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机构地区:[1]泰山医学院药理教研室 [2]昆明医学院药理教研室,云南昆明650031 [3]昆明重金属研究所
出 处:《泰山医学院学报》2006年第3期189-192,共4页Journal of Taishan Medical College
摘 要:目的研究乙酰水杨酸铜对HTC—116细胞生长的抑制及诱导凋亡作用,探讨其抗肿瘤作用的机制。方法采用MTT法检测乙酰水杨酸铜对HTC-116细胞的毒性作用;荧光显微镜照相及流式细胞术检测乙酰水杨酸铜诱导HTC-116细胞凋亡的作用。结果乙酰水杨酸铜处理HTC-116细胞48h、72h的IC50值分别为6.10μmol/L和4.48μmol/L;10μmol/L乙酰水杨酸铜处理HTC-116细胞24h镜下可见核分裂及凋亡小体形成,处理48h流式细胞术可检测出明显的亚二倍体峰,凋亡率达34.1%。细胞凋亡发生呈剂量和时间依赖性。结论乙酰水杨酸铜可显著抑制HTC-116细胞生长并诱导其凋亡。Objective: To study the effect of Cu( Ⅱ )2 (acetylsalicylate)4 on the inhibition of growth and the induced apeptosis in HCT-116 cells. Methods: The toxicity of Cu ( Ⅱ )2 (acetylsalicylate) 4 to HCT-116 cells was detected by MTT assay, and the effect on the induced apoptosis was detected by Fluoroscope and flow cytometer. Results: When HCT-116 ceils were treated by Cu ( Ⅱ ) 2 ( acetyl-salicylate ) 4 for 48h and 72h, the IC50 were 6. 10 μmol/L and 4. 48 μmol/L respectively. Nucleus cleavage and apoptotic bodies were observed when HCT-116 ceils were treated by Cu( Ⅱ ) 2 (acetylsalicylate)4 (10 μmol/L) for 24 h; and an obvious subdiploid peak exhibited when HCT-116 cells were treated by Cu( Ⅱ )2 (acetylsalicylate)4 (10 μmol/L) for 48 h, and the rate of apoptosis was 34.1%. Apoptosis was dependent on concentration and time. Conclusion : The results suggest that Cu ( Ⅱ ) 2 ( acetylsalicylate ) 4 can significantly inhibit the growth of HCT- 116 cells and induce the apoptosis.
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