Identification of Potential lncRNA-miRNA-mRNA Regulatory Network Contributing to Arrhythmogenic Right Ventricular Cardiomyopathy
Open Access
- 30 May 2024
- journal article
- research article
- Published by MDPI AG in Journal of Cardiovascular Development and Disease
- Vol. 11 (6) , 168
Abstract
Arrhythmogenic right ventricular cardiomyopathy (ARVC) can lead to sudden cardiac death and life-threatening heart failure. Due to its high fatality rate and limited therapies, the pathogenesis and diagnosis biomarker of ARVC needs to be explored urgently. This study aimed to explore the lncRNA-miRNA-mRNA competitive endogenous RNA (ceRNA) network in ARVC. The mRNA and lncRNA expression datasets obtained from the Gene Expression Omnibus (GEO) database were used to analyze differentially expressed mRNA (DEM) and lncRNA (DElnc) between ARVC and non-failing controls. Differentially expressed miRNAs (DEmiRs) were obtained from the previous profiling work. Using starBase to predict targets of DEmiRs and intersecting with DEM and DElnc, a ceRNA network of lncRNA-miRNA-mRNA was constructed. The DEM and DElnc were validated by real-time quantitative PCR in human heart tissue. Protein–protein interaction network and weighted gene co-expression network analyses were used to identify hub genes. A logistic regression model for ARVC diagnostic prediction was established with the hub genes and their ceRNA pairs in the network. A total of 448 DEMs (282 upregulated and 166 downregulated) were identified, mainly enriched in extracellular matrix and fibrosis-related GO terms and KEGG pathways, such as extracellular matrix organization and collagen fibril organization. Four mRNAs and two lncRNAs, including COL1A1, COL5A1, FBN1, BGN, XIST, and LINC00173 identified through the ceRNA network, were validated by real-time quantitative PCR in human heart tissue and used to construct a logistic regression model. Good ARVC diagnostic prediction performance for the model was shown in both the training set and the validation set. The potential lncRNA-miRNA-mRNA regulatory network and logistic regression model established in our study may provide promising diagnostic methods for ARVC.Keywords
Funding Information
- National Key Research and Development Program of China (2016YFC1300901, 31801068)
- National Natural Science Foundation of China (2016YFC1300901, 31801068)
This publication has 39 references indexed in Scilit:
- Insights Into Genetics and Pathophysiology of Arrhythmogenic CardiomyopathyCurrent Heart Failure Reports, 2021
- Type V Collagen in Scar Tissue Regulates the Size of Scar after Heart InjuryCell, 2020
- Increased frequency of FBN1 frameshift and nonsense mutations in Marfan syndrome patients with aortic dissectionMolecular Genetics & Genomic Medicine, 2019
- Clinical Diagnosis, Imaging, and Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy/DysplasiaJACC, 2018
- Comprehensive Myocardial Proteogenomics Profiling Reveals C/EBPα as the Key Factor in the Lipid Storage of ARVCJournal of Proteome Research, 2017
- MiR-320a as a Potential Novel Circulating Biomarker of Arrhythmogenic CardioMyopathyScientific Reports, 2017
- Arrhythmogenic Right Ventricular CardiomyopathyNew England Journal of Medicine, 2017
- Profiling of differentially expressed microRNAs in arrhythmogenic right ventricular cardiomyopathyScientific Reports, 2016
- The multilayered complexity of ceRNA crosstalk and competitionNature, 2014
- Regulatory mutations in transforming growth factor-?3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1Cardiovascular Research, 2005