Inhibitory Effect of Ouabain on Resistance to Imatinib in Chronic Myeloid Leukemia K562/G01 Cells

IF 0.4 4区 医学 Q4 PHARMACOLOGY & PHARMACY Indian Journal of Pharmaceutical Sciences Pub Date : 2023-01-01 DOI:10.36468/pharmaceutical-sciences.1129
Chang-Quan Sun, J. Liu, Shiqi Zhai, H. Liu, L. Peng, Jing Hu
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Abstract

Ouabain has shown powerful anti-proliferation activities in various cancers, but its effect on imatinib-resistant chronic myeloid leukemia and toxicity on normal mice has not been investigated. Cell Counting Kit-8 assay was used to detect cytotoxicity and reversal effect of ouabain with different concentration (0.01 µM, 0.1 µM, 1.0 µM, 10 µM) on drug resistance of imatinib-resistant cell line of chronic myeloid leukemia (K562/G01 cell line). Flow cytometry was used to detect the apoptosis effect and cell cycle arrest. Hematological examination, biochemical examination and histological examination were used to detect sub-chronic toxicity of ouabain on healthy mice. In our present study, ouabain showed greatly inhibitory effect and significantly reduced half minimal inhibitory concentration of imatinib in K562/ G01 cells, an imatinib-resistant cell line of chronic myeloid leukemia, in a dose-and time-dependent manner, which implied that ouabain increased cell sensitivity to imatinib. Ouabain enhanced apoptosis induced by imatinib in K562/G01 cells not through cell cycle arrest. Animal experiments showed that there were no significant variances in hematological, liver function, kidney function parameters and organ histopathology of all mice groups. These data suggested that ouabain could be a potential agent to treat imatinib-resistant chronic myeloid leukemia for its powerful cytotoxicity as well as reversal effect, but further study is needed to find out its specific mechanism.
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瓦巴因对慢性髓系白血病K562/G01细胞对伊马替尼耐药的抑制作用
瓦巴因在多种癌症中显示出强大的抗增殖活性,但其对伊马替尼耐药慢性髓系白血病的作用和对正常小鼠的毒性尚未研究。采用细胞计数试剂盒-8检测不同浓度(0.01µM、0.1µM、1.0µM、10µM)的瓦巴因对慢性髓系白血病伊马替尼耐药细胞株(K562/G01细胞株)耐药的细胞毒性及逆转作用。流式细胞术检测细胞凋亡效应和细胞周期阻滞。采用血液学检查、生化检查和组织学检查检测乌阿巴因对健康小鼠的亚慢性毒性。在本研究中,瓦巴因对慢性髓性白血病耐伊马替尼细胞系K562/ G01细胞表现出明显的抑制作用,显著降低伊马替尼最低抑制浓度的一半,且呈剂量和时间依赖关系,表明瓦巴因增加了细胞对伊马替尼的敏感性。瓦巴因增强伊马替尼诱导的K562/G01细胞凋亡,但不通过细胞周期阻滞。动物实验结果显示,各组小鼠血液学、肝功能、肾功能参数及器官组织病理学均无显著差异。这些数据提示,瓦巴因具有强大的细胞毒性和逆转作用,可能成为治疗伊马替尼耐药慢性髓系白血病的潜在药物,但其具体机制有待进一步研究。
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期刊介绍: The Indian Journal of Pharmaceutical Sciences (IJPS) is a bi-monthly Journal, which publishes original research work that contributes significantly to further the scientific knowledge in Pharmaceutical Sciences (Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy and Phytochemistry, Pharmacology and Therapeutics, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Pharmacovigilance, Pharmacoepidemiology, Pharmacoeconomics, Drug Information, Patient Counselling, Adverse Drug Reactions Monitoring, Medication Errors, Medication Optimization, Medication Therapy Management, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest). The Journal publishes original research work either as a Full Research Paper or as a Short Communication. Review Articles on current topics in Pharmaceutical Sciences are also considered for publication by the Journal.
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