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首页> 外文期刊>Acta Veterinaria Hungarica >IN VITRO EFFECTS OF DOXORUBICIN AND DERACOXIB ON OXIDATIVE-STRESS-RELATED PARAMETERS IN CANINE MAMMARY CARCINOMA CELLS
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IN VITRO EFFECTS OF DOXORUBICIN AND DERACOXIB ON OXIDATIVE-STRESS-RELATED PARAMETERS IN CANINE MAMMARY CARCINOMA CELLS

机译:阿霉素和德拉索昔对犬乳癌细胞氧化应激相关参数的体外影响

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摘要

The present study evaluated the effects of doxorubicin (DOX) and deracoxib (DER), as single agents and in combination treatments, on antioxidant parameters in the canine mammary carcinoma cell line CMT-U27. The cells were exposed to DOX and DER for 24, 48 and 72 h. The viability and malondialdehyde (MDA), nitric oxide (NO), catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GSHPx) and total glutathione (GSH) activities of CMT-U27 cells were determined. The half inhibition concentration (IC50) of DOX was found to be similar to 0.9 mu M in the 72-h period. IC50 and 1/10 IC50 concentrations of DOX were combined with all concentrations of DER (50-1000 mu M) in the combination experiments. The results showed increased oxidative status associated with significant decreases of CAT and GSH levels in CMT-U27 cells exposed to 10-mu M and higher concentrations of DOX compared to control cells. In contrast, there were no significant changes in the groups tested with any of the concentrations of DER (50-1000 mu M). In combination treatments, DER attenuated DOX-induced oxidative damage by modulating the enzymatic and non-enzymatic components in CMT-U27 cells. We suggest that the combination of DOX and DER can be beneficial in the treatment of cancer cells by increasing cellular responses to oxidative stress. In conclusion, the use of COX inhibitor in conjunction with a chemotherapeutic agent may provide a basis for new concepts of cancer treatment through systematic modulation of the antioxidant defence systems in mammary cancers of animals
机译:本研究评估了阿霉素(DOX)和德拉考昔(DER)作为单药和联合治疗对犬乳腺癌细胞CMT-U27中抗氧化剂参数的影响。将细胞暴露于DOX和DER 24、48和72小时。测定了CMT-U27细胞的活力和丙二醛(MDA),一氧化氮(NO),过氧化氢酶(CAT),超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSHPx)和总谷胱甘肽(GSH)活性。发现在72小时内,DOX的半数抑制浓度(IC50)类似于0.9μM。在结合实验中,将IC50和1/10 IC50浓度的DOX与所有浓度的DER(50-1000μM)混合。结果表明,与对照细胞相比,在暴露于10μM的CMT-U27细胞和较高浓度的DOX中,氧化状态增加与CAT和GSH水平的显着降低有关。相比之下,使用任何浓度的DER(50-1000μM)进行测试的组均无明显变化。在联合治疗中,DER通过调节CMT-U27细胞中的酶和非酶成分来减轻DOX诱导的氧化损伤。我们建议,通过增加细胞对氧化应激的反应,DOX和DER的组合可以有益于治疗癌细胞。总之,将COX抑制剂与化学治疗剂结合使用可通过系统调节动物乳癌中的抗氧化剂防御系统,为癌症治疗的新概念提供基础

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