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作 者:任凌燕[1] 徐磊[1] 赵青[1] 罗皓[1] 赵怡[1]
机构地区:[1]解放军第四五四医院,210000
出 处:《实用癌症杂志》2016年第2期202-204,209,共4页The Practical Journal of Cancer
摘 要:目的研究β-榄香烯对人食管癌细胞EC9706增殖、凋亡及caspase-3表达的影响。方法采用不同浓度的β-榄香烯(0、10、20、30、40、50μg/ml)处理细胞24 h,CCK-8测定细胞增殖活力。以50μg/mlβ-榄香烯处理细胞0、6、12、24 h,CCK-8测定细胞增殖活力。以不加β-榄香烯组作为对照组,选取50μg/mlβ-榄香烯处理细胞24 h,流式细胞术测定细胞凋亡率,分光光度法测定caspase-3活性。结果随着β-榄香烯浓度的增加,人食管癌细胞增殖活力逐渐下降,呈浓度依赖性(P<0.05)。以50μg/mlβ-榄香烯处理细胞0、6、12、24 h,随着时间的增加,细胞增殖活力下降,呈现时间依赖性(P<0.05)。相比对照组,50μg/mlβ-榄香烯处理细胞24 h后细胞凋亡明显增加(P<0.05),caspase-3活性明显增加(P<0.05)。结论β-榄香烯可抑制食管癌细胞增殖、诱导其凋亡,并且其诱导凋亡的作用机制可能与促进caspase-3活化有关。Objective To investigate the effect of β-elemene on the proliferation and apoptosis of human esophageal carcinoma cell EC9706,and to explore the possible mechanisms of apoptosis induced by β-elemene. Methods Human esophageal carcinoma cell EC9706 were incubated in vitro. Cells were treated with different concentrations of β-elemene( 0、10、20、30、40、50 μg / ml) for 24 h or treated with 50 μg / ml β-elemene for 0,6,12 and 24 h,and the proliferation of EC9706 cells was evaluated by CCK-8. EC9706 cells were treated with 50 μg / ml β-elemene for 24 h. The apoptosis were tested by flow cytometry and the activity of caspase-3 was measured by spectrophotometry. Results The proliferation of EC9706 cells was inhibited in the β-elemene in a certain range of concerntration( 0 - 50 μg / ml). With the increase of β-elemene concerntration,the proliferation of EC9706 cells was inhibited in a concerntration-dependent manner( P〈 0. 05). Compared with EC9706 cells treated in 0 hours,the proliferation of EC9706 cells was significantly decreased in 6,12 and 24 hours( P〈 0. 05). The apoptosis rate was greater when EC9706 cells were incubated in 50 μg / ml β-elemene for 24 h than that in 0 μg / ml β-elemene( P〈 0. 05). At the meantime,the activity of caspase-3 in EC9706 cells was upregulated by β-elemene. Conclusion The proliferation of EC9706 cells is inhibited by β-elemene in the concerntration-dependent and time-dependent manner. β-elemene induced apoptosis of EC9706 cells,which might be due to the activation of caspase-3.
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