首页> 外文期刊>Chemico-biological interactions >Natural antioxidants synergistically enhance the anticancer potential of AP9-cd, a novel lignan composition from Cedrus deodara in human leukemia HL-60 cells.
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Natural antioxidants synergistically enhance the anticancer potential of AP9-cd, a novel lignan composition from Cedrus deodara in human leukemia HL-60 cells.

机译:天然抗氧化剂协同增强AP9-cd的抗癌潜力,AP9-cd是一种来自雪松(Cedrus deodara)的新型木脂素组合物,可用于人类白血病HL-60细胞。

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摘要

Antioxidants have been used as adjuvant with anticancer therapy to synergize the potential of the anti-neoplastic therapeutics. Based on the fact, we have studied the effect of three natural antioxidants curcumin, silymarin and acteoside on AP9-cd (standardized lignan composition from Cedrus deodara) induced cytotoxicity in human leukemia HL-60 cells. The antioxidant potential of individual test compounds was first evaluated with ferric reducing antioxidant power (FRAP) test, which revealed that all four molecules behave as antioxidants. The apoptotic potential of AP9-cd was significantly enhanced in HL-60 cells in the presence of curcumin, silymarin and acteoside. It was confirmed by using various models like MTT assay, DNA fragmentation, nuclei condensation, sub-Go DNA population, Annexin-V-FITC binding, ROS depletion and immunoblotting in HL-60 cells. AP9-cd and individual antioxidants alone at low doses (10mug and 10muM, respectively) have meager or no cytotoxicity in HL-60 cells, whereas in mutual combinations, there were 2-3 times enhancement in Annexin-V-FITC and sub-Go DNA population. Moreover, prominent DNA ladders were observed at low doses of AP9-cd in combinations with various antioxidants. The Hoechst staining of the nucleus also revealed the same results for the HL-60 cells treated with AP9-cd and different antioxidants. The molecular diagnostics revealed that the combinations induced a strong antioxidant effect which was correlated with the downregulation of NF-kappaB expression in the nucleus. Out of the three antioxidants, curcumin was found to be more potent than acteoside and silymarin in terms of enhancing the apoptotic potential of AP9-cd. These results propose an important role of natural antioxidant as adjuvant to enhance the anticancer potential of AP9-cd and more likely other anti-neoplastic therapeutics.
机译:抗氧化剂已被用作抗癌治疗的佐剂,以协同抗肿瘤治疗的潜力。基于这一事实,我们研究了三种天然抗氧化剂姜黄素,水飞蓟素和Acteoside对AP9-cd(雪松的标准化木脂素成分)诱导的人白血病HL-60细胞的细胞毒性作用。首先通过三价铁还原抗氧化剂能力(FRAP)测试来评估单个测试化合物的抗氧化剂潜力,该结果表明所有四个分子均具有抗氧化剂的作用。在姜黄素,水飞蓟素和Acteoside的存在下,HL-60细胞中AP9-cd的凋亡潜力显着增强。通过使用各种模型进行了证实,例如MTT分析,DNA片段化,核浓缩,sub-Go DNA群体,膜联蛋白-V-FITC结合,ROS耗竭和HL-60细胞的免疫印迹。低剂量(分别为10mug和10μM)时,单独的AP9-cd和单独的抗氧化剂在HL-60细胞中几乎没有或没有细胞毒性,而在相互结合时,膜联蛋白-V-FITC和sub-Go的增强作用是2-3倍DNA种群。此外,在低剂量的AP9-cd与各种抗氧化剂的组合中观察到了显着的DNA阶梯。核的Hoechst染色也显示了用AP9-cd和不同的抗氧化剂处理的HL-60细胞具有相同的结果。分子诊断表明,这些组合物诱导了强烈的抗氧化作用,这与细胞核中NF-κB表达的下调有关。在三种抗氧化剂中,姜黄素在增强AP9-cd的凋亡潜力方面比acteoside和水飞蓟素更有效。这些结果表明,天然抗氧化剂作为佐剂的重要作用是增强AP9-cd的抗癌潜力,以及其他可能的抗肿瘤疗法。

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