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Effect of magnetic nanoparticles of Fe3O4 and 5-bromotetrandrine on reversal of multidrug resistance in K562/A02 leukemic cells

机译:磁性纳米颗粒Fe3O4和5-溴己防己碱对K562 / A02白血病细胞多药耐药性逆转的影响

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摘要

This study aims to evaluate the multidrug resistance (MDR) reversal activity by magnetic nanoparticles of Fe3O4 (MNPs-Fe3O4) and 5-bromotetrandrine (BrTet) MDR cell line K562/A02 solitarily or symphysially. The proliferation of K562 and K562/A02 cells and the cytotoxicity on peripheral blood mononuclear cells (PMBCs) were evaluated by MTT assay. Cellular accumulation of daunorubicin (DNR) was analyzed by flow cytometry. Real-time polymerase chain reaction and Western blotting analyses were performed to examine the mRNA and protein levels of mdr1, respectively. The results showed that the combination of MNPs-Fe3O4 and BrTet with effective concentrations significantly increased cytotoxicity against MDR cell line K562/A02. Both BrTet and MNPs-Fe3O4 increased the intracellular DNR accumulation in the K562/A02 cell line, and downregulated the level of mdr1 gene and expression of P-glycoprotein. Furthermore, the combination did not have significant cytotoxicity in PMBCs. We propose that MNPs-Fe3O4 conjugated with DNR and BrTet probably have synergetic effects on MDR reversal.
机译:这项研究旨在评估磁性纳米颗粒Fe3O4(MNPs-Fe3O4)和5-溴粉防己碱(BrTet)MDR细胞系K562 / A02的多药耐药性(MDR)逆转活性。通过MTT法评估K562和K562 / A02细胞的增殖以及对外周血单个核细胞(PMBC)的细胞毒性。通过流式细胞仪分析柔红霉素(DNR)的细胞积累。进行实时聚合酶链反应和蛋白质印迹分析以分别检查mdr1的mRNA和蛋白质水平。结果表明,有效浓度的MNPs-Fe3O4和BrTet的组合显着增加了对MDR细胞株K562 / A02的细胞毒性。 BrTet和MNPs-Fe3O4均可增加K562 / A02细胞系中细胞内DNR的积累,并下调mdr1基因的水平和P-糖蛋白的表达。此外,该组合在PMBC中没有明显的细胞毒性。我们建议与DNR和BrTet结合的MNPs-Fe3O4可能对MDR逆转具有协同作用。

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