丁岩, 何丽容, 曹卡加, 陆豫, 古练权, 符立梧. 叠氮甲基蒽醌衍生物诱导KB细胞及其耐药株细胞的凋亡J. 药学学报, 2005, 40(1): 22-26.
引用本文: 丁岩, 何丽容, 曹卡加, 陆豫, 古练权, 符立梧. 叠氮甲基蒽醌衍生物诱导KB细胞及其耐药株细胞的凋亡J. 药学学报, 2005, 40(1): 22-26.
DING Yan, HE Li-rong, CAO Ka-jia, LU Yu, GU Lian-quan, FU Li-wu. Apoptosis of human carcinoma of mouth floor KB cells and multidrug resistant KBv200 cells induced by azide methyl anthraquinone derivativeJ. Acta Pharmaceutica Sinica, 2005, 40(1): 22-26.
Citation: DING Yan, HE Li-rong, CAO Ka-jia, LU Yu, GU Lian-quan, FU Li-wu. Apoptosis of human carcinoma of mouth floor KB cells and multidrug resistant KBv200 cells induced by azide methyl anthraquinone derivativeJ. Acta Pharmaceutica Sinica, 2005, 40(1): 22-26.

叠氮甲基蒽醌衍生物诱导KB细胞及其耐药株细胞的凋亡

Apoptosis of human carcinoma of mouth floor KB cells and multidrug resistant KBv200 cells induced by azide methyl anthraquinone derivative

  • 摘要: 目的研究大黄素的蒽醌衍生物6-叠氮甲基-1-羟基-3,8-二甲氧基-9,10-蒽醌(AMAD-10)抑制KB细胞及其耐药株KBv200的生长和诱导细胞凋亡的作用。方法细胞毒用MTT法测定;细胞内活性氧(ROS)和线粒体跨膜电位(ΔΨm)分别用DCFH-DA和DiOC6荧光探针标记,流式细胞仪检测;Annexin V染色和DNA琼脂糖凝胶电泳检测AMAD诱导凋亡作用。结果AMAD浓度依赖性抑制KB和KBv200细胞的生长和引起活性氧明显增加,并能引起两种细胞ΔΨm时间依赖性的降低,AMAD可浓度依赖性地诱导两种细胞凋亡。结论AMAD体外显著抑制KB及其耐药株KBv200的生长,这可能与其引起细胞内ROS增加、使ΔΨm降低,从而诱导细胞凋亡有关。

     

    Abstract: AimTo determine the effects of azide methyl anthraquinone derivative (AMAD) on growth inhibition and inducing apoptosis of multidrug resistant (MDR) KBv200 cells and parental drug-sensitive KB cells. MethodsCytotoxicity was determined by tetrazolium (MTT) assay. Reactive oxygen species (ROS) levels and mitochondrial membrane potential (ΔΨm) in cells were labeled with DCFH-DA and DiOC6 and tested by flow cytometry. Annexin V stain and DNA ladder were used to examine the apoptosis of KB and KBv200 cells induced by AMAD. ResultsAMAD was shown to inhibit the growth of KB and KBv200 cells significantly in a concentration-dependent manner, with mean IC50 of 0.36 and 0.45 μmol·L-1, respectively. The generation of ROS increased obviously after the cells were treated with AMAD for 12 h, up to the peak in 24 h, meanwhile the levels of ΔΨm were time-dependently decreased. DNA fragmentation appeared on the agarose gel. Annexin V stain showed AMAD induced apoptosis of KB and KBv200 cells also in a concentration-dependent manner. ConclusionAMAD showed inhibitory effect on both MDR KBv200 cells and parental drug-sensitive KB cells. The mechanism of action was associated with the increase of the cellular ROS level and the decrease of the mitochondrial membrane potential induced by AMAD, which result in cell apoptosis.

     

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