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首页> 外文期刊>Biochemical and Biophysical Research Communications >The expression profiles of circRNAs in lung tissues from rats with lipopolysaccharide-induced acute respiratory distress syndrome: A microarray study
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The expression profiles of circRNAs in lung tissues from rats with lipopolysaccharide-induced acute respiratory distress syndrome: A microarray study

机译:脂多糖诱导急性呼吸窘迫综合征大鼠肺组织中Circrnas的表达谱:微阵列研究

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Abstract The development of circular RNA (circRNA) microarray has facilitated the study of the role of circRNAs in regulating gene expression through a circRNA-miRNA-mRNA network. In our study, microarray was performed to detect the expression profiles of circRNAs during lipopolysaccharide (LPS)-induced acute respiratory distress syndrome (ARDS). Twenty rats were randomly divided into 2 groups, the control group and the LPS group, 10 rats in each group. Three rats each from both groups were randomly selected. Using circRNA microarray data, we compared the circRNA expression profiles in lung tissues between these 6 rats. The most differentially expressed circRNA species from these profiles were validated and optimized as ARDS biomarkers and potential therapeutic targets. Overall, 395 and 562 circRNAs were significantly up- and down-regulated in LPS group vs. control group, respectively. Six up-regulated and 4 down-regulated circRNAs from the top 10 candidates were eventually selected to be validated. Among them, only 4 up-regulated circRNAs (mmu_circRNA_19423, rno_circRNA_010489, rno_circRNA_011426, mmu_circRNA_30664) and 1 down-regulated circRNA (rno_circRNA_005564) exhibited significant validation. The 5 highest ranking target miRNAs of these 5 validated circRNAs were predicted according to the miRNA support vector regression method. This is the first study to investigate circRNA expression profile and a large number of aberrantly expressed circRNAs were revealed during ARDS. The significantly over- or under-expressed circRNA may represent a novel biomarker and be developed as a novel therapeutic target for the clinical management of ARDS. The results are preliminary and need to be confirmed in further well-designed studies with larger sample size.
机译:摘要圆形RNA(CircrNA)微阵列的发展促进了Circrnas通过CircRNA-miRNA-mRNA网络调节基因表达的作用研究。在我们的研究中,进行微阵列以检测脂多糖(LPS)诱导的急性呼吸窘迫综合征(ARDS)中Circrnas的表达谱。将20只大鼠随机分为2组,对照组和LPS组,每组10只大鼠。随机选择来自两个组的三只大鼠。使用CircRNA MicroArray数据,我们将肺组织中的Circrna表达谱系与这6只大鼠之间的循环表达曲线进行了比较。来自这些型材的最差异表达的CircrNA物种被验证并优化为ARDS Biomarkers和潜在的治疗靶标。总体而言,395和562个CircrNA分别在LPS组对照组中显着上调。最终选择来自前10名候选者的六个上调和4个下调的Circrnas以进行验证。其中,只有4个上调CircrNA(MMU_CIRCRNA_19423,RNO_CIRCRNA_010489,RNO_CIRCRNA_011426,MMU_CIRCRNA_30664)和1个下调的圆锥(RNO_CIRCRNA_005564)表现出显着的验证。根据miRNA支持向量回归方法预测这5个验证CircrNA的5个最高排名目标miRNA。这是研究Circrna表达谱的第一研究,并且在ARDS期间揭示了大量的异常表达的CircrNA。显着的过度或低于表达的CircrNa可以代表新的生物标志物,并被开发成用于ARDS临床管理的新型治疗靶标。结果是初步的,需要在进一步设计的研究中进行较大的样本尺寸。

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