Hosseini Maryam Sadat, Mohammadi Mohammad Hossein, Vahabpour Roudsari Rouhollah, Jafari Leila, Mashati Pargol, Gharehbaghian Ahmad
Department of Laboratory Hematology and Blood Bank, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
HSCT Research Center, Department of Laboratory Hematology and Blood Bank, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Iran J Pharm Res. 2019 Fall;18(Suppl1):132-145. doi: 10.22037/ijpr.2020.112692.13898.
T-cell acute lymphoblastic leukemia is an aggressive hematologic malignancy which is usually associated with unfavorable prognosis particularly in patients with refractory/relapsed disease. Therefore, development of novel therapeutic strategies is highly required for improving the outcome of these patients. Although there are several studies evaluating the efficacy of proteasome inhibitors on acute lymphoblastic leukemia of B-cell lineage, the data are still limited regarding T-cell acute lymphoblastic leukemia. Here, we tried to investigate the effects of the proteasome inhibition by carfilzomib on the induction of apoptosis and autophagy in Molt4 cells. The effect of carfilzomib in combination with dexamethasone in Molt4, as a glucocorticoid-resistant T-cell acute lymphoblastic leukemia cell line, was also assessed. Our data showed that carfilzomib can induce both apoptosis and autophagy in Molt4 cells. Furthermore, we found that carfilzomib is a potent inducer of reactive oxygen species production and also induces G2/M phase cell cycle arrest in Molt4 cells. Concomitant treatment with carfilzomib and dexamethasone demonstrated that carfilzomib can synergistically enhance the cytotoxic effect of dexamethasone on Molt4 cells. Furthermore, co-treatment of the cells with carfilzomib and dexamethasone increased the induction of autophagy as compared with each drug alone. In conclusion, our results are suggestive of the effectiveness of carfilzomib on Molt4 cells as a model of GC-resistant T-cell acute lymphoblastic leukemia.
T细胞急性淋巴细胞白血病是一种侵袭性血液系统恶性肿瘤,通常预后不佳,尤其是难治性/复发性疾病患者。因此,迫切需要开发新的治疗策略来改善这些患者的治疗效果。尽管有多项研究评估蛋白酶体抑制剂对B细胞系急性淋巴细胞白血病的疗效,但关于T细胞急性淋巴细胞白血病的数据仍然有限。在此,我们试图研究卡非佐米抑制蛋白酶体对Molt4细胞凋亡和自噬诱导的影响。还评估了卡非佐米与地塞米松联合对Molt4细胞(一种糖皮质激素耐药的T细胞急性淋巴细胞白血病细胞系)的作用。我们的数据表明,卡非佐米可诱导Molt4细胞凋亡和自噬。此外,我们发现卡非佐米是活性氧产生的有效诱导剂,还可诱导Molt4细胞G2/M期细胞周期阻滞。卡非佐米与地塞米松联合治疗表明,卡非佐米可协同增强地塞米松对Molt4细胞的细胞毒性作用。此外,与单独使用每种药物相比,卡非佐米和地塞米松联合处理细胞可增加自噬诱导。总之,我们的结果提示卡非佐米对作为糖皮质激素耐药T细胞急性淋巴细胞白血病模型的Molt4细胞有效。