期刊文献+

竞争性内源RNA与心血管疾病发病机制的研究进展 被引量:9

Research progress on the pathogenesis of competing endogenous RNA in cardiovascular diseases
原文传递
导出
摘要 微小RNA(miRNA)通过与靶mRNA的3′非编码区(UTR)互补结合,抑制靶mRNA翻译或降低靶mRNA的稳定性,负性调节靶基因的表达;各类转录本,包括mRNA、假基因(pseudogene)、长链非编码RNA(lncRNA)和环状RNA(circRNA)可通过miRNA反应元件(MRE)竞争性结合相同的miRNA,从而调节靶基因的表达,这些RNA转录本称为竞争性内源RNA(ceRNA),这种全新的转录后调控模式称为ceRNA假说。ceRNA不但参与正常细胞的增殖、分化和衰老,在肿瘤、心血管疾病(CVD)等病理过程中亦发挥重要作用。现针对近年来ceRNA在CVD方面的研究进展进行综述。 MicroRNA(miRNA) can reduce the stability of the messenger RNA(mRNA) or inhibit the translation of the messenger RNA by targeting its 3′-untranslated region(UTR), thereby negatively regulate the expression of the target gene.Diverse RNA transcripts including mRNAs; pseudogenes; long non-coding RNAs(LncRNA)and circular RNAs(circRNAs) can competitively combine with the same miRNAs by microRNA response elements(MREs), removing or reducing the inhibition of genes targedted by the miRNAs and regulating the expression of the target genes.These RNA transcripts are called competitive endogenous RNA (ceRNA), and this new post-transcription regulation model is called ceRNA hypothesis.CeRNA not only participates in the proliferation, differentiation and aging of normal cells, but also plays an important role in the pathogenesis of tumor and cardiovascular diseases(CVD). This paper reviewed the studies about ceRNA in cardiovascular diseases in recent years.
作者 朱斌路 姜红堃 Zhu Binlu;Jiang Hongkun(Department of Pediatrics,the First Affiliated Hospital of China Medical University,Shenyang 110001,China(Zhu BL,Jiang IlK)
出处 《中华实用儿科临床杂志》 CSCD 北大核心 2018年第13期1033-1036,共4页 Chinese Journal of Applied Clinical Pediatrics
基金 国家自然科学基金(81300130) 辽宁省高等学校基本科研项目(LFWK201701)
关键词 竞争性内源RNA 心血管疾病 环状RNA 长链非编码RNA 微小RNA Competitive endogenous RNA Cardiovascular diseases Circular RNA Long non-coding RNA miRNA
  • 相关文献

参考文献2

二级参考文献22

  • 1张惠蓉,曹景泰,刘宁朴,贺师鹏.视网膜增殖性疾病玻璃体中表皮生长因子的放射受体定量测定[J].中华眼底病杂志,1996,12(2):91-93. 被引量:12
  • 2李林,李斌,杨安怀,赵婷秀,邢怡桥.人视网膜下膜中ICAM-1及MMP-2的免疫组织化学研究[J].眼科新进展,2005,25(6):519-521. 被引量:3
  • 3黄灵芝,王字玲.CD147的研究进展[J].生物技术通讯,2007,18(3):472-475. 被引量:8
  • 4Yano S, Kondo K, Yamaguchi M, Richmond G, Hutchison M, Wakeling A, et al. Distribution and function of EGFR in human tissue and the effect of EGFR tyrosine kinase inhibition[ J]. An- ticancer Res ,2003,23 (5) :3639-3650.
  • 5Lewis TS, Shapiro PS ,Ahn NG. Signal transduction through MAP kinase cascades[ J]. Adv Cancer Res,1998,74( 1 ) :49-139.
  • 6Bartel DP. MicroRNAs: genomics, biogenesis, mechanism, and function [ J ]. Cell, 2004,116 ( 2 ) : 281-297.
  • 7Griffiths-Jones S, Grocock R J, van Dongen S, Bateman A, En- right A. miRBase: microRNA sequences, targets and gene no- menclature [ J ]. Nucleic Acids Res, 2005,34 ( 1 ) : 140-144.
  • 8Arora A, McKay G J, Simpson DA. Prediction and verification of miRNA expression in human and rat retinasE J]. Invest Ophthal- mol Vis Sci,2007,48 (9) :3962-3957.
  • 9Bravo-Egana V, Rosero S, Molano RD, Pileggi A, Ricordi C, Domlngnez-Bendala J. et al. Quantitative differential expression analysis reveals miR-7 as major islet microRNA [ J ]. Biochem Biophys Res Commun,2008,355 (4) :922-925.
  • 10Cheng AM, Byrom MW, Shelton J, Ford LP. Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis [ J 1. Nucleic Acids Res, 2005,33 (4) : 1290-1297.

共引文献4

同被引文献69

引证文献9

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部