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Glycogen synthase kinase-3β regulates astrocytic differentiation of U87-MG human glioblastoma cells

  
@article{APS6644,
	author = {Yan Li and Hui-min Lu and Gang Li and Guang-mei Yan},
	title = {Glycogen synthase kinase-3β regulates astrocytic differentiation of U87-MG human glioblastoma cells},
	journal = {Acta Pharmacologica Sinica},
	volume = {31},
	number = {3},
	year = {2016},
	keywords = {},
	abstract = {Aim: To evaluate the role of glycogen synthase kinase-3β (GSK-3β) in the induced differentiation of human glioblastoma cells.
Methods: Cell proliferation was determined by bromodeoxyuridine (BrdU) incorporation assay. The protein level of p-GSK-3β, GSK-3β, glial fibrillary acidic protein (GFAP) and proliferating cell nuclear antigen (PCNA) were determined using Western blots. The overexpression of mutant GSK-3β was analyzed by immunocytochemistry.
Results: The biotoxin cholera toxin is capable of inducing differentiation of U87-MG human glioblastoma cells, which is characterized by morphological changes to astrocytic phenotype, increase in differentiation marker protein GFAP and decrease in proliferation. GSK-3β activation is induced during this differentiation. Small interfering RNA against GSK-3β suppresses the induced-differentiation in U87-MG cells. Conversely, overexpression of a constitutively active form of human GSK-3β (pcDNA3-GSK-3β-S9A) mutant leads to differentiation of U87-MG cells.
Conclusion: Our findings suggest that GSK-3β plays an important role in astrocytic differentiation of human glioblastoma cells and may be a novel therapeutic target in the malignant tumor.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/6644}
}