Department of Clinical Laboratory, Jiading District Central Hospital Affiliated to Shanghai Health Medical College, Shanghai, China.
Bioengineered. 2021 Dec;12(1):2906-2914. doi: 10.1080/21655979.2021.1915727.
MicroRNAs (miRNAs) play a very important role in the development of acute myeloid leukemia (AML). This study focuses on the effects of miR-9 on the regulation of AML cells and their related signaling pathways. We found that the expression of miR-9 was significantly decreased in four AML cell lines (THP-1, HL-60, TF-1 and KG-1) compared with the human normal bone marrow cells (HS-5). Moreover, miR-9 overexpression inhibited HL-60 cell proliferation ability, and promoted apoptosis. However, interfering with miR-9 expression promoted the proliferation of HL-6 cells and inhibited apoptosis. Western blotting results subsequently showed that overexpression of miR-9 could elevate the expression of MAT1, LATS1, and LATS2 in HL-60 cells, and inhibit the expression of YAP, while the interference with miR-9 had the opposite result. Taken together, miR-9 may act as a tumor suppressor by activating the Hippo/YAP signaling pathway of AML cells, which in this way supply ideas for the clinical remedy of AML patients.
微小 RNA(miRNAs)在急性髓系白血病(AML)的发展中起着非常重要的作用。本研究专注于 miR-9 对 AML 细胞及其相关信号通路的调节作用。我们发现,与正常人骨髓细胞(HS-5)相比,在四种 AML 细胞系(THP-1、HL-60、TF-1 和 KG-1)中 miR-9 的表达明显降低。此外,miR-9 的过表达抑制 HL-60 细胞的增殖能力,并促进细胞凋亡。然而,干扰 miR-9 的表达促进了 HL-6 细胞的增殖并抑制了细胞凋亡。Western blot 结果随后表明,miR-9 的过表达可以上调 HL-60 细胞中 MAT1、LATS1 和 LATS2 的表达,并抑制 YAP 的表达,而干扰 miR-9 的表达则产生相反的结果。综上所述,miR-9 可能通过激活 AML 细胞的 Hippo/YAP 信号通路发挥肿瘤抑制作用,这为 AML 患者的临床治疗提供了思路。