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作 者:何东杰[1,2] 胡静[1] 梁军[2] 张洁琼[3] 康蓓佩 骆文静[3] 石梅[1] 魏丽春[1]
机构地区:[1]第四军医大学西京医院放射治疗科,西安710032 [2]第四军医大学唐都医院放射治疗科,西安710038 [3]第四军医大学劳动与环境卫生教研室,西安710032
出 处:《神经解剖学杂志》2015年第3期303-308,共6页Chinese Journal of Neuroanatomy
基 金:国家自然科学基金(81272346;81201749)
摘 要:目的:探讨Wnt信号通路在胶质瘤细胞增殖和生长迁移中的可能作用。方法:建立U251胶质瘤细胞培养体系、并给予不同浓度Wnt信号通路的抑制剂(IWR-1 0,2.5,5.0,10μmol/L)处理后,MTT测定增殖活力、划痕实验测定生长迁移、Western Blot测定Wnt5a、β-catenin蛋白表达水平,分析IWR-1的生物作用与效应途径。结果:MTT表明胶质瘤细胞的IWR-1 5.0、10μmol/L处理24 h、48 h组,细胞增殖活力显著低于对照组(P〈0.05~0.01)。划痕检测表明IWR-1 5.0、10μmol/L处理48 h组胶质瘤细胞的生长迁移能力低于对照组(P〈0.05~0.01)。Western Blot表明IWR-1处理48 h组胶质瘤细胞的β-catenin蛋白表达水平低于对照组(P〈0.05~0.01)。结论:Wnt信号抑制剂IWR-1能够明显抑制人胶质瘤细胞增殖和生长迁移,提示Wnt/β-catenin信号途径可能具有胶质瘤干预治疗靶点的潜在价值。Objective: To investigate possible involvement of Wnt signaling pathway in cell proliferation and migration of glioma cell. Methods: Cell culture of U251 glioma cell line was established and treated by different concentrations of Wnt signing inhibitor( inhibitors of Wnt response-1,IWR-1,0,2. 5,5. 0,10 μmol / L). Cell proliferation was measured by MTT. Cell migration was detected by wound healing. The expression of Wnt5 a and β-catenin proteins was detected by Western Blot. Results: Cell proliferation in U251 glioma cells treated by 5. 0 and 10 μmol / L IWR-1 was lower than that in the control group( P〈0. 05,P〈0. 01). The ability of migration in glioma cells treated by 5. 0 and 10 μmol / L IWR-1 was weaker than that of control group at 48 h( P〈0. 05,P〈0. 01). The expression of β-catenin protein in glioma cells treated by 5. 0 and 10 μmol / L IWR-1 was lower than that of control group at 48 h( P〈0. 05,P〈0. 01). Conclusion: IWR-1 might significantly inhibit cell proliferation,growth and migration of U251 glioma cells,suggesting that Wnt /β-catenin signaling pathway may be a potential intervention target for therapeutic treatment of glioma.
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