...
首页> 外文期刊>Cancer Cell International >Inhibition of breast cancer cell proliferation and tumorigenesis by long non-coding RNA RPPH1 down-regulation of miR-122 expression
【24h】

Inhibition of breast cancer cell proliferation and tumorigenesis by long non-coding RNA RPPH1 down-regulation of miR-122 expression

机译:长期非编码RNA RPPH1下调miR-122表达抑制乳腺癌细胞的增殖和肿瘤发生

获取原文
           

摘要

Recent studies showed that long non-coding RNA (lncRNA) plays an important role in many life activities. RPPH1 is one of the lncRNA genes that are expressed differently between breast cancer and normal tissues by the lncRNA gene chip. Our study was conducted to examine the regulation of lncRNA RPPH1 in breast cancer. Two cell lines, MCF-7 and MDA-MB-231, were selected to be the research objects in this study; RPPH1 overexpression and knockdown models were established by transforming vectors. Real-time polymerase chain reaction, MTT assay, clone formation and cell flow cytometer assay were used to test the function of RPPH1. Dual-luciferase assay was used to detect a target relationship between RPPH1 and miR-122. RPPH1 overexpression promoted cell cycle and proliferation and increased colony formation. In the RPPH1 overexpression model, there was a target relationship between RPPH1 and miR-122, and some of the downstream genes of miR-122, including ADAM10, PKM2, NOD2 and IGF1R, were increased. Moreover, we found that lentivirus-mediated interference of lncRNA RPPH1 inhibited tumour growth in nude mice. Breast cancer progression can be promoted by directly targeting miR-122 through lncRNA RPPH1. This study provided evidence that can serve as the molecular basis for improving treatment options for patients.
机译:最近的研究表明,长的非编码RNA(lncRNA)在许多生命活动中起着重要作用。 RPPH1是lncRNA基因之一,通过lncRNA基因芯片在乳腺癌和正常组织之间表达差异。我们的研究旨在检查lncRNA RPPH1在乳腺癌中的调控。选择两种细胞系MCF-7和MDA-MB-231作为本研究的研究对象。通过转化载体建立了RPPH1过表达和敲低模型。实时聚合酶链反应,MTT测定,克隆形成和细胞流式细胞仪测定被用来测试RPPH1的功能。使用双重荧光素酶测定法检测RPPH1和miR-122之间的靶标关系。 RPPH1过表达促进细胞周期和增殖并增加集落形成。在RPPH1过表达模型中,RPPH1和miR-122之间存在靶标关系,miR-122的某些下游基因(包括ADAM10,PKM2,NOD2和IGF1R)增加了。此外,我们发现慢病毒介导的lncRNA RPPH1干扰抑制了裸鼠中的肿瘤生长。可以通过lncRNA RPPH1直接靶向miR-122来促进乳腺癌的进展。这项研究提供了证据,可以作为改善患者治疗选择的分子基础。

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