Inhibition of FGF receptor activity in glioma implanted into the mouse brain using the tetracyclin-regulated expression system
Autor: | Paul Canioni, Raphael Pineau, Eric Thiaudière, Sylvie Lemière, J.-M. Franconi, Patrick Auguste, Andreas Bikfalvi, Lorenzo Bello, M. Pluderi, Sylvain Miraux |
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Rok vydání: | 2004 |
Předmět: |
Vascular Endothelial Growth Factor A
Cancer Research Physiology Angiogenesis Genetic Vectors Clinical Biochemistry Apoptosis Biology Transfection Fibroblast growth factor Neovascularization Mice Cell Line Tumor Glioma medicine Animals Receptor Fibroblast Growth Factor Type 2 Receptor Cell Proliferation Neovascularization Pathologic Cell growth Brain Receptor Protein-Tyrosine Kinases Tetracycline medicine.disease Receptors Fibroblast Growth Factor Rats Gene Expression Regulation Cell culture Immunology Cancer research medicine.symptom Neoplasm Transplantation |
Zdroj: | Angiogenesis. 7:105-113 |
ISSN: | 1573-7209 0969-6970 |
DOI: | 10.1007/s10456-004-1037-0 |
Popis: | We have investigated growth and vascularization of malignant glioma in mice upon conditional inhibition of fibroblast growth factor (FGF) receptor activity. C6 rat glioma cells were transfected with a dominant-negative fibroblast growth factor receptor-2 (FGFR2-DN) cDNA under the control of a tetracycline-regulated expression promoter (tet off) and implanted in the brain of immunodeficient mice. Magnetic resonance imaging analysis showed a significant decrease in tumor growth 14 days after implantation when FGFR2-DN was expressed compared to control. This size difference disappeared after 20 days. However, after 20 days, tumor and endothelial cells apoptosis were higher in the FGFR2-DN group and consequently angiogenesis was decreased whereas tumor cells were similarly associated with blood vessels at the tumor periphery. Pericyte coverage was not different between the two groups but a higher amount of pericytes not associated with vessels was found in the FGFR2-DN expressing group. This demonstrates, that conditional expression of inhibitor of FGF receptor activity in gliomas implanted in the brain of immunodeficient mice can be achieved efficiently, and that FGFs are major players in glioma development and in glioma angiogenesis. |
Databáze: | OpenAIRE |
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