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首页> 外文期刊>FEBS letters. >The lncRNA MALAT1 protects the endothelium against ox-LDL-induced dysfunction via upregulating the expression of the miR-22-3p target genes CXCR2 and AKT
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The lncRNA MALAT1 protects the endothelium against ox-LDL-induced dysfunction via upregulating the expression of the miR-22-3p target genes CXCR2 and AKT

机译:lncRNA MALAT1通过上调miR-22-3p目标基因CXCR2和AKT的表达来保护内皮免受ox-LDL诱导的功能障碍

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摘要

CXCR2 plays a key role in protecting the integrity of the endothelium. Emerging evidence has demonstrated that the long ncRNAs (IncRNA) Human metastasis associated lung adenocarcinoma transcript 1 (MALAT1) participates in the regulation of the pathophysiological processes. However, whether there is crosstalk between CXCR2 and MALAT1 remains unknown. In this study, we demonstrated that MALAT1 was upregulated in patients with unstable angina. MALAT1 silencing significantly downregulated the expression of the miR-22-3p target gene CXCR2 via reversing the effect of the miR-22-3p, resulting in the aggravation of Oxidized low-density lipoprotein (ox-LDL)-induced endothelial injury; this process was associated with the AICT pathway. Thus, MALAT1 protects the endothelium from ox-LDL-induced endothelial dysfunction partly through competing with miR-22-3p for endogenous RNA. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
机译:CXCR2在保护内皮的完整性中起关键作用。新兴证据表明,长ncRNA(IncRNA)人转移相关的肺腺癌转录本1(MALAT1)参与了病理生理过程的调节。但是,CXCR2和MALAT1之间是否存在串扰仍然未知。在这项研究中,我们证明了不稳定型心绞痛患者中MALAT1的表达上调。 MALAT1沉默通过逆转miR-22-3p的作用而显着下调了miR-22-3p目标基因CXCR2的表达,从而加剧了氧化型低密度脂蛋白(ox-LDL)诱导的内皮损伤;这个过程与AICT途径有关。因此,MALAT1部分地通过与miR-22-3p竞争内源RNA来保护内皮免受ox-LDL诱导的内皮功能障碍。 (C)2015年欧洲生物化学学会联合会。由Elsevier B.V.发布。保留所有权利。

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