首页> 美国卫生研究院文献>Molecular Medicine Reports >Overexpression of miR-199b-5p inhibits Ewings sarcoma cell lines by targeting CCNL1
【2h】

Overexpression of miR-199b-5p inhibits Ewings sarcoma cell lines by targeting CCNL1

机译:miR-199b-5p的过度表达通过靶向CCNL1抑制Ewing的肉瘤细胞系

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

MicroRNAs (miRNAs) are known to regulate the expression of a variety of genes, which are important in the development of several types of tumor, including Ewing's sarcoma (ES), at the post-transcriptional level. Although previous studies have identified that the expression of miRNA-199b-5p was downregulated in various types of tumor, the expression levels of miR-199b-5p in ES cells remain to be elucidated. The mechanism underlying ES via the miRNA pathway remains to be elucidated. The present study demonstrated that miR-199b-5p was an important regulator in ES cells and its expression was downregulated in ES originated A673/TC252 cells. The ES cell lines, A673 and TC252, were transfected with an miR-199b-5p mimic to overexpress the levels of this miRNA. This forced expression of miR-199b-5p suppressed the cell proliferation and invasion, arrested cell cycle progression, and promoted cell apoptosis. Furthermore, CCNL1 was identified by bioinformatic software as a potential target gene of miR-199b-5p. Following this, the present study identified CCNL1 as a direct target of miR-199b-5p in ES cells. Taken together, the present study established a functional link between ES, miR-199b-5p and CCNL1, and suggested that miR-199b-5p acts as a tumor suppressor and may be of diagnostic and therapeutic importance for human ES.
机译:已知MicroRNA(miRNA)在转录后水平上调节多种基因的表达,这在包括尤因氏肉瘤(ES)在内的几种类型肿瘤的发展中起着重要作用。尽管以前的研究已经确定了在各种类型的肿瘤中miRNA-199b-5p的表达均被下调,但ES细胞中miR-199b-5p的表达水平仍有待阐明。 ES通过miRNA途径的潜在机制尚待阐明。本研究表明,miR-199b-5p是ES细胞中的重要调控因子,其表达在ES起源的A673 / TC252细胞中被下调。用miR-199b-5p模拟物转染ES细胞系A673和TC252,以过度表达该miRNA的水平。 miR-199b-5p的这种强制表达抑制了细胞增殖和侵袭,阻止了细胞周期进程,并促进了细胞凋亡。此外,通过生物信息学软件将CCNL1鉴定为miR-199b-5p的潜在靶基因。此后,本研究确定CCNL1是ES细胞中miR-199b-5p的直接靶标。综上所述,本研究建立了ES,miR-199b-5p和CCNL1之间的功能联系,并建议miR-199b-5p充当肿瘤抑制因子,可能对人类ES具有诊断和治疗意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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