Chu Yanchen, Hu Xiaoli, Wang Guangfeng, Wang Zhijie, Wang Yanjin
Department of Spinal Surgery, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.
Department of Obstetrics and Gynecology, Women and Children's Hospital of Linyi City, Linyi, Shandong 276000, P.R. China.
Oncol Lett. 2019 Jun;17(6):5210-5218. doi: 10.3892/ol.2019.10203. Epub 2019 Apr 1.
Osteosarcoma (OS) is the most common bone tumor in children and young adults, and is an aggressive tumor with poor prognosis. MicroRNAs (miRNAs) are aberrantly expressed in various types of cancer, and contribute to cancer tumorigenesis and progression. In the present study, the potential prognostic value and biological function of miRNA-136 (miR-136) in OS was investigated. Reverse transcription-quantitative polymerase chain reaction analysis was used to evaluate the expression of miR-136 in OS tissues and cell lines. Kaplan-Meier survival analysis and Cox regression analysis were conducted to investigate the prognostic significance of miR-136. Various cell based assays were used to evaluate the effects of miR-136 on the biological behavior of OS cells. A luciferase assay was performed to determine the key miR-136 targets associated with OS. The expression of miR-136 was significantly downregulated in osteosarcoma tissues and cells compared with the normal controls (all P<0.05). Decreased miR-136 expression was significantly associated with Enneking staging (P=0.030) and distant metastasis (P=0.016). Decreased miR-136 expression in patients was associated with shorter overall survival compared with patients with increased expression levels (log-rank test; P<0.05). The expression of miR-136 was indicated as an independent prognostic factor for the patients (hazard ratio=0.496; 95% confidence interval=0.250-0.987; P=0.046). MTT, transwell and Matrigel assays demonstrated that upregulation of miR-136 decreased proliferation, migration and invasion of OS cells. Bioinformatics and luciferase assays demonstrated that migration and invasion enhancer 1 (MIEN1) is a direct target of miR-136. Together, the results suggested that miR-136 functions as a tumor suppressor gene to regulate proliferation, migration and invasion of OS cells. MIEN1 was a potential target of miR-136. Additionally, miR-136 may serve as a prognostic biomarker for OS.
骨肉瘤(OS)是儿童和青年中最常见的骨肿瘤,是一种侵袭性肿瘤,预后较差。微小RNA(miRNA)在各种类型的癌症中表达异常,并促进癌症的发生和发展。在本研究中,研究了miRNA-136(miR-136)在骨肉瘤中的潜在预后价值和生物学功能。采用逆转录-定量聚合酶链反应分析评估miR-136在骨肉瘤组织和细胞系中的表达。进行Kaplan-Meier生存分析和Cox回归分析以研究miR-136的预后意义。使用各种基于细胞的试验来评估miR-136对骨肉瘤细胞生物学行为的影响。进行荧光素酶试验以确定与骨肉瘤相关的关键miR-136靶标。与正常对照相比,骨肉瘤组织和细胞中miR-136的表达明显下调(所有P<0.05)。miR-136表达降低与Enneking分期(P=0.030)和远处转移(P=0.016)显著相关。与表达水平升高的患者相比,患者中miR-136表达降低与总生存期缩短相关(对数秩检验;P<0.05)。miR-136的表达被表明是患者的独立预后因素(风险比=0.496;95%置信区间=0.250-0.987;P=0.046)。MTT、transwell和Matrigel试验表明,miR-136的上调降低了骨肉瘤细胞的增殖、迁移和侵袭。生物信息学和荧光素酶试验表明,迁移和侵袭增强子1(MIEN1)是miR-136的直接靶标。总之,结果表明miR-136作为肿瘤抑制基因发挥作用,调节骨肉瘤细胞的增殖、迁移和侵袭。MIEN1是miR-136的潜在靶标。此外,miR-136可能作为骨肉瘤的预后生物标志物。