Blood Group Reference Laboratory, Shandong Blood Center, Jinan, Shandong 250014, P.R. China.
Int J Mol Med. 2018 Dec;42(6):3364-3370. doi: 10.3892/ijmm.2018.3925. Epub 2018 Oct 10.
microRNA (miRNA)‑26a‑loaded liposomes were prepared in the present study for effective treatment of leukemia. The results demonstrated that miRNA‑26a reduced the viability of chronic lymphocytic leukemia (CLL) cells in a concentration‑dependent manner. Cells treated with miRNA‑26a‑loaded liposomes exhibited increased rates of apoptosis, as determined by flow cytometry and Hoechst 33342 staining. Western blot analysis revealed an increased apoptotic effect of miRNA‑26a‑loaded liposomes compared with control. Treatment with these liposomes resulted in significant downregulation of the expression of the miRNA‑26a target genes, myeloid cell leukemia 1 and cyclin‑dependent kinase 6. Taken together, the results of the present study indicate that miRNA‑26a exerts apoptosis‑inducing and anticancer effects on leukemia cells, suggesting therapeutic potential. This approach may be possible to extrapolate to other neoplasms, including lymphomas and acute myeloid leukemia.
本研究制备了负载 microRNA(miRNA)-26a 的脂质体,用于有效治疗白血病。结果表明,miRNA-26a 以浓度依赖的方式降低慢性淋巴细胞白血病(CLL)细胞的活力。通过流式细胞术和 Hoechst 33342 染色测定,用负载 miRNA-26a 的脂质体处理的细胞显示出更高的凋亡率。Western blot 分析显示,负载 miRNA-26a 的脂质体的凋亡作用明显高于对照组。用这些脂质体处理导致 miRNA-26a 靶基因髓样细胞白血病 1 和细胞周期蛋白依赖性激酶 6 的表达显著下调。综上所述,本研究结果表明,miRNA-26a 对白血病细胞具有诱导凋亡和抗癌作用,提示其具有治疗潜力。这种方法可能可以推广到其他肿瘤,包括淋巴瘤和急性髓细胞性白血病。