf (Vitamin D binding protein-macrophage activating factor) showed inhibitory activity for angiogenesis through suppressive effect on endothelial proliferation, adhesion activity to extracellular matrix proteins, migration capacity, and tube formation. DBP-maf inhibits markedly angiogenesis by Aorta ring assay, Das assay and Matrigel plague assay. Furthermore DBP-maf has stimulatory effect on macrophage activation. DBP-maf suppresses growth of hepatocellular carcinoma or pancreatic carcinoma cell lines in vivo.
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[Journal Article] A Dominant-Negative FGF1 Mutant (the R50E Mutant) Suppresses Tumorigenesis and Angiogenesis2013
Author(s)
Mori S, Tran V, Nishikawa K, Kaneda T, Hamada Y, Kawaguchi N, Fujita M, Takada YK, Matsuura N, Zhao M, Takada Y
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Journal Title
PLoS One
Volume: 8(2) (Epub)
Pages: e57927
DOI
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