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COPD 中的基因表达网络:miRNA 和 mRNA 调控。

Gene expression networks in COPD: microRNA and mRNA regulation.

机构信息

Department of Medicine, Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University Medical Center, Columbus, Ohio 43210, USA.

出版信息

Thorax. 2012 Feb;67(2):122-31. doi: 10.1136/thoraxjnl-2011-200089. Epub 2011 Sep 22.

Abstract

BACKGROUND

The mechanisms underlying chronic obstructive pulmonary disease (COPD) remain unclear. MicroRNAs (miRNAs or miRs) are small non-coding RNA molecules that modulate the levels of specific genes and proteins. Identifying expression patterns of miRNAs in COPD may enhance our understanding of the mechanisms of disease. A study was undertaken to determine if miRNAs are differentially expressed in the lungs of smokers with and without COPD. miRNA and mRNA expression were compared to enrich for biological networks relevant to the pathogenesis of COPD.

METHODS

Lung tissue from smokers with no evidence of obstructive lung disease (n=9) and smokers with COPD (n=26) was examined for miRNA and mRNA expression followed by validation. We then examined both miRNA and mRNA expression to enrich for relevant biological pathways.

RESULTS

70 miRNAs and 2667 mRNAs were differentially expressed between lung tissue from subjects with COPD and smokers without COPD. miRNA and mRNA expression profiles enriched for biological pathways that may be relevant to the pathogenesis of COPD including the transforming growth factor β, Wnt and focal adhesion pathways. miR-223 and miR-1274a were the most affected miRNAs in subjects with COPD compared with smokers without obstruction. miR-15b was increased in COPD samples compared with smokers without obstruction and localised to both areas of emphysema and fibrosis. miR-15b was differentially expressed within GOLD classes of COPD. Expression of SMAD7, which was validated as a target for miR-15b, was decreased in bronchial epithelial cells in COPD.

CONCLUSIONS

miRNA and mRNA are differentially expressed in individuals with COPD compared with smokers without obstruction. Investigating these relationships may further our understanding of the mechanisms of disease.

摘要

背景

慢性阻塞性肺疾病(COPD)的发病机制仍不清楚。微小 RNA(miRNA 或 miR)是一种小的非编码 RNA 分子,可调节特定基因和蛋白质的水平。鉴定 COPD 患者肺部 miRNA 的表达模式可能有助于我们了解疾病的发病机制。本研究旨在确定 miRNA 是否在无阻塞性肺疾病的吸烟者和 COPD 患者的肺部存在差异表达。比较 miRNA 和 mRNA 的表达以富集与 COPD 发病机制相关的生物学网络。

方法

检查无阻塞性肺疾病的吸烟者(n=9)和 COPD 吸烟者(n=26)的肺组织中的 miRNA 和 mRNA 表达情况,然后进行验证。我们随后检查了 miRNA 和 mRNA 的表达情况,以富集相关的生物学途径。

结果

COPD 患者和无 COPD 吸烟者的肺组织中 70 个 miRNA 和 2667 个 mRNA 表达存在差异。miRNA 和 mRNA 表达谱富集了可能与 COPD 发病机制相关的生物学途径,包括转化生长因子 β、Wnt 和黏附斑途径。与无阻塞的吸烟者相比,COPD 患者的 miR-223 和 miR-1274a 是受影响最严重的 miRNA。与无阻塞的吸烟者相比,COPD 样本中的 miR-15b 增加,并且定位于肺气肿和纤维化区域。miR-15b 在 COPD 的 GOLD 分级中存在差异表达。SMAD7 的表达被验证为 miR-15b 的靶标,在 COPD 的支气管上皮细胞中减少。

结论

与无阻塞的吸烟者相比,COPD 患者的 miRNA 和 mRNA 表达存在差异。研究这些关系可能有助于我们进一步了解疾病的发病机制。

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