Li Peng, Wei Lei, Zhu Wenshuai
Department of Spine Orthopaedics, Weifang Traditional Chinese Hospital, Weifang, Shandong 261041, China.
Department of Spinal Surgery, Weifang People's Hospital, Weifang, Shandong 261041, China.
Int J Genomics. 2020 Feb 11;2020:7968407. doi: 10.1155/2020/7968407. eCollection 2020.
Osteosarcoma (OS) is the most frequent bone tumor with high metastasis. This study is aimed at assessing the expression and prognostic significance of microRNA-1826 (miR-1826) in OS patients, as well as its biological function in tumor progression.
Quantitative Real-Time PCR was employed to measure the expression of miR-1826 in OS tissues and cell lines. Kaplan-Meier survival analysis and Cox regression model were used to evaluate the prognostic value of miR-1826. CCK-8 and Transwell assay were conducted to investigate the effect of miR-1826 on OS cell proliferation, migration, and invasion.
miR-1826 expression was downregulated in OS tissues and cell lines and associated with OS patients' clinical stage and distant metastasis. Low levels of miR-1826 were related with shorter survival time and determined as an independent prognostic indicator for the overall survival of OS patients. The overexpression of miR-1826 in OS cells led to inhibited cell proliferation, migration, and invasion.
The decreased expression of miR-1826 predicts a poor prognosis in OS patients, and its overexpression inhibits OS cell proliferation, migration, and invasion. This newly identified miR-1826 provides a novel sight into the pathogenesis of OS and offers a candidate prognostic biomarker and therapeutic target for OS treatment.
骨肉瘤(OS)是最常见的具有高转移率的骨肿瘤。本研究旨在评估微小RNA-1826(miR-1826)在骨肉瘤患者中的表达及预后意义,以及其在肿瘤进展中的生物学功能。
采用定量实时聚合酶链反应(qRT-PCR)检测骨肉瘤组织和细胞系中miR-1826的表达。采用Kaplan-Meier生存分析和Cox回归模型评估miR-1826的预后价值。进行CCK-8和Transwell实验以研究miR-1826对骨肉瘤细胞增殖、迁移和侵袭的影响。
miR-1826在骨肉瘤组织和细胞系中的表达下调,且与骨肉瘤患者的临床分期和远处转移相关。低水平的miR-1826与较短的生存时间相关,并被确定为骨肉瘤患者总生存的独立预后指标。miR-1826在骨肉瘤细胞中的过表达导致细胞增殖、迁移和侵袭受到抑制。
miR-1826表达降低预示骨肉瘤患者预后不良,其过表达抑制骨肉瘤细胞增殖、迁移和侵袭。新发现的miR-1826为骨肉瘤的发病机制提供了新的视角,并为骨肉瘤治疗提供了一个候选的预后生物标志物和治疗靶点。