Abstract

Background Asthma is a common chronic respiratory disease in children, seriously affecting children's health and growth. This bioinformatics study aimed to identify potential RNA candidates closely associated with childhood asthma development within current gene databases. Methods GSE65204 and GSE19187 datasets were screened and downloaded from the NCBI GEO database. Differentially expressed long noncoding RNAs (DE-lncRNAs) and mRNAs (DE-mRNAs) were identified using the Bioconductor limma package in R, and these DE-mRNAs were used to perform biological process (BP) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses. Thereafter, weighted gene coexpression network analysis (WGCNA) was utilized to screen the modules directly related to childhood asthma, and a coexpression network of DE-lncRNAs and DE-mRNAs was built. Finally, principal component analysis (PCA) was performed. Results In total, 7 DE-lncRNAs and 1060 DE-mRNAs, as well as 7 DE-lncRNAs and 1027 DE-mRNAs, were identified in GSE65204 and GSE19187, respectively. After comparison, 336 overlapping genes had the same trend of expression, including 2 overlapped DE-lncRNAs and 334 overlapped DE-mRNAs. These overlapped DE-mRNAs were enriched in 28 BP and 12 KEGG pathways. Eleven modules were obtained in GSE65204, and it was found that the purple, black, and yellow modules were significantly positively correlated with asthma development. Subsequently, a coexpression network including 63 DE-mRNAs and 2 DE-lncRNAs was built, and five KEGG pathways, containing 8 genes, were found to be directly associated with childhood asthma. The PCA further verified these results. Conclusion LncRNAs LINC01559 and SNHG8 and mRNAs VWF, LAMB3, LAMA4, CAV1, ALDH1A3, SMOX, GNG4, and PPARG were identified as biomarkers associated with the progression of childhood asthma.

Highlights

  • Asthma is one of the most common chronic inflammatory respiratory diseases worldwide

  • After functional analysis of genes in the coexpression network, five Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways (“ECM-receptor interaction,” “focal adhesion,” “beta-alanine metabolism,” “PI3K-Akt signaling pathway,” and “pathways in cancer”) contained 8 genes (VWF, laminin subunit beta 3 (LAMB3), laminin subunit alpha 4 (LAMA4), CAV1, aldehyde dehydrogenase 1 family member A3 (ALDH1A3), spermine oxidase (SMOX), G protein subunit gamma 4 (GNG4), and peroxisome proliferatoractivated receptor gamma (PPARG)) which were found to be directly related to childhood asthma development and have potential for use as disease progression biomarkers

  • Wang et al indicated that LINC01559 was upregulated in gastric cancer tissues and could stimulate the PI3K-Akt signaling pathway to accelerate the progression of gastric cancer [35]. erefore, we speculate that Long noncoding RNAs (lncRNAs) SNHG8 and LINC01559 may participate in the occurrence and development of childhood asthma by regulating cell proliferation, migration, and PI3K-Akt signaling pathway

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Summary

Introduction

Asthma is one of the most common chronic inflammatory respiratory diseases worldwide. Corticosteroids, ß-agonists, magnesium sulfate, and anticholinergic drugs are the primary medications used for treating childhood asthma [4] These drugs require long-term use, which can contribute to side effects and drug resistance in children. Asthma is a common chronic respiratory disease in children, seriously affecting children’s health and growth. Is bioinformatics study aimed to identify potential RNA candidates closely associated with childhood asthma development within current gene databases. Ereafter, weighted gene coexpression network analysis (WGCNA) was utilized to screen the modules directly related to childhood asthma, and a coexpression network of DE-lncRNAs and DE-mRNAs was built. A coexpression network including 63 DE-mRNAs and 2 DE-lncRNAs was built, and five KEGG pathways, containing 8 genes, were found to be directly associated with childhood asthma. LncRNAs LINC01559 and SNHG8 and mRNAs VWF, LAMB3, LAMA4, CAV1, ALDH1A3, SMOX, GNG4, and PPARG were identified as biomarkers associated with the progression of childhood asthma

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