Fasihi-Ramandi Mahdi, Moridnia Abbas, Najafi Ali, Sharifi Mohammadreza
1Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
2Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Science, Isfahan, 81744-176 Iran.
Indian J Hematol Blood Transfus. 2018 Jan;34(1):70-77. doi: 10.1007/s12288-017-0809-9. Epub 2017 Mar 29.
MicroRNAs (miRNAs) are short and single strand non-coding RNAs that involved in post-transcriptional regulation of gene expression. Dysregulation of miRNA expression is important event in the many of malignant diseases. Up-regulation of Let-7a-5p expression in acute myeloid leukemia in human in previous studies was reported. In this study blockage of Let-7a-5p in human acute promyelocytic leukemia cell line (HL60) was done by using locked nucleic acid (LNA) method and subsequently expression of Let-7a-5p, cell proliferation, apoptosis, necrosis, and expression was measured. At three time points 24, 48 and 72 h after LNA anti- Let-7a-5p transfection, assessment of Let-7a-5p expression by qRT real-time PCR was completed. The MTT assay and annexin/PI staining have been performed. Also, expression at different time points after LNA anti-Let-7a-5p transfection in HL60 cell line was measured. The results at three-time points after LNA transfection were represented that Let-7a-5p expression was lower in the LNA-anti-Let-7a group compared to the control groups. The cell viability significantly was different between LNA-anti-Let-7a group and control groups. Increasing apoptotic ratio was associated with Let-7a-5p blockage in the LNA-anti-Let-7a group compared with control groups. Also, the necrotic ratio was higher in the LNA-anti-Let-7a group rather than the other groups. Western blotting revealed that CASP3 expression associated with Let-7a-5p inhibition. Our results displayed that blockage of Let-7a-5p can reduced cell viability mainly due to the induction of apoptosis and up-regulation in HL60 cells. These results can be useful in translational medicine for research of antisense therapy in leukemia.
微小RNA(miRNA)是短链单链非编码RNA,参与基因表达的转录后调控。miRNA表达失调是许多恶性疾病中的重要事件。先前的研究报道了人类急性髓系白血病中Let-7a-5p表达上调。在本研究中,采用锁核酸(LNA)方法阻断人类急性早幼粒细胞白血病细胞系(HL60)中的Let-7a-5p,随后检测Let-7a-5p的表达、细胞增殖、凋亡、坏死及相关表达。在LNA抗Let-7a-5p转染后的24、48和72小时三个时间点,通过qRT实时PCR完成对Let-7a-5p表达的评估。进行了MTT试验和膜联蛋白/PI染色。此外,还检测了LNA抗Let-7a-5p转染后HL60细胞系不同时间点的相关表达。LNA转染后三个时间点的结果表明,与对照组相比,LNA抗Let-7a组中Let-7a-5p表达较低。LNA抗Let-7a组与对照组之间的细胞活力存在显著差异。与对照组相比,LNA抗Let-7a组中凋亡率增加与Let-7a-5p阻断有关。此外,LNA抗Let-7a组的坏死率高于其他组。蛋白质印迹法显示CASP3表达与Let-7a-5p抑制有关。我们的结果表明,阻断Let-7a-5p可降低细胞活力,主要是由于HL60细胞中凋亡的诱导和相关上调。这些结果在白血病反义治疗的转化医学研究中可能有用。