...
首页> 外文期刊>Pathology Research and Practice >Circular RNA circ_0102049 promotes cell progression as ceRNA to target MDM2 via sponging miR-1304-5p in osteosarcoma
【24h】

Circular RNA circ_0102049 promotes cell progression as ceRNA to target MDM2 via sponging miR-1304-5p in osteosarcoma

机译:循环RNA QIC_0102049通过在骨肉瘤中通过冲水MIR-1304-5P促进细胞进展,以靶向MDM2

获取原文
获取原文并翻译 | 示例

摘要

Osteosarcoma (OS) is known as a tumor that derives from skeletal system with increasing incidence worldwide. This study aimed to explore the effect of a circular RNA (circRNA), circ_0102049, on OS and reveal its potential molecular mechanism. In this work, the expression of circ_0102049 was detected by quantitative real time polymerase chain reaction (qRT-RCR) in both OS specimens and cell lines. The relationship between circ_0102049 level and patients’ overall survival was evaluated by Kaplan-Meier curves and Cox regression analysis. Cell proliferation, apoptosis, migration and invasion of U2OS and MG63 cells were measured by cell counting kit-8 (CCK-8), flow cytometry, wound healing and transwell experiments, respectively. In addition, subcellular fractionation, bioinformatics analysis and dual-luciferase reporter assay were utilized to reveal the mechanism of circ_0102049 in OS. Circ_0102049 was overexpressed in both OS specimens and cells. Moreover, the level of circ_0102049 in OS patients was markedly correlated with larger tumor size, pulmonary metastasis and poor prognosis. Circ_0102049 remarkably accelerated cell proliferation, migration and invasion but attenuated cell apoptosis in OS cells analyzed by gain/loss of function experiments. What’s more, we identified that circ_0102049 functions as a competing endogenous RNA (ceRNA) to competitively sponge miR-1304-5p to upregulate MDM2 expression at posttranscriptional level, thus mediating the cellular behaviors of OS cells. Collectively, our study provides an innovatively regulatory mechanism of circ_0102049 in OS and points out a new way for OS treatment.
机译:骨肉瘤(OS)被称为肿瘤,其源于骨骼系统,在全世界越来越多的入学率。本研究旨在探讨圆形RNA(CircrNA),Circ_0102049,OS和揭示其潜在分子机制的影响。在这项工作中,通过两种OS样本和细胞系中的定量实时聚合酶链反应(QRT-RCR)检测CIRC_0102049的表达。 Kaplan-Meier曲线和Cox回归分析评估了Circ_0102049水平与患者整体生存之间的关系。通过细胞计数试剂盒-8(CCK-8),流式细胞术,伤口愈合和Transwell实验分别测量U2OS和Mg63细胞的细胞增殖,凋亡,迁移和侵袭。此外,利用亚细胞分级,生物信息学分析和双荧光素酶报告结果来揭示OS中循环_0102049的机制。 Circ_0102049在OS样本和细胞中过表达。此外,OS患者中的CIRC_0102049水平与较大的肿瘤大小,肺转移和预后差异显着相关。 CIRC_0102049通过增益/丧失功能实验分析的OS细胞中显着加速的细胞增殖,迁移和侵袭,但减毒细胞凋亡。更重要的是,我们确定Circ_0102049作为竞争内源性RNA(Cerna),以竞争激发miR-1304-5p以上调在后术语水平时上调MDM2表达,从而介导OS细胞的细胞行为。统称,我们的研究提供了一种在OS中的CIRC_0102049的创新调节机制,并指出了一种新的OS治疗方式。

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