Zheng Jing, Asakawa Tetsuya, Chen Yingyu, Zheng Zhihong, Chen Buyuan, Lin Minhui, Liu Tingbo, Hu Jianda
Fujian Institute of Hematology, Fujian Provincial Key Laboratory on Hematology, Fujian Medical University Union Hospital, Fuzhou, China.
Department of Neurosurgery, Hamamatsu University School of Medicine, Handayama, Hamamatsu-city, Shizuoka, Japan.
Cell Physiol Biochem. 2017;43(1):419-430. doi: 10.1159/000480420. Epub 2017 Aug 31.
BACKGROUND/AIMS: The present study was designed to investigate the expression of multidrug resistance (MDR)-related genes, verify the synergistic effects of baicalin and Adriamycin (ADM) and investigate the related mechanisms in ADM-resistant leukaemic HL-60/ADM cells.
We used a HL-60/ADM cell line. Cytotoxicity and flow cytometry assays were employed to verify the cytotoxic effects of baicalin. Real-time polymerase chain reaction and Western blotting assays were used to assess the expression of MDR-related genes and the changes in gene expression (both MDR-related and PI3K/Akt pathway-related) induced by administration of baicalin.
We found that only multidrug resistance protein 1 (MRP1), lung resistance-related protein (LRP) and Bcl-2 genes were expressed in both HL-60 and HL-60/ADM cells. HL-60/ADM cells exhibited significantly higher expression (p < 0.05). We also observed that low-dose baicalin (5 and 10 µmol/L) can induce growth inhibition and apoptotic effects on HL-60/ADM cells by increasing the intracellular accumulation of ADM. The synergistic effect of baicalin and ADM was verified. Concerning the potential mechanisms involved in this process, we showed that baicalin down-regulated the expression of several MDR-related and PI3K/Akt pathway-related genes.
We confirmed the increased expression of MRP1, LRP and Bcl-2 genes in HL-60/ADM cells compared to regular HL-60 cells, which are recommended for future investigation on MDR. The present study provided evidence of the synergistic effect of baicalin and ADM in HL-60/ADM cells. Therefore, baicalin may be considered as a potential therapeutic agent against resistant leukaemia. Suppression of the PI3K/Akt signalling pathway, followed by inhibition of the expression of MDR-related genes may be a common mechanism in combination treatments with ADM for the reduction of resistance to ADM.
背景/目的:本研究旨在探讨多药耐药(MDR)相关基因的表达,验证黄芩苷与阿霉素(ADM)的协同作用,并研究其在ADM耐药白血病HL-60/ADM细胞中的相关机制。
我们使用了HL-60/ADM细胞系。采用细胞毒性和流式细胞术检测来验证黄芩苷的细胞毒性作用。运用实时聚合酶链反应和蛋白质免疫印迹法检测来评估MDR相关基因的表达以及黄芩苷给药后基因表达(包括MDR相关和PI3K/Akt途径相关)的变化。
我们发现多药耐药蛋白1(MRP1)、肺耐药相关蛋白(LRP)和Bcl-2基因在HL-60和HL-60/ADM细胞中均有表达。HL-60/ADM细胞的表达显著更高(p<0.05)。我们还观察到低剂量黄芩苷(5和10μmol/L)可通过增加ADM在细胞内的蓄积,对HL-60/ADM细胞产生生长抑制和凋亡作用。验证了黄芩苷与ADM的协同作用。关于这一过程涉及的潜在机制,我们表明黄芩苷下调了多个MDR相关和PI3K/Akt途径相关基因的表达。
我们证实与正常HL-60细胞相比,HL-60/ADM细胞中MRP1、LRP和Bcl-2基因的表达增加,这为未来MDR研究提供了方向。本研究提供了黄芩苷与ADM在HL-60/ADM细胞中协同作用的证据。因此,黄芩苷可被视为一种潜在的抗耐药白血病治疗药物。抑制PI3K/Akt信号通路,随后抑制MDR相关基因的表达,可能是与ADM联合治疗降低对ADM耐药性的共同机制。