Expression analysis and treatment possibility of intr-aocular anti-angiogenic factor
| Project/Area Number |
16591751
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Ophthalmology
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| Research Institution | Osaka University |
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Principal Investigator |
OSHIMA Yusuke Osaka University, Graduate School of Medicine, Assistant, 医学系研究科, 助手 (20362717)
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| Co-Investigator(Kenkyū-buntansha) |
KAMEI Motohiro Osaka University, Graduate School of Medicine, Associate Professor, 医学系研究科, 助教授 (40281125)
IKUNO Yasushi Osaka University, Graduate School of Medicine, Assistant, 医学系研究科, 助手 (50294096)
TANO Yasuo Osaka University, Graduate School of Medicine, Professor, 医学系研究科, 教授 (80093433)
OHJI Masahito Shiga University of Medical Science, Faculty of Medicine, Professor, 医学部, 教授 (90252650)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2005: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2004: ¥2,100,000 (Direct Cost: ¥2,100,000)
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| Keywords | anti-angiogenesis / vascular endothelial cell / Chondromodulin / Tenomodulin / gene expression / VEGF / anti-tumor therapy / 細胞増殖 / 細胞接着 / 管腔形成 |
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| Research Abstract |
Using a adenovirus expression system, we utilized the forced expression and subsequent secretion of the Chondromodulin-I (ChM-I) and Tenomodulin (TeM) C-terminal domains in human retial vascular endothelial cells (VECs) and retinal pigment epithelial cells to show the anti-angiogenic function of the C-terminal domains. Both human ChM-I and TeM C-terminal domains significantly suppressed the cell adhesion, migration, cell growth and tube forming activity of two kinds of VECs. The suppression activity was prominent on vitronectin-coated dishes indicating the suppression mechanism closely related to the integrin families (αvβ3,αvβ5). Furthermore, the transduction of either TeM or ChM-I C-terminal domain in melanoma cells resulted in suppression of tumor growth in associated with decreased vessels density in vivo. Here, we have showed that both TeM and ChM-I C-terminal domains exhibit anti-angiogenic and anti-tumor activities when expressed in a secreted form.
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Report
(3 results)
Research Products
(29 results)
