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去甲斑蝥素对白血病细胞系K562的增殖、凋亡、细胞周期及NF-κB活性的影响

姚铠涛,陈江声,陈春莉   

  1. 汕头大学医学院第二附属医院血液肿瘤科
  • 收稿日期:2015-03-06 修回日期:2015-03-27 出版日期:2015-05-31 发布日期:2015-05-31

Effect of norcantharidin on the proliferation, apoptosis, cell cycle and activity of NF-κB on human leukemia cell line K562

YAO Kaitao, CHEN Jiangsheng, CHEN Chunli.   

  1. the Second Affiliated Hospital of Shantou University Medical College
  • Received:2015-03-06 Revised:2015-03-27 Online:2015-05-31 Published:2015-05-31

摘要: 目的 探讨去甲斑蝥素(NCTD)对白血病细胞系K562的增殖、凋亡、细胞周期及核因子(NF)-κB活性的影响。方法 采用CCK-8试剂盒检测不同浓度NCTD(0、10、25、50、100 μmol/L)处理K562细胞24、48、72、96 h后的增殖抑制率,采用流式细胞术检测不同浓度NCTD处理24、48 h后的细胞凋亡率和处理48 h后的细胞周期,采用原位细胞凋亡检测试剂盒(Tunnel)检测不同浓度NCTD处理24、48 h后的细胞凋亡指数,采用Western blotting检测不同浓度NCTD处理48 h后的NF-κB p65及IκBα水平以评价NF-κB活性的变化。结果 在10~100 μmol/L范围内,NCTD可呈时间和浓度依赖的方式升高K562细胞的增殖抑制率,各浓度间的差异有统计学意义(P<0.05);与0 μmol/L相比,其余各浓度处理24、48 h后的凋亡率和凋亡指数均升高,处理48 h后的G0/G1期细胞比例升高,S、G2/M期细胞比例均降低,NF-κB p65水平降低,IκB-α水平升高,以上差异均有统计学意义(P<0.05)。结论 NCTD对白血病细胞系K562有细胞毒性,可抑制该细胞的增殖、诱导其凋亡及细胞周期阻滞并下调NF-κB表达。

Abstract: Objective To investigate the effect of norcantharidin (NCTD) on proliferation, apoptosis, cell cycle and the activity of nuclear factor (NF)κB on human leukemia cell line K562. Methods The K562 cell was treated with different concentrations of NCTD (0, 10, 25, 50, 100 μmol/L) and the proliferation inhibition rates were measured by CCK-8 kit at 24, 48, 72, 96 h post-treatment. The apoptotic rates at 24 and 48 h together with cell cycle at 48 h after NCTD treatments were evaluated via flow cytometry. The in situ cell death detection kit (Tunnel) was applied to measure the levels of apoptosis at 24 and 48 h post-treatment. As for the activity of NF-κB, levels of p65 subunit of NFκB and IκBα were detected by Western blotting at 48 h posttreatment. Results NCTD in the range 10 to 100 μmol/L could increase the proliferation inhibition rates on K562 cells in a dose- and time- dependent manner (P<0.05). In comparison with 0 μmol/L NCTD, there were elevated apoptotic rates and indices at 24 and 48 h posttreatment (P<0.05). The treatment with NCTD (10~100 μmol/L) resulted in a higher proportion of cells within G0/G1phase but a lower proportion of cells within S and G2/M phases with significant differences than 0 μmol/L (P<0.05). Reduced IκBα but elevated p65 subunit of NFκB were observed only in 10100 μmol/L NCTD (P<0.05).
Conclusion NCTD exhibited cytotoxity on K562 cells, possibly by the inhibition of the cell proliferation, induction of apoptosis and down-regulation of the activity of NF-κB.

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