Hu Ning, Chen Li, Li Qianyu, Zhao Hongmian
Department of Hematology, Huaihe Hospital of Henan University No. 115 Ximen Street Kaifeng 475000 Henan China
RSC Adv. 2019 Apr 2;9(18):10352-10359. doi: 10.1039/c9ra00142e. eCollection 2019 Mar 28.
LncRNAs have been shown to be involved in the biological and pathological processes of acute myeloid leukemia (AML). Hox antisense intergenic RNA myeloid 1 (HOTAIRM1) was reported to be highly expressed in AML. However, the detailed role and molecular mechanism of HOTAIRM1 in AML pathogenesis remain undefined. In the present study, HOTAIRM1 and miR-148b expressions in AML patients and healthy controls were detected by qRT-PCR. Cell proliferation and apoptosis were evaluated by CCK-8 and flow cytometry assays, respectively. The regulatory interaction between HOTAIRM1 and miR-148b was explored by bioinformatics analysis using starBase v3.0 software and The Cancer Genome Atlas (TCGA) AML dataset. We found that the miR-148/miR-152 family members including miR-148a, miR-148b, and miR-152 were predicted to be potential targets of HOTAIRM1. HOTAIRM1 expression was negatively correlated with miR-148b expression but had no correlation with miR-148a/miR-152 expressions in AML samples from the TCGA dataset. HOTAIRM1 expression was higher while miR-148b expression was lower in AML patients than in healthy controls. A negative correlation between HOTAIRM1 and miR-148b in AML patients was observed. HOTAIRM1 silencing and miR-148b overexpression both suppressed cell proliferation and induced apoptosis in AML cells. miR-148b was identified as a target of HOTAIRM1 in AML cells. Moreover, HOTAIRM1 knockdown inhibited proliferation and induced apoptosis in AML cells by negatively regulating miR-148b. In summary, HOTAIRM1 was involved in the progression of AML through targeting miR-148b, shedding light on the biological function and molecular mechanism of HOTAIRM1 in AML.
长链非编码RNA(lncRNAs)已被证明参与急性髓系白血病(AML)的生物学和病理过程。据报道,Hox反义基因间RNA髓系1(HOTAIRM1)在AML中高表达。然而,HOTAIRM1在AML发病机制中的具体作用和分子机制仍不明确。在本研究中,通过qRT-PCR检测了AML患者和健康对照中HOTAIRM1和miR-148b的表达。分别通过CCK-8和流式细胞术检测细胞增殖和凋亡。使用starBase v3.0软件和癌症基因组图谱(TCGA)AML数据集,通过生物信息学分析探索HOTAIRM1与miR-148b之间的调控相互作用。我们发现,包括miR-148a、miR-148b和miR-152在内的miR-148/miR-152家族成员被预测为HOTAIRM1的潜在靶点。在TCGA数据集中的AML样本中,HOTAIRM1表达与miR-148b表达呈负相关,但与miR-148a/miR-152表达无相关性。AML患者中HOTAIRM1表达高于健康对照,而miR-148b表达低于健康对照。观察到AML患者中HOTAIRM1与miR-