首页> 外文期刊>International Journal of Genomics >Downregulation of miR-1826 Indicates a Poor Prognosis for Osteosarcoma Patients and Regulates Tumor Cell Proliferation, Migration, and Invasion
【24h】

Downregulation of miR-1826 Indicates a Poor Prognosis for Osteosarcoma Patients and Regulates Tumor Cell Proliferation, Migration, and Invasion

机译:miR-1826的下调表明骨肉瘤患者的预后差,并调节肿瘤细胞增殖,迁移和入侵

获取原文

摘要

Background. 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. Methods. 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. Results. 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. Conclusion. 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.
机译:背景。骨质肉瘤(OS)是最常见的骨肿瘤,具有高转移。本研究旨在评估MicroRNA-1826(miR-1826)在OS患者中的表达和预后意义,以及其在肿瘤进展中的生物学功能。方法。使用定量实时PCR测量MIR-1826在OS组织和细胞系中的表达。 Kaplan-Meier生存分析和Cox回归模型用于评估miR-1826的预后价值。进行CCK-8和Transwell测定以研究miR-1826对OS细胞增殖,迁移和侵袭的影响。结果。 miR-1826表达在OS组织和细胞系中下调,与OS患者的临床阶段和远处转移相关。低水平的miR-1826与较短的存活时间有关,并确定为OS患者的整体存活的独立预后指标。 MIR-1826在OS细胞中的过表达导致抑制细胞增殖,迁移和侵袭。结论。 miR-1826的表达减少预测OS患者的预后差,其过表达抑制OS细胞增殖,迁移和侵袭。该新发现的miR-1826提供了一种新的景点,进入OS的发病机制,并提供候选预后生物标志物和OS治疗的治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号