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首页> 外文期刊>Journal of experimental & clinical cancer research : >Reactive oxygen species-mediated apoptosis contributes to chemosensitization effect of saikosaponins on cisplatin-induced cytotoxicity in cancer cells
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Reactive oxygen species-mediated apoptosis contributes to chemosensitization effect of saikosaponins on cisplatin-induced cytotoxicity in cancer cells

机译:活性氧介导的细胞凋亡有助于皂苷对顺铂诱导的癌细胞毒性的化学增敏作用

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Background Saikosaponin-a and -d, two naturally occurring compounds derived from Bupleurum radix, have been shown to exert anti-cancer activity in several cancer cell lines. However, the effect of combination of saikosaponins with chemotherapeutic drugs has never been addressed. Thus, we investigated whether these two saikosaponins have chemosensitization effect on cisplatin-induced cancer cell cytotoxicity. Methods Two cervical cancer cell lines, HeLa and Siha, an ovarian cancer cell line, SKOV3, and a non-small cell lung cancer cell line, A549, were treated with saikosaponins or cisplatin individually or in combination. Cell death was quantitatively detected by the release of lactate dehydrogenase (LDH) using a cytotoxicity detection kit. Cellular ROS was analyzed by flow cytometry. Apoptosis was evaluated by AO/EB staining, flow cytometry after Anexin V and PI staining, and Western blot for caspase activation. ROS scavengers and caspase inhibitor were used to determine the roles of ROS and apoptosis in the effects of saikosaponins on cisplatin-induced cell death. Results Both saikosaponin-a and -d sensitized cancer cells to cisplatin-induced cell death in a dose-dependent manner, which was accompanied with induction of reactive oxygen species (ROS) accumulation. The dead cells showed typical apoptotic morphologies. Both early apoptotic and late apoptotic cells detected by flow cytometry were increased in saikosaponins and cisplatin cotreated cells, accompanied by activation of the caspase pathway. The pan-caspase inhibitor z-VAD and ROS scanvengers butylated hydroxyanisole (BHA) and N-acetyl-L-cysteine (NAC) dramatically suppressed the potentiated cytotoxicity achieved by combination of saikosaponin-a or -d and cisplatin. Conclusions These results suggest that saikosaponins sensitize cancer cells to cisplatin through ROS-mediated apoptosis, and the combination of saikosaponins with cisplatin could be an effective therapeutic strategy.
机译:背景技术柴胡皂苷-a和-d是两种来自柴胡的天然存在的化合物,已显示出在几种癌细胞系中发挥抗癌活性。然而,从未将皂苷皂苷与化学治疗药物组合的作用。因此,我们研究了这两种皂苷对顺铂诱导的癌细胞的细胞毒性是否具有化学增敏作用。方法分别用柴胡皂苷或顺铂对两种宫颈癌细胞系HeLa和Siha,卵巢癌细胞系SKOV3和非小细胞肺癌细胞系A549进行处理。使用细胞毒性检测试剂盒通过释放乳酸脱氢酶(LDH)定量检测细胞死亡。通过流式细胞术分析细胞ROS。通过AO / EB染色,Anexin V和PI染色后的流式细胞仪以及胱天蛋白酶激活的Western印迹来评估细胞凋亡。使用ROS清除剂和caspase抑制剂来确定ROS和细胞凋亡在皂苷对顺铂诱导的细胞死亡中的作用。结果saikosaponin-a和-d均以剂量依赖性方式使癌细胞对顺铂诱导的细胞死亡敏感,并伴随着活性氧(ROS)的积累。死细胞显示出典型的凋亡形态。流式细胞术检测到的早期凋亡和晚期凋亡细胞在皂苷和顺铂共处理的细胞中均增加,并伴有半胱天冬酶途径的激活。泛半胱天冬酶抑制剂z-VAD和ROS毒杀了丁基羟基茴香醚(BHA)和N-乙酰基-L-半胱氨酸(NAC),从而极大地抑制了皂苷-a或-d与顺铂组合所产生的增强的细胞毒性。结论这些结果表明,皂苷皂苷通过ROS介导的细胞凋亡使癌细胞对顺铂敏感,而皂苷皂苷与顺铂的组合可能是一种有效的治疗策略。

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