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通过生物信息学分析对扩张型心肌病中长链非编码RNA进行鉴定及功能预测

Identification and Functional Prediction of Long Non-Coding RNAs in Dilated Cardiomyopathy by Bioinformatics Analysis.

作者信息

Chen Yu-Xiao, Ding Jie, Zhou Wei-Er, Zhang Xuan, Sun Xiao-Tong, Wang Xi-Ying, Zhang Chi, Li Ni, Shao Guo-Feng, Hu Shen-Jiang, Yang Jian

机构信息

The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Ningbo Medical Center Lihuili Hospital, Ningbo, China.

出版信息

Front Genet. 2021 Apr 16;12:648111. doi: 10.3389/fgene.2021.648111. eCollection 2021.

Abstract

Dilated cardiomyopathy (DCM) is a relatively common cause of heart failure and the leading cause of heart transplantation. Aberrant changes in long non-coding RNAs (lncRNAs) are involved in DCM disorder; however, the detailed mechanisms underlying DCM initiation and progression require further investigation, and new molecular targets are needed. Here, we obtained lncRNA-expression profiles associated with DCM and non-failing hearts through microarray probe-sequence re-annotation. Weighted gene co-expression network analysis revealed a module highly associated with DCM status. Then eight hub lncRNAs in this module (FGD5-AS1, AC009113.1, WDFY3-AS2, NIFK-AS1, ZNF571-AS1, MIR100HG, AC079089.1, and EIF3J-AS1) were identified. All hub lncRNAs except ZNF571-AS1 were predicted as localizing to the cytoplasm. As a possible mechanism of DCM pathogenesis, we predicted that these hub lncRNAs might exert functions by acting as competing endogenous RNAs (ceRNAs). Furthermore, we found that the above results can be essentially reproduced in an independent external dataset. We observed the localization of hub lncRNAs by RNA-FISH in human aortic smooth muscle cells and confirmed the upregulation of the hub lncRNAs in DCM patients through quantitative RT-PCR. In conclusion, these findings identified eight candidate lncRNAs associated with DCM disease and revealed their potential involvement in DCM partly through ceRNA crosstalk. Our results facilitate the discovery of therapeutic targets and enhance the understanding of DCM pathogenesis.

摘要

扩张型心肌病(DCM)是心力衰竭的相对常见病因,也是心脏移植的主要原因。长链非编码RNA(lncRNA)的异常变化参与了DCM疾病;然而,DCM发生和发展的详细机制仍需进一步研究,并且需要新的分子靶点。在这里,我们通过微阵列探针序列重新注释获得了与DCM和非衰竭心脏相关的lncRNA表达谱。加权基因共表达网络分析揭示了一个与DCM状态高度相关的模块。然后在该模块中鉴定出八个枢纽lncRNA(FGD5-AS1、AC009113.1、WDFY3-AS2、NIFK-AS1、ZNF571-AS1、MIR100HG、AC079089.1和EIF3J-AS1)。除ZNF571-AS1外,所有枢纽lncRNA均被预测定位于细胞质。作为DCM发病机制的一种可能机制,我们预测这些枢纽lncRNA可能通过作为竞争性内源RNA(ceRNA)发挥作用。此外,我们发现上述结果在一个独立的外部数据集中基本可以重现。我们通过RNA-FISH在人主动脉平滑肌细胞中观察了枢纽lncRNA的定位,并通过定量RT-PCR证实了DCM患者中枢纽lncRNA的上调。总之,这些发现鉴定了八个与DCM疾病相关的候选lncRNA,并揭示了它们可能部分通过ceRNA串扰参与DCM。我们的结果有助于发现治疗靶点并增进对DCM发病机制的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0da9/8085533/3fbd9485c78d/fgene-12-648111-g001.jpg

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