芬苯达唑联合紫杉醇对HL-60细胞的抗癌作用

Jihye Sung, H. Joo
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引用次数: 1

摘要

芬苯达唑(FBZ)是最安全的驱虫药之一。人们发现FBZ通过破坏微管的稳定而具有抗癌作用。本研究研究了微管稳定抗癌药物紫杉醇(PA)与FBZ对人白血病HL-60细胞的协同作用。3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化铵染色和Hoechst 33342染色结果显示,FBZ和PA处理后细胞代谢活性显著降低,细胞核形态明显改变。为了研究活性氧(ROS)的参与,我们测量了n -乙酰- l-半胱氨酸(NAC)处理后细胞的代谢活性。事实上,NAC显著增加了FBZ和PA处理的细胞的代谢活性,表明这两种药物至少部分通过ROS影响。此外,在膜联蛋白V-异硫氰酸荧光素/碘化丙啶染色试验中,FBZ和PA增加了细胞死亡。综上所述,FBZ和PA在一定浓度下对HL-60细胞具有协同抗癌活性。这些结果可能为癌症相关领域的研究人员和临床医生提供一些有价值的信息,以扩大FBZ的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-cancer effects of Fenbendazole and Paclitaxel combination on HL-60 cells
Fenbendazole (FBZ) is one of the safest anthelmintic drugs. FBZ has been found to have anti-cancer effects by destabilizing microtubules. In this study, a synergistic effect of paclitaxel (PA), a microtubule-stabilizing anti-cancer agent, and FBZ was investigated on HL-60 cells, a human leukemia cell line. The metabolic activity of cells significantly decreased and the nucleus morphology upon the treatment of FBZ and PA based on 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide assay and Hoechst 33342 staining, respectively. To investigate the involvement of reactive oxygen species (ROS), the metabolic activity of the cells after treatment of N-acetyl-L-cysteine (NAC) was measured. Indeed, NAC significantly increased the metabolic activity of the cells treated with FBZ and PA, suggesting that both drugs affect at least in part via ROS. Furthermore, FBZ and PA increased cell death in an annexin V- fluorescein isothiocyanate/propidium iodide staining assay. Taken together, FBZ and PA have a synergistic anti-cancer activity on HL-60 cells at a certain concentration. These results may provide researchers and clinicians in cancer-related fields with some valuable information to broaden the use of FBZ.
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