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白藜芦醇通过调控 PI3K/Akt/Nrf2 信号通路逆转 HL-60/ADR 细胞多药耐药性

Involvement of the PI3K/Akt/Nrf2 Signaling Pathway in Resveratrol-Mediated Reversal of Drug Resistance in HL-60/ADR Cells.

机构信息

a Department of Clinical Laboratory , The Second Hospital of Hebei Medical University , Shijiazhuang , Hebei, China.

b Legacy Health and Cascade Pathology Services , Portland , Oregon, USA.

出版信息

Nutr Cancer. 2019;71(6):1007-1018. doi: 10.1080/01635581.2019.1578387. Epub 2019 Apr 29.

Abstract

Resistance to chemotherapy drugs, such as adriamycin (ADR), is a common problem in acute myeloid leukemia (AML) patients. We hypothesized that the natural compound resveratrol (Res) may reverse AML drug resistance through the PI3K/Akt/Nrf2 pathway. We investigated the in vitro effect of Res using human promyelocytic leukemia cells (HL-60) and the ADR-resistant cell line (HL-60/ADR) and treated with either Res or ADR + Res. Cellular proliferation inhibition rate, auto-fluorescence intensity of ADR in HL-60/ADR cells and HL-60 cells, mRNA expression of and the drug-resistant gene , and protein expression of PI3K, Akt, p-Akt, Nrf2, and MRP1 were measured. Results showed ADR + Res had a more significant inhibitory effect than ADR alone on HL-60/ADR cells. Auto-fluorescence intensity of ADR in HL-60/ADR cells treated with ADR + Res significantly increased. No difference of the auto-fluorescence intensity of ADR was observed in HL-60 cells treated with ADR and ADR + Res. mRNA expression of and significantly decreased in HL-60/ADR cells treated with both Res and ADR + Res; protein expression of PI3K, p-Akt, Nrf2, and MRP1 significantly decreased in HL-60/ADR cells treated with PI3K inhibitor, Res and ADR + Res. In conclusion, Res reverses the drug resistance of AML HL-60/ADR cells through regulation of the PI3K/Akt/Nrf2 signaling pathway and MRP1 expression.

摘要

化疗药物耐药,如阿霉素(ADR),是急性髓系白血病(AML)患者的常见问题。我们假设天然化合物白藜芦醇(Res)可能通过 PI3K/Akt/Nrf2 通路逆转 AML 耐药性。我们使用人早幼粒细胞白血病细胞(HL-60)和 ADR 耐药细胞系(HL-60/ADR)研究了 Res 的体外作用,并分别用 Res 或 ADR+Res 处理。测量 HL-60/ADR 细胞和 HL-60 细胞中 ADR 的细胞增殖抑制率、自荧光强度、和耐药基因 的 mRNA 表达,以及 PI3K、Akt、p-Akt、Nrf2 和 MRP1 的蛋白表达。结果表明,与单独使用 ADR 相比,ADR+Res 对 HL-60/ADR 细胞的抑制作用更显著。ADR+Res 处理的 HL-60/ADR 细胞中 ADR 的自荧光强度明显增加。而 ADR 和 ADR+Res 处理的 HL-60 细胞中,ADR 的自荧光强度没有差异。与单独使用 Res 相比,Res 和 ADR+Res 处理的 HL-60/ADR 细胞中 和 的 mRNA 表达显著降低;PI3K 抑制剂、Res 和 ADR+Res 处理的 HL-60/ADR 细胞中 PI3K、p-Akt、Nrf2 和 MRP1 的蛋白表达显著降低。结论:Res 通过调节 PI3K/Akt/Nrf2 信号通路和 MRP1 表达逆转 AML HL-60/ADR 细胞的耐药性。

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