Wang Wenjing, Niu Shubin, Qiao Luxin, Wei Feili, Yin Jiming, Wang Shanshan, Ouyang Yabo, Chen Dexi
Capital Medical University Affiliated Beijing You An Hospital, Beijing, 100069, China.
Beijing Institute of Hepatology, Beijing, 100069, China.
Biomed Res Int. 2019 Feb 11;2019:8727935. doi: 10.1155/2019/8727935. eCollection 2019.
Multidrug resistance (MDR) is a major obstacle in chemotherapy of leukemia treatments. In this paper, we investigated Usnea Acid (UA) as MDR reversal agent on hematologic K562/ADR cells via ROS dependent apoptosis.
CCK8 assay was used to measure cell viability rate of K562/ADR. Intracellular reactive oxygen species (ROS) generation, cell cycle distribution, cell apoptosis were measured with flow cytometry, respectively. Proteins related to apoptosis were measured by Western blot. Intracellular Adriamycin accumulation was observed by confocal microscopy and measured by flow cytometry.
In vitro study showed intracellular Adriamycin accumulation was remarkably increased by UA. Cell viability treated with Adr (4 M) was decreased from 89.8% ± 4.7 to 32% ± 8.9 by combined with UA (4 M). Adr-induced apoptosis and G/G phase cell cycle arrest were remarkably increased by UA, as well as, intracellular ROS level. However, MDR reversing activity of UA was inhibited by N-acetyl cysteine (NAC), a ROS scavenger.
These data provide compelling evidence that UA is a promising agent against MDR in leukemia cell line and suggest a promising therapeutic approach for leukemia.
多药耐药(MDR)是白血病治疗化疗中的主要障碍。在本文中,我们研究了松萝酸(UA)作为通过活性氧(ROS)依赖性凋亡对血液学K562/ADR细胞的多药耐药逆转剂。
采用CCK8法检测K562/ADR细胞的活力率。分别用流式细胞术检测细胞内活性氧(ROS)的产生、细胞周期分布和细胞凋亡。通过蛋白质印迹法检测与凋亡相关的蛋白质。通过共聚焦显微镜观察并通过流式细胞术测量细胞内阿霉素的积累。
体外研究表明,UA显著增加细胞内阿霉素的积累。与UA(4 μM)联合使用时,用阿霉素(4 μM)处理的细胞活力从89.8%±4.7降至32%±8.9。UA显著增加了阿霉素诱导的凋亡和G0/G1期细胞周期阻滞,以及细胞内ROS水平。然而,UA的多药耐药逆转活性被ROS清除剂N-乙酰半胱氨酸(NAC)抑制。
这些数据提供了令人信服的证据,表明UA是一种有前途的抗白血病细胞系多药耐药的药物,并为白血病提出了一种有前途的治疗方法。