Galectin-1-expression and effect on proliferation and migration of glioma cells
Herwig Strik, Katy Schmidt, Paul Lingor, Lars Tönges, Jörg Wischhusen, Michael Weller, Mathias Bähr
Abstract
Herwig Strik, Katy Schmidt, Paul Lingor, Lars Tönges, Jörg Wischhusen, Michael Weller, Mathias Bähr
Abstract
Galectins are evolutionarily highly conserved, glycoprotein- recognizing lectins involved in numerous physiological and pathological processes. Galectin-1 (Gal-1) has been associated with migration and invasion in malignant gliomas. We examined here the expression of Gal-1 in glioma cell lines and its influence on proliferation and migration. We detected Gal-1 in all 12 tested cell lines by Western Blot and flow cytometry. Levels of Gal-1 were higher in the tumour cells than in normal brain and higher in cell lines with wildtype as compared with mutated p53. Irradiation induced Gal-1 expression. Recombinant Gal-1 moderately enhanced proliferation in U118 cells and migration in A172 and U118 glioma cells. Downregulation with RNA-interference resulted in reduced proliferation in A172 cells and migratory capacity in both tested glioma cell lines. Our data confirm previous data on the impact of Gal-1 on the migration of glioma cells. Therefore, Gal-1 may be an interesting target to modulate migration and invasion in human gliomas.
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Galectins are evolutionarily highly conserved, glycoprotein- recognizing lectins involved in numerous physiological and pathological processes. Galectin-1 (Gal-1) has been associated with migration and invasion in malignant gliomas. We examined here the expression of Gal-1 in glioma cell lines and its influence on proliferation and migration. We detected Gal-1 in all 12 tested cell lines by Western Blot and flow cytometry. Levels of Gal-1 were higher in the tumour cells than in normal brain and higher in cell lines with wildtype as compared with mutated p53. Irradiation induced Gal-1 expression. Recombinant Gal-1 moderately enhanced proliferation in U118 cells and migration in A172 and U118 glioma cells. Downregulation with RNA-interference resulted in reduced proliferation in A172 cells and migratory capacity in both tested glioma cell lines. Our data confirm previous data on the impact of Gal-1 on the migration of glioma cells. Therefore, Gal-1 may be an interesting target to modulate migration and invasion in human gliomas.
Key concepts: Galectin, Galectin-1, Glioma, Galectin-3, Cell biology, Biology, Glycoprotein, Cancer research