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作 者:邓云秋 DENG Yunqiu(Department of Neurosurgery,Tianjin Jinghai District Hospital 30160)
出 处:《医学理论与实践》2018年第9期1260-1261,1270,共3页The Journal of Medical Theory and Practice
摘 要:目的:探析异甘草素对脑胶质瘤U251细胞增殖、凋亡的影响,并总结其相关机制。方法:采用浓度不等的异甘草素处理脑胶质瘤U251细胞样本,同时对10、20、40、60、80μmol/L各浓度设5个复孔,均处理24h、48h、72h;采取流式细胞术对细胞凋亡变化检测,由四甲基偶氮唑蓝(MTT)对细胞增殖能力检测,核糖体RNA(mRNA)、叉头框蛋白M1(FoxM1)表达水平则采取逆转录-聚合酶链反应(RT-PCR)法检测。结果:脑胶质瘤U251细胞经浓度不同的异甘草素处理后,细胞增殖均受到程度不一的抑制表现,在同作用时间,但不同浓度之间差异具有统计学意义(P<0.05);反之,在相同浓度,但作用时间不同细胞增殖情况的差异同样具有统计学意义(P<0.05);在对细胞凋亡影响方面,随着异甘草素浓度不同作用细胞24h后,细胞凋亡率随着异甘草素浓度增加出现正比增加趋势(P<0.05);在FoxM1、mRNA相对表达水平中,不同浓度间异甘草素处理细胞48h后差异具有统计学意义(P<0.05)。结论:异甘草素可理想抑制脑胶质瘤U251细胞增殖,并有效诱导其凋亡作用机制,这可能与下FoxM1基因表达水平正相关。Objective:To investigate the effect of iso glycyrrhizin on the proliferation and apoptosis of glioma U251 cells,and to summarize the related mechanisms.Methods:Using different concentrations of glycyrrhizin treatment samples of glioma U251 cells,and in 10,20,40,60,80 different concentration ofμmol/L with 5 holes,24 h,48 h,72 hwere taken on the change of apoptosis;flow cytometry,four by methyl thiazolyl tetrazolium(MTT)on cell proliferation detection,ribosomal RNA(mRNA),forkhead box protein M1(FoxM1)expression by reverse transcriptase polymerase chain reaction(RT-PCR)assay.Results:Glioma U251 cell proliferation was inhibited the level of performance,at the same time,but the difference between different concentrations were statistically significant(P〈0.05);on the other hand,in the same concentration,but the effect of different time of cell proliferation was also statistically significant(P〈0.05);the effect on cell apoptosis,with different concentration of isoliquiritigenin cells after 24 h,apoptosis rate with isoliquiritin concentration increased proportional increase(P〈0.05);the level of FoxM1 and mRNA expression in different concentration of isoliquiritigenin treated cells 48 hwas statistically significant difference(P〈0.05).Conclusion:Iso glycyrrhizin has an inhibitory effect on the proliferation and apoptosis of glioma U251 cells,which may be positively correlated with the expression level of FoxM1 gene.
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