Micro-RNA-140-3p Acts as a Tumor Suppressor Gene in Acute Promyelocytic Leukemia by Targeting Hepatocyte Growth Factor.

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
RuiQi Lei, Xin Liu, YiTing Wu, JingYu Song, XiaoLi Lv, Jie Liu, Dan Guo, ShengJin Fan, HuiBo Li
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引用次数: 0

Abstract

MicroRNAs (miRNAs) are noncoding RNAs that regulate the expression of target genes after transcription, and play important roles in the differentiation of hematopoietic stem cells. Many miRNAs are related to the occurrence of acute promyelocytic leukemia (APL) and play roles in the treatment response. Recently, we demonstrated that several miRNAs are differentially expressed in patients with relapsed and newly diagnosed APL; for example, miR-140-3p is significantly downregulated in patients with relapsed APL. In this study, via a dual luciferase assay, we verified that one of the direct target genes of miR-140-3p is hepatocyte growth factor (HGF). After different lentiviruses were transfected into NB4 cells, and flow cytometry and proliferation assays confirmed that low expression of miR-140-3p inhibited the differentiation and apoptosis of NB4 cells and induced proliferation by promoting cell cycle progression. In summary, our findings suggest that hepatocyte growth factor is a target gene of miR-140-3p. Moreover, upregulation of miR-140-3p expression in APL cells inhibits cell proliferation, arrests cell cycle progression, and promotes apoptosis and cell differentiation. Monitoring the levels of miR-140-3p and HGF may predict the risk of disease recurrence, and interfering with the miR-140-3p / HGF pathway may have therapeutic potential for treating recurrent APL.

靶向肝细胞生长因子的微rna -140-3p在急性早幼粒细胞白血病中作为肿瘤抑制基因
MicroRNAs (miRNAs)是一种经转录后调控靶基因表达的非编码rna,在造血干细胞分化过程中发挥重要作用。许多mirna与急性早幼粒细胞白血病(APL)的发生有关,并在治疗反应中发挥作用。最近,我们证明了几种mirna在复发和新诊断的APL患者中存在差异表达;例如,miR-140-3p在APL复发患者中显著下调。在本研究中,通过双荧光素酶测定,我们证实了miR-140-3p的直接靶基因之一是肝细胞生长因子(HGF)。将不同慢病毒转染NB4细胞后,流式细胞术和增殖实验证实,miR-140-3p低表达抑制NB4细胞的分化和凋亡,并通过促进细胞周期进展诱导增殖。综上所述,我们的研究结果表明肝细胞生长因子是miR-140-3p的靶基因。此外,APL细胞中miR-140-3p表达上调可抑制细胞增殖,阻滞细胞周期进程,促进细胞凋亡和细胞分化。监测miR-140-3p和HGF的水平可以预测疾病复发的风险,干扰miR-140-3p / HGF通路可能具有治疗复发性APL的治疗潜力。
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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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