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KIF20A对胶质瘤细胞增殖、迁移和侵袭、凋亡及细胞周期分布的影响
引用本文:刘纪营,吴妍妍,赵 杰,张五松,靳振伟,陈健辉,郭新宾.KIF20A对胶质瘤细胞增殖、迁移和侵袭、凋亡及细胞周期分布的影响[J].现代肿瘤医学,2020,0(17):2943-2947.
作者姓名:刘纪营  吴妍妍  赵 杰  张五松  靳振伟  陈健辉  郭新宾
作者单位:1.项城市中医院介入科;2.脑病科;3.神经内科,河南 项城 466200;4.郑州大学第一附属医院神经介入科,河南 郑州 450000
基金项目:河南省高等学校重点科研项目(编号:19A320034)
摘    要:目的:研究KIF20A对胶质瘤U87细胞系增殖、侵袭、迁移、凋亡及细胞周期分布的影响。方法:利用 RNA干扰技术下调胶质瘤细胞系 U87中 KIF20A 的表达。RT-qPCR 和 Western blot 分别检测 KIF20A 在mRNA 和蛋白水平上的表达。CCK-8 实验检测 U87细胞增殖能力的变化,Transwell 实验检测U87细胞迁移及侵袭能力的变化,流式细胞术检测 U87细胞凋亡及细胞周期的变化。结果:RT-qPCR和Western blot 结果显示 siRNA-KIF20A显著下调 KIF20A 的表达,CCK-8和Transwell 实验显示下调 KIF20A 的表达显著抑制了U87细胞的增殖、迁移及侵袭能力,流式细胞术结果显示下调 KIF20A 的表达显著促进了U87细胞的凋亡,诱导细胞周期阻滞在G0/G1期。结论:下调KIF20A的表达抑制胶质母细胞瘤细胞的增殖、迁移及侵袭,促进胶质母细胞瘤细胞的凋亡并诱导细胞周期G0/G1期阻滞。

关 键 词:胶质瘤  KIF20A  siRNA  生物学功能

Effects of KIF20A on the proliferation,migration and invasion,apoptosis and cell cycle distribution of glioma cells
Liu Jiying,Wu Yanyan,Zhao Jie,Zhang Wusong,Jin Zhenwei,Chen Jianhui,Guo Xinbin.Effects of KIF20A on the proliferation,migration and invasion,apoptosis and cell cycle distribution of glioma cells[J].Journal of Modern Oncology,2020,0(17):2943-2947.
Authors:Liu Jiying  Wu Yanyan  Zhao Jie  Zhang Wusong  Jin Zhenwei  Chen Jianhui  Guo Xinbin
Affiliation:1.Intervention Section;2.Department of Encephalopathy;3.Department of Neurology,Xiangcheng Traditional Chinese Medicine Hospital,Henan Xiangcheng 466200,China;4.Department of Neurointervention,the First Affiliated Hospital of Zhengzhou University,Henan Zhengzhou 450000,China.
Abstract:Objective:To study the effect of KIF20A on proliferation,invasion,migration,apoptosis and cell cycle distribution of human glioma cell line U87.Methods:RNA interference technique was used to down-regulate the expression of KIF20A in glioma cell line U87.RT-qPCR and Western blot were used to detect the expression of KIF20A at mRNA and protein levels,respectively.The change of proliferation ability of U87 cells was detected by CCK-8 experiment.The change of migration and invasion ability of U87 cells was detected by Transwell experiment,and the change of apoptosis and cell cycle of U87 cells was detected by flow cytometry.Results:The results of RT-qPCR and Western blot showed that siRNA-KIF20A significantly reduced the expression of KIF20A.The CCK-8 and Transwell experiments showed that down-regulation of KIF20A expression significantly inhibited the proliferation,migration and invasion of U87 cells.Flow cytometry showed that down-regulation of KIF20A expression significantly promoted apoptosis of U87 cells and induced cell cycle arrest in G0/G1 phase.Conclusion:Down-regulation of KIF20A expression inhibits proliferation,migration and invasion of glioblastoma cells,promotes apoptosis of glioblastoma cells and induces cell cycle G0/G1 phase arrest.
Keywords:glioma  KIF20A  siRNA  biological function
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