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Effects of CENP-W down-regulation on human glioma U87 cells
Authors:JI Qian-kun  LI Jian-bin  FAN Yang-hua  XU Bin  CHAI Yi  JI Chen-xing  ZHU Xin-gen
Institution:1. Department of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical College, Xinxiang 453100, China; 2. Department of Neurosurgery, The Second Hospital of Nanchang City, Nanchang 330006, China; 3. Department of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China
Abstract:AIM: To study the effect of centromere protein W (CENP-W) down-regulation on human glioma U87 cells.METHODS: Small interfering RNA (siRNA) was used to inhibit the expression of CENP-W in the U87 cells. The interference effect of siRNA was evaluated by RT-qPCR and Western blot. The proliferation of the cells was analyzed by MTT assay, BrdU staining and colony formation experiment. Transwell chamber assay was used to detect the invasion ability of the cells. The cell migration ability was measured by a scratch test. The changes of the cell cycle distribution and apoptosis were analyzed by flow cytometry.RESULTS: The results of MTT assay, colony formation experiment and BrdU staining showed that the cell proliferation and colony formation abilities in experimental group were significantly lower than those in control group and negative control group. The results of Transwell and scratch experiments showed that the migration and invasion abilities in experimental group were weaker than those in blank control group and negative control group. The results of flow cytometry analysis showed that the cell cycle distribution in experimental group was arrested in G0/G1 phase. The percentage of apoptotic cells in experimental group was higher than that in control group (P<0.05).CONCLUSION: Down-regulation of CENP-W expression inhibits the proliferation, migration and invasion of human glioma cells and promotes the apoptosis of the cells, suggesting that CENP-W may be a potential target of gene therapy for human glioma.
Keywords:Centromere protein W  Small interfering RNA  Cell proliferation  Cell invasion  
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