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五味子醇甲逆转耐药慢性髓性白血病细胞K562/A02中的多药耐药性。

Schizandrol A reverses multidrug resistance in resistant chronic myeloid leukemia cells K562/A02.

作者信息

Arken Nurguli

出版信息

Cell Mol Biol (Noisy-le-grand). 2019 Jan 31;65(1):78-83.

Abstract

Overexpression of P-gp is the main cause of multidrug resistance (MDR) and chemotherapeutic failure in leukemia. In this study, the multidrug resistance reverse effect of Schizandrol A (SchA) was demonstrated with P-gp overexpressed drug-resistant K562/A02 cells. SchA had almost no cytotoxic activity, the EC50 value reversed to DOX was in the nanomole range of (707 ± 29nM) and had a high selectivity index (> 113) to normal cells. DOX accumulation and Rh123 efflux tests demonstrated that the MDR reversal activity of SchA was induced by inhibiting P-gp function. Western blotting assay showed that SchA down-regulated the expression of P-gp by inhibiting the PI3K / Akt signaling pathway, which was also a key factor in reversal activity. Therefore, SchA may be a potential candidate for natural MDR reversal agents.

摘要

P-糖蛋白的过表达是白血病多药耐药(MDR)和化疗失败的主要原因。在本研究中,使用P-糖蛋白过表达的耐药K562/A02细胞证明了五味子醇甲(SchA)的多药耐药逆转作用。SchA几乎没有细胞毒性活性,对阿霉素(DOX)的EC50值逆转至纳摩尔范围(707±29nM),对正常细胞具有高选择性指数(>113)。DOX蓄积和罗丹明123外排试验表明,SchA的MDR逆转活性是通过抑制P-糖蛋白功能诱导的。蛋白质免疫印迹分析表明,SchA通过抑制PI3K/Akt信号通路下调P-糖蛋白的表达,这也是逆转活性的关键因素。因此,SchA可能是天然MDR逆转剂的潜在候选物。

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