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首页> 外文期刊>Bulgarian journal of veterinary medicine. >Ivanova, D., Z. Yaneva, R. Bakalova, S. Semkova & Zh. Zhelev, 2021. The antimalaria drug artemisinin displays strong cytotoxic effect on leukaemia lymphocytes in combination with vitamin C and pro-vitamin K3. Bulg. J. Vet. Med., 24, No 4, 533-543
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Ivanova, D., Z. Yaneva, R. Bakalova, S. Semkova & Zh. Zhelev, 2021. The antimalaria drug artemisinin displays strong cytotoxic effect on leukaemia lymphocytes in combination with vitamin C and pro-vitamin K3. Bulg. J. Vet. Med., 24, No 4, 533-543

机译:Ivanova,D.,Z. Yaneva,R.Bakalova,S. Semkova& Zh。 Zhelev,2021. Antimalaria药物青蒿素对白血病淋巴细胞的强烈细胞毒性作用与维生素C和亲 - 维生素K3组合。 灯泡。 J. Vet。 Med。,24,4,533-543

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This study investigated the anticancer effect of the anti-parasitic drug artemisinin in combination with two redox modulators: vitamin C and pro-vitamin K3 (C/K3) The experiments were conducted on leukaemia cells Jurkat. Cells were treated with either artemisinin or C/K3 alone and with all three compounds. Cell proliferation and viability were analysed using trypan blue stating and automated cell counting. The results showed that artemisinin (>10 mM) suppressed cell proliferation activity, but did not induce cell death up to 500 mM. The drug demonstrated a clear cytostatic effect at concentrations 250- 500 mM – Jurkat cells did not proliferate, but were alive. The combination C/K3 (200:2, 300:3 mM/mM) applied alone did not affect cell proliferation and viability. Vitamins C/K3 in concentration ratio 500:5 (μM/mM) decreased cell proliferation activity by ~10%. The triple combination artemisinin/C/K3 manifested synergistic anti-proliferative effects at all concentration ratios analysed. This synergistic effect increased with increasing C/K3 concentration. Based on literature data, it was assumed that the anti-proliferative effect of the triple combination was mediated by changes in the redox-homeostasis of cancer cells. The C/K3 redox system likely acted on cancer mitochondria and increased superoxide production and activation of pro-apoptotic signals, specific for cancer cells. On the other hand, artemisinin could generate hydroxyl radicals as a result of activation of Fenton reactions, depleting intracellular reducing equivalents. Both redox mechanisms lead to activation of signal pathways for induction of cancer cell death.
机译:本研究研究了抗寄生药物氨化蛋白与两种氧化还原调节剂组合的抗癌效果:维生素C和亲 - 维生素K3(C / K3)在白血病细胞Jurkat进行实验。单独用氨化蛋白酶或C / K3和所有三种化合物处理细胞。使用台盼蓝说明和自动细胞计数分析细胞增殖和活力。结果表明,青蒿素(> 10mm)抑制细胞增殖活性,但未诱导细胞死亡高达500毫米。该药物在浓度的浓度下阐明了澄清的细胞抑制效果 - Jurkat细胞未增殖,但活着。单独施用的C / K3(200:2,300:3mm / mm)的组合不影响细胞增殖和活力。浓度比500:5(μm/ mm)的维生素C / K3降低细胞增殖活性〜10%。三重组合青蒿素/ C / K3在分析的所有浓度比下表现出协同抗增殖效果。随着C / K3浓度的增加,这种协同效应增加。基于文献数据,假设三重组合的抗增殖效应是通过癌细胞的氧化还原性稳态的变化介导的。 C / K3氧化还原系统可能作用于癌症线粒体和增加的超氧化物生产和激活促凋亡信号,对癌细胞特异。另一方面,由于活顿反应的激活,耗尽细胞内还原等同物,阿尔胺蛋白可以产生羟基自由基。氧化还原机制均导致激活信号途径以诱导癌细胞死亡。

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