C6 cell line and human glioblastoma cells contained 1% cells which were ABCG2 positive.
C6细胞系和人胶质母细胞瘤细胞中均发现有1%左右的细胞ABCG2蛋白表达阳性。
Objective To investigate the effects of matrine on the proliferation of brain glioma C6 cell line in vitro.
目的观察苦参碱对脑胶质瘤C6细胞株体外增殖的影响。
Conclusions SPB can apparently inhibit the proliferation of C6 cells and can induce cell differentiation and even apoptosis of C6 cells.
结论苯丁酸钠可明显抑制C6细胞增殖，诱导细胞分化，甚至诱发细胞凋亡。
Objective To establish brain glioma models in rats with different-volume C6 cell suspension by stereotaxic implantation and to compare the growth patterns of the intracranial tumors.
目的用不同接种体积立体定向建立大鼠C6脑胶质瘤模型，比较其生长特性。
Results The C6 glioma cell apoptosis induction of GFP contained serum in vitro could be confirmed by morphological examination, flow cytometry analysis and TUNEL method.
结果形态学变化、流式细胞仪分析和TUNEL法结果均证实含鲜壁虎血清在体外可诱导C6胶质瘤细胞凋亡；
Objective to observe the affect of vascular endothelial growth factor (VEGF) antibody on the cell apoptosis and growth of rat C6 glioma.
目的观察血管内皮生长因子(VEGF)抗体对大鼠c6胶质瘤细胞凋亡的影响及对肿瘤生长的抑制作用。
Conclusion: Matrine can induce C6 glioma cell apoptosis and the mechanism might be related to a number of genes involved in death receptor pathway and mitochondrial pathway.
结论：苦参碱能诱导C6胶质瘤细胞的凋亡，其机制与死亡受体途径和线粒体途径的众多基因有关。
To explore the effects of IL-18 gene transfection on the proliferation of C6 glioma cell.
探讨IL-18基因转染对大鼠C6胶质瘤细胞生长特性的影响。
Methods: After establishing a C6/SD glioma model, by using flow cytometric analysis, immunohistochemistry and HE stain three methods, the proliferation kinetics in C6 glioma cell was measured.
方法：建立C6/SD大鼠胶质瘤模型后，应用流式细胞仪检测、免疫组化、HE染色三种方法，研究C6胶质瘤细胞的增殖动力学指标。
AIM: to investigate the effects of exogenous cell-permeable C2-ceramide on viability and early apoptosis induction in rat glioma ce ll C6.
目的：研究外源性C2神经酰胺对大鼠脑胶质瘤细胞C6活力的抑制作用以及早期凋亡诱导作用。
Methods The growth rate and recovery of C6/36 cell was evaluated. MTT, inverted microscope observation was using in this study to observe the effects of piperine on cell multiplication.
方法采用冲击测试法测定胡椒碱对白纹伊蚊C6/36细胞株生长率及核分裂的影响，相差显微镜对细胞进行形态学观察，并观察受损细胞的恢复；
Methods: Plate clonality assays was used to measure the impact of cell density to cell clonality and cell cycle in BT325,786-0,293, C6 and NIH3T3 cell lines.
方法：利用平板克隆形成实验检测五种细胞系bt325、786- 0、293、C6和NIH3T3的克隆形成能力，分析细胞密度或细胞数量对这些细胞系的克隆形成能力及细胞周期的影响。
This study was designed to investigate the effects of exogenousRGS16 gene transfection on the growth of rat glioma cell line C6.
本研究旨在探讨RGS16基因转染对大鼠胶质瘤C6细胞生长的影响。
Cell inhibition rate (IR) was calculated after C6 glioma cells were cultured in the controlled drug release system for testifying tumor-killing effect of the controlled drug release system.
利用C6胶质瘤细胞在药物缓释体中培养后计算细胞抑制率(IR)验证药物缓释体的缓释杀瘤效果。
Conclusion the Pingliukang medicated serum can inhibit the proliferation and block cell cycle of cultured C6 glioma cells.
结论平瘤康含药血清可能通过阻滞细胞周期而抑制胶质瘤细胞增殖。
Conclusion BCNU loaded PLGA wafer can inhibit the proliferation of C6 glioma cell and demonstrate gradually increased tendency with prolonged release time.
结论BCNU PLGA缓释微球可以抑制C6胶质瘤细胞的增殖，随释放时间延长细胞生长抑制率逐渐上升。
Conclusion BCNU loaded PLGA wafer can inhibit the proliferation of C6 glioma cell and demonstrate gradually increased tendency with prolonged release time.
结论BCNU PLGA缓释微球可以抑制C6胶质瘤细胞的增殖，随释放时间延长细胞生长抑制率逐渐上升。
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