Zhou Sijing, Jiang Huihui, Li Min, Wu Peipei, Sun Li, Liu Yi, Zhu Ke, Zhang Binbin, Sun Gengyun, Cao Chao, Wang Ran
Hefei Prevention and Treatment Center for Occupational Diseases, Hefei 230022, China.
Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
Mol Ther Nucleic Acids. 2019 Dec 6;18:275-284. doi: 10.1016/j.omtn.2019.08.026. Epub 2019 Sep 9.
Noncoding RNAs play an important role in the pathogenesis of pulmonary arterial hypertension (PAH). In this study, we investigated the roles of hsa_circ_0016070, miR-942, and CCND1 in PAH. circRNA microarray was used to search circRNAs involved in PAH, whereas real-time PCR and western blot analysis were performed to detect miR-942 and CCND1 expression in different groups. In addition, the effect of miR-942 on CCND1 expression, as well as the effect of hsa_circ_0016070 on the expression of miR-942 and CCND1, was also studied using real-time PCR and western blot analysis. Moreover, MTT assay and flow cytometry were used to detect the effect of hsa _circ_0016070 on cell proliferation and cell cycle. According to the results of circRNA microarray analysis, hsa _circ_0016070 was identified to be associated with the risk of PAH in chronic obstructive pulmonary disease (COPD) patients. The miR-942 level in the COPD(+) PAH(+) group was much lower than that in the COPD(+) PAH(-) group, while the CCND1 level in the COPD(+) PAH(+) group was much higher. CCND1 was identified as a candidate target gene of miR-942, and the luciferase assay showed that the luciferase activity of wild-type CCND1 3' UTR was inhibited by miR-942 mimics. In addition, hsa _circ_0016070 reduced miR-942 expression and enhanced CCND1 expression. Furthermore, hsa _circ_0016070 evidently increased cell viability and decreased the number of cells arrested in the G1/G0 phase. In summary, the results of this study suggested that hsa_circ_0016070 was associated with vascular remodeling in PAH by promoting the proliferation of pulmonary artery smooth muscle cells (PASMCs) via the miR-942/CCND1. Accordingly, has_circ_0016070 might be used as a novel biomarker in the diagnosis and treatment of PAH.
非编码RNA在肺动脉高压(PAH)的发病机制中起重要作用。在本研究中,我们调查了hsa_circ_0016070、miR-942和CCND1在PAH中的作用。利用环状RNA微阵列筛选参与PAH的环状RNA,同时采用实时荧光定量PCR和蛋白质免疫印迹分析检测不同组中miR-942和CCND1的表达。此外,还通过实时荧光定量PCR和蛋白质免疫印迹分析研究了miR-942对CCND1表达的影响,以及hsa_circ_0016070对miR-942和CCND1表达的影响。此外,采用MTT法和流式细胞术检测hsa_circ_0016070对细胞增殖和细胞周期的影响。根据环状RNA微阵列分析结果,确定hsa_circ_0016070与慢性阻塞性肺疾病(COPD)患者PAH的发生风险相关。COPD(+)PAH(+)组中miR-942水平远低于COPD(+)PAH(-)组,而COPD(+)PAH(+)组中CCND1水平远高于COPD(+)PAH(-)组。CCND1被确定为miR-942的候选靶基因,荧光素酶报告基因检测显示miR-942模拟物抑制野生型CCND1 3'UTR的荧光素酶活性。此外,hsa_circ_0016070降低了miR-942的表达并增强了CCND1的表达。此外,hsa_circ_0016070明显增加了细胞活力,并减少了停滞在G1/G0期的细胞数量。总之,本研究结果表明,hsa_circ_0016070通过miR-942/CCND1促进肺动脉平滑肌细胞(PASMCs)增殖,与PAH中的血管重塑相关。因此,hsa_circ_0016070可能作为PAH诊断和治疗的新型生物标志物。