Chen Zi, Zhao Guohui, Zhang Yunkun, Ma Yong, Ding Yin, Xu Nanwei
Department of Orthopaedics, Changzhou No.2 People's Hospital Affiliated to Nanjing Medical University, 68th Gehu Middle Rd, Wujing District, Changzhou 213000, Jiangsu, China.
J BUON. 2018 Nov-Dec;23(6):1816-1824.
MicroRNAs (miRs) are endogenous, noncoding small RNAs that play a key role in regulating biological and pathological processes. The oncogenic properties of miR-199b-5p have been demonstrated in previous studies but the effect of miR-199b-5p on osteosarcoma (OS) has not yet been clarified. This study aimed to investigate the effect of miR-199b-5p on OS and the relationship between this miR and the pathological parameters and prognosis of OS.
MiR-199b-5p expression in 57 pairs of OS tissues, corresponding adjacent normal tissues and OS cells was measured by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR).The relationship between miR-199b-5p and the pathological features and prognosis of OS patients was examined. We constructed small interfering (si) RNA to knock down miR-199b-5p expression in OS cell lines MG63 and U2OS. Cell Counting Kit-8 (CCK-8), cell cloning assay and Transwell cell migration and invasion assay were applied for investigating the biological function of miR-199b-5p, respectively. Finally, western blot was used for exploring its underlying mechanism.
MiR-199b-5p expression in OS was significantly higher than that of normal tissues. Compared to patients w\sith low expression of miR-199b-5p, patients with high expression level tended to be with younger age, higher incidence of distant metastases and lower overall survival. Compared with interference sequence negative control (si-NC) group, the abilities of proliferation, invasion and metastasis of cells transfected with si-miR-199b-5p were significantly decreased. Western blot analysis indicated that expressions of key proteins related to epithelial to mesenchymal transition (EMT) signaling pathway, including N-cadherin, Vimentin, β-catenin and matrix metalloproteinase-9 (MMP9), were significantly decreased after transfection with si-miR-199b-5p. Furthermore, we found that miR-199b-5p promoted the progression of OS mainly through regulating HER2.
Upregulated miR-199b-5p is significantly related with stage, distant metastasis and poor prognosis of OS. This MiR may promote progression of OS through regulating HER2.
微小RNA(miR)是内源性非编码小RNA,在调节生物和病理过程中起关键作用。先前的研究已证实miR-199b-5p具有致癌特性,但miR-199b-5p对骨肉瘤(OS)的影响尚未阐明。本研究旨在探讨miR-199b-5p对OS的影响以及该miR与OS病理参数和预后的关系。
采用定量逆转录聚合酶链反应(qRT-PCR)检测57对OS组织、相应的癌旁正常组织及OS细胞中miR-199b-5p的表达。检测miR-199b-5p与OS患者病理特征及预后的关系。构建小干扰(si)RNA以敲低OS细胞系MG63和U2OS中miR-199b-5p的表达。分别应用细胞计数试剂盒-8(CCK-8)、细胞克隆实验及Transwell细胞迁移和侵袭实验研究miR-199b-5p的生物学功能。最后,采用蛋白质印迹法探讨其潜在机制。
OS中miR-199b-5p的表达明显高于正常组织。与miR-199b-5p低表达患者相比,高表达水平患者往往年龄较小、远处转移发生率较高且总生存期较短。与干扰序列阴性对照(si-NC)组相比,转染si-miR-199b-5p的细胞增殖、侵袭和转移能力明显降低。蛋白质印迹分析表明,转染si-miR-199b-5p后,与上皮-间质转化(EMT)信号通路相关的关键蛋白,包括N-钙黏蛋白、波形蛋白、β-连环蛋白和基质金属蛋白酶-9(MMP9)的表达明显降低。此外,我们发现miR-199b-5p主要通过调节HER2促进OS的进展。
miR-199b-5p上调与OS的分期、远处转移及不良预后显著相关。该miR可能通过调节HER2促进OS的进展。