Ashofteh Nooshin, Mahbod Amir Sayed Ali, Bayat Mohammad, Karami Hadi
Department of Molecular Medicine and Biotechnology, Faculty of Medicine, Arak University of Medical Sciences, Arak, Iran.
Department of Parasitology and Mycology, School of Medicine, AJA University of Medical Sciences, Tehran, Iran.
Cell J. 2022 Aug 28;24(8):473-480. doi: 10.22074/cellj.2022.8101.
Objective: Chronic lymphoid leukemia (CLL) is the most common type of leukemia among adults. Increased levels of Mcl-1 and Bcl-xL is linked to resistance to Bcl-2 inhibitors including ABT-199. In this study, we investigated the effect of miRNA-16-1 on apoptosis and sensitivity of the CLL cells to ABT-199.
Materials and Methods: In this experimental study, the Mcl-1 and Bcl-2 expression were measured using qualitative reverse transcription-polymerase chain reaction (qRT-PCR) and western blotting. The effect of treatments on cell survival and growth were explored with MTT assay and Trypan blue assay, respectively. The drug interaction was evaluated using combination index analysis. Apoptosis was assessed by ELISA cell death and caspase-3 activity assays.
Results: MiRNA-16-1 markedly inhibited the expression of Mcl-1 and Bcl-2 in a time dependent manner (P<0.05, relative
to blank control). Pretreatment with miRNA-16-1 synergistically suppressed the cell growth and survival and reduced the half-maximal inhibitory concentration (IC50) value of ABT-199. Moreover, miRNA-16-1 markedly augmented the apoptotic effect of ABT-199 in CLL cells (P<0.05).
Conclusion: Our findings propose that miRNA-16-1 act in concert with ABT-199 to exert synergistic anticancer efficacy against CLL, which is attributed to the inhibition of Bcl-2 and Mcl-1. This may propose a promising strategy for CLL resistant patients.
目的:慢性淋巴细胞白血病(CLL)是成人中最常见的白血病类型。Mcl-1和Bcl-xL水平升高与对包括ABT-199在内的Bcl-2抑制剂耐药有关。在本研究中,我们调查了miRNA-16-1对CLL细胞凋亡及对ABT-199敏感性的影响。
材料与方法:在本实验研究中,采用定性逆转录聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法检测Mcl-1和Bcl-2的表达。分别用MTT法和台盼蓝法探究处理对细胞存活和生长的影响。使用联合指数分析评估药物相互作用。通过ELISA细胞死亡和半胱天冬酶-3活性测定评估细胞凋亡。
结果:MiRNA-16-1以时间依赖性方式显著抑制Mcl-1和Bcl-2的表达(与空白对照相比,P<0.05)。用miRNA-16-1预处理可协同抑制细胞生长和存活,并降低ABT-199的半数最大抑制浓度(IC50)值。此外,miRNA-16-1显著增强了ABT-199对CLL细胞的凋亡作用(P<0.05)。
结论:我们的研究结果表明,miRNA-16-1与ABT-199协同发挥作用,对CLL具有协同抗癌功效,这归因于对Bcl-2和Mcl-1的抑制。这可能为CLL耐药患者提出一种有前景的策略。