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pmid:39920823

Analysis of long noncoding gene expression and its interactions with protein-coding genes in vascular endothelial cells in keloids.

Yunxiang Luo · Zi Ye · Yi Li · Chau Wei Wong · Shuqia Xu · Yu Deng · Zhicheng Su · Xueqing Li · Yingxiong Huang · Bing Han

European journal of medical research · 2025 doi:10.1186/s40001-025-02271-6

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complete

Experiment

complete

Data

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Analysis

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Execution

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title
Analysis of long noncoding gene expression and its interactions with protein-coding genes in vascular endothelial cells in keloids.
doi
10.1186/s40001-025-02271-6
pmid
39920823
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Yunxiang Luo
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Zi Ye
[2]
Yi Li
[3]
Chau Wei Wong
[4]
Shuqia Xu
[5]
Yu Deng
[6]
Zhicheng Su
[7]
Xueqing Li
[8]
Yingxiong Huang
[9]
Bing Han
journal
European journal of medical research
year
2025
abstract
OBJECTIVES: The purpose of this study was to determine the relationship between protein-coding RNA (messenger RNA, mRNA) and long noncoding RNA (lncRNA) expressed in vascular endothelial cells (VECs) in keloids by reanalyzing Gene Expression Omnibus (GEO) microarray chip data. MATERIALS AND METHODS: The GSE121618 database and clinical information of these samples were downloaded and reanalyzed by the R language package. Expression differences in mRNA and lncRNA between keloids and normal skin were calculated. GO/KEGG enrichment analysis was conducted to determine the function of these genes, and an interaction network of lncRNAs-mRNAs was constructed. Magnetic Sorting of VECs and qRT-PCR were used to verify these bioinformatic results. RESULTS: The expression of three hundred and five mRNAs in the keloid group was significantly different from that in the normal group, and 98 lncRNAs were different, 21 of which were upregulated and 118 of which were downregulated. The hub relationship between the upregulated lncRNA‒mRNA interaction was lncRNA LINC01546-RASAL3/COL13A1, while the downregulated hub was lncRNA LOC101929787-PRKAA2/KRT71/SSTR1. qPCR verification result showed no obvious statistical differences. CONCLUSIONS: Through the in-depth mining of keloid microarray data using bioinformatic methods, we speculated that VECs can affect the development and progression of keloids by epigenomic regulation via lncRNA‒mRNA interactions.
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R package limma were chosen to perform gene differential expression analysis. The cut off of significant differential expressed mRNA and lncRNA were set as abs (fold changes) > 1.5 and P.adjust < 0.05 and filtered out differentially expressed mRNAs (DEmRNAs) and lncRNAs (DElncRNAs) were obtained. DEmRNAs were chosen as the candidate genelist, and the significance level of each GO/KEGG term was calculated using the Fisher test. First, the Pearson correlation coefficient (PCC) among DElncRNA and DEmRNA were calculated, and PCC > 0.95 were used as the cutoff threshold of significant DEmRNA–DElncRNA correlated pairs.
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R package limma were chosen to perform gene differential expression analysis.
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The cut off of significant differential expressed mRNA and lncRNA were set as abs (fold changes) > 1.5 and P.adjust < 0.05 and filtered out differentially expressed mRNAs (DEmRNAs) and lncRNAs (DElncRNAs) were obtained.
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The expression of 305 mRNAs and 98 lncRNAs was significantly different in keloid VECs compared with normal-skin VECs.
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The expression of three hundred and five mRNAs in the keloid group was significantly different from that in the normal group, and 98 lncRNAs were different, 21 of which were upregulated and 118 of which were downregulated.
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Expression Profile of Isolated Endothelial cells in Human Keloids: A microarray analysis
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by reanalyzing Gene Expression Omnibus (GEO) microarray chip data. MATERIALS AND METHODS: The GSE121
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Complete file
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Expression differences in mRNA and lncRNA between keloids and normal skin were calculated. GO/KEGG enrichment analysis was conducted to determine the function of these genes, and an interaction network of lncRNAs-mRNAs was constructed. Magnetic Sorting of VECs and qRT-PCR were used to verify these bioinformatic results.\nRESULTS: The expression of three hundred and five mRNAs in the keloid group was significantly different from that in the normal group, and 98 lncRNAs were different, 21 of which were upregulated and 118 of which were downregulated. The hub relationship between the upregulated lncRNA‒mRNA interaction was lncRNA LINC01546-RASAL3/COL13A1, while the downregulated hub was lncRNA LOC101929787-PRKAA2/KRT71/SSTR1. qPCR verification result showed no obvious statistical differences.\nCONCLUSIONS: Through the in-depth mining of keloid microarray data using bioinformatic methods, we speculated that VECs can affect the development and progression of keloids by epigenomic regulation via lncRNA‒mRNA interactions.", "claims": [{"id": "claim-method", "statement": "R package limma were chosen to perform gene differential expression analysis. The cut off of significant differential expressed mRNA and lncRNA were set as abs (fold changes) > 1.5 and P.adjust < 0.05 and filtered out differentially expressed mRNAs (DEmRNAs) and lncRNAs (DElncRNAs) were obtained. DEmRNAs were chosen as the candidate genelist, and the significance level of each GO/KEGG term was calculated using the Fisher test. 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