Deng Haiqing, Xie Changping, Ye Yi, Du Zhenglong
Department of Cardiothoracic Surgery, The Second People's Hospital of Qinzhou, Qinzhou, Guangxi 535000, P.R. China.
Oncol Lett. 2020 Jan;19(1):623-630. doi: 10.3892/ol.2019.11154. Epub 2019 Nov 28.
MicroRNAs (miRNAs) are vital regulators of non-small cell lung cancer (NSCLC) development and tumorigenesis. The aim of the present study was to explore the role of miRNA (miR)-1296 expression in NSCLC. The expression of miR-1296 was detected by reverse transcription-quantitative PCR in NSCLC tissues and matched normal tissues. The association of miR-1296 expression with clinicopathological factors of NSCLC patients was evaluated by the χ test. Prognostic value of miR-1296 expression levels in patients with NSCLC was assessed using the Kaplan-Meier method and a Cox proportional hazards model; Cell Counting Kit-8, Transwell migration and western blot assays were used to detect the association between miR-1296 and cell proliferation, invasion and Wnt signaling in NSCLC, respectively. The results of the present study demonstrated that miR-1296 expression was significantly downregulated in NSCLC tissues and cells compared to corresponding controls. Lower miR-1296 expression exhibited a significant association with lymph node metastasis and tumor-node-metastasis stage of patients with NSCLC. In addition, the survival analysis demonstrated that low miR-1296 expression predicted a poorer prognosis compared to high miR-1296 expression. Multivariate Cox analysis also demonstrated that reduced miR-1296 expression was an independent risk factor of NSCLC prognosis. Additionally, miR-1296 inhibited cell proliferation, invasion and Wnt signaling in NSCLC. Thus, the results of the present study indicated that miR-1296 expression may be a potential biomarker of NSCLC prognosis and potential target for NSCLC treatment.
微小RNA(miRNA)是非小细胞肺癌(NSCLC)发生发展和肿瘤形成的重要调节因子。本研究旨在探讨miRNA(miR)-1296表达在NSCLC中的作用。采用逆转录定量PCR检测NSCLC组织及配对正常组织中miR-1296的表达。通过χ检验评估miR-1296表达与NSCLC患者临床病理因素的相关性。采用Kaplan-Meier法和Cox比例风险模型评估miR-1296表达水平对NSCLC患者的预后价值;分别采用细胞计数试剂盒-8、Transwell迁移实验和蛋白质印迹法检测miR-1296与NSCLC细胞增殖、侵袭及Wnt信号通路之间的关系。本研究结果表明,与相应对照相比,NSCLC组织和细胞中miR-1296表达显著下调。较低的miR-1296表达与NSCLC患者的淋巴结转移及肿瘤-淋巴结-转移分期显著相关。此外,生存分析表明,与高miR-1296表达相比,低miR-1296表达预示预后较差。多因素Cox分析还表明,miR-1296表达降低是NSCLC预后的独立危险因素。此外,miR-1296抑制NSCLC细胞的增殖、侵袭及Wnt信号通路。因此,本研究结果表明,miR-1296表达可能是NSCLC预后的潜在生物标志物及NSCLC治疗的潜在靶点。