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pmid:33832098
Identification and validation of key non-coding RNAs and mRNAs using co-expression network analysis in pre-eclampsia.
Jing He · Kang Liu · Xiaohong Hou · Jieqiang Lu
Medicine · 2021 doi:10.1097/MD.0000000000025294
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Experiment
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Complete file
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In this study, we aimed to explore important long non-coding RNAs (lncRNAs) and their possible mechanisms in PE.GSE60438 expression profile including 25 PE samples and 23 normal samples were obtained from gene expression omnibus (GEO) database. After normalization with betaqn package in R, differentially expressed lncRNAs (DElncRNAs) and mRNAs (DEmRNAs) were identified using the limma package. Gene Ontology (GO) and Kyoto encyclopedia of genes and genomes (KEGG) pathway were analyzed using DAVID 6.7 and GSEA 3.0. LncRNAs-mRNAs coexpression was implemented using weighted gene co-expression network analysis (WGCNA). MicroRNAs linked with these DElncRNAs and DEmRNAs were predicted and a competitive endogenous RNA (ceRNA) network was built.A total of 53 DElncRNAs and 301 DEmRNAs were identified between control and PE samples. These DEmRNAs were enriched into pathways such as protein digestion and absorption, osteoclast differentiation. WGCNA constructed a lncRNA-mRNA coexpression network, among which SUMO1P3, NACAP1, NCF1C, ANXA2P1, GTF2IP1, NAPSB, OR7E37P were hub genes. ceRNA network was constructed together with microRNAs (miRNAs), and functional analysis indicated cellular membrane and sugar binding were involved in PE progression. Five lncRNAsANXA2P1, GTF2IP1, NACAP1, NCF1C and OR7E37P were successfully validated in our clinical specimens.The DElncRNAs, including ANXA2P1, GTF2IP1, NACAP1, NCF1C and OR7E37P might play important roles in PE. However, the exact mechanism of these lncRNAs in prediction and diagnosis of PE should be further explored.", "claims": [{"id": "claim-method", "statement": "Further, differential gene expression analysis was implemented using the limma package (version 3.10.3) in R. 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The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE60438"], "resolved_accessions": ["GSE60438"], "statements": ["The raw data of expression profile of GSE60438 based on platforms of GPL6884 and GPL10558 were obtained from the gene expression omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo/). This dataset included genome-wide transcriptome sequencing data on 65 normotensive and 60 PE patients and was contributed by Yong et al.[14] The sequencing data based on the platform of GPL6884, which included 48 samples from 25 PE samples and 23 normal samples, were extracted for further analysis."], "basis": "The paper names GSE60438 in gene expression omnibus (GEO) database and the accession resolves in the repository. 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