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Title:
Identification and Validation of Ferroptosis-Related Genes in Patients with Acute Spinal Cord Injury | Molecular Neurobiology
Description:
Ferroptosis plays crucial roles in the pathology of spinal cord injury (SCI). The purpose of this study was to identify differentially expressed ferroptosis-related genes (DE-FRGs) in human acute SCI by bioinformatics analysis and validate the hub DE-FRGs in non-SCI and SCI patients. The GSE151371 dataset was downloaded from the Gene Expression Omnibus and difference analysis was performed. The differentially expressed genes (DEGs) in GSE151371 overlapped with the ferroptosis-related genes (FRGs) obtained from the Ferroptosis Database. A total of 41 DE-FRGs were detected in 38 SCI samples and 10 healthy samples in GSE151371. Then, enrichment analyses of these DE-FRGs were performed for functional annotation. The GO enrichment results showed that upregulated DE-FRGs were mainly associated with reactive oxygen species and redox reactions, and the KEGG enrichment analysis indicated involvement in some diseases and ferroptosis pathways. Protein-protein interaction (PPI) analysis and lncRNA-miRNA-mRNA regulatory network were performed to explore the correlations between genes and regulatory mechanisms. The relationship between DE-FRGs and differentially expressed mitochondria-related genes (DE-MRGs) was also analyzed. Finally, quantitative real-time polymerase chain reaction (qRT-PCR) was used to verify the hub DE-FRGs in clinical blood samples from acute SCI patients and healthy controls. Consistent with the bioinformatics results, qRT-PCR of the clinical samples indicated similar expression levels of TLR4, STAT3, and HMOX1. This study identified DE-FRGs in blood samples from SCI patients, and the results could improve our understanding of the molecular mechanisms of ferroptosis in SCI. These candidate genes and pathways could be therapeutic targets for SCI.
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Keywords {π}
pubmed, article, google, scholar, cas, injury, spinal, cord, central, zhang, ferroptosis, cell, genes, sci, analysis, res, yang, functional, recovery, liu, httpsdoiorg, qingdao, data, ferroptosisrelated, defrgs, chen, study, bioinformatics, gene, traumatic, brain, information, research, acute, jia, mechanisms, access, biol, httpsdoiorgs, promotes, authors, privacy, cookies, content, consent, identification, validation, patients, chao, performed,
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microrna-130b-5p/tlr4/nf-ΞΊb axis mir-135b-5p/tgf-Ξ²r1 axis large-scale clip-seq data month download article/chapter lncrna-mirna-mrna regulatory network targeting mir-34a-5p combines cuproptosis-related genes genome-wide transcriptome analysis protein-rna interaction networks gov/geo/query/acc ferroptosis-related genes participate gene set analysis gene expression omnibus full article pdf di paolo ml differentially expressed genes nf-ΞΊb signaling reactive oxygen species haitao fu designed microglia-induced neuroinflammation privacy choices/manage cookies spinal cord injury health research program dixon sj microrna binding sites holds exclusive rights supplementary information files ferroptosis-related genes study identified de-frgs human acute sci spinal cord injuries article qu promotes functional recovery similar expression levels zinc attenuates ferroptosis ef24 induces ferroptosis protein-protein interaction improves functional recovery die hu contributed kegg enrichment analysis programmed cell death nonapoptotic cell death individual participants included deferoxamine promotes recovery traumatic brain injury ischemic brain injury decoding mirna-cerna additional information publisher time points pi3k/akt pathway
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headline:Identification and Validation of Ferroptosis-Related Genes in Patients with Acute Spinal Cord Injury
description:Ferroptosis plays crucial roles in the pathology of spinal cord injury (SCI). The purpose of this study was to identify differentially expressed ferroptosis-related genes (DE-FRGs) in human acute SCI by bioinformatics analysis and validate the hub DE-FRGs in non-SCI and SCI patients. The GSE151371 dataset was downloaded from the Gene Expression Omnibus and difference analysis was performed. The differentially expressed genes (DEGs) in GSE151371 overlapped with the ferroptosis-related genes (FRGs) obtained from the Ferroptosis Database. A total of 41 DE-FRGs were detected in 38 SCI samples and 10 healthy samples in GSE151371. Then, enrichment analyses of these DE-FRGs were performed for functional annotation. The GO enrichment results showed that upregulated DE-FRGs were mainly associated with reactive oxygen species and redox reactions, and the KEGG enrichment analysis indicated involvement in some diseases and ferroptosis pathways. Protein-protein interaction (PPI) analysis and lncRNA-miRNA-mRNA regulatory network were performed to explore the correlations between genes and regulatory mechanisms. The relationship between DE-FRGs and differentially expressed mitochondria-related genes (DE-MRGs) was also analyzed. Finally, quantitative real-time polymerase chain reaction (qRT-PCR) was used to verify the hub DE-FRGs in clinical blood samples from acute SCI patients and healthy controls. Consistent with the bioinformatics results, qRT-PCR of the clinical samples indicated similar expression levels of TLR4, STAT3, and HMOX1. This study identified DE-FRGs in blood samples from SCI patients, and the results could improve our understanding of the molecular mechanisms of ferroptosis in SCI. These candidate genes and pathways could be therapeutic targets for SCI.
datePublished:2023-06-14T00:00:00Z
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Quantitative real-time polymerase chain reaction
Neurosciences
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headline:Identification and Validation of Ferroptosis-Related Genes in Patients with Acute Spinal Cord Injury
description:Ferroptosis plays crucial roles in the pathology of spinal cord injury (SCI). The purpose of this study was to identify differentially expressed ferroptosis-related genes (DE-FRGs) in human acute SCI by bioinformatics analysis and validate the hub DE-FRGs in non-SCI and SCI patients. The GSE151371 dataset was downloaded from the Gene Expression Omnibus and difference analysis was performed. The differentially expressed genes (DEGs) in GSE151371 overlapped with the ferroptosis-related genes (FRGs) obtained from the Ferroptosis Database. A total of 41 DE-FRGs were detected in 38 SCI samples and 10 healthy samples in GSE151371. Then, enrichment analyses of these DE-FRGs were performed for functional annotation. The GO enrichment results showed that upregulated DE-FRGs were mainly associated with reactive oxygen species and redox reactions, and the KEGG enrichment analysis indicated involvement in some diseases and ferroptosis pathways. Protein-protein interaction (PPI) analysis and lncRNA-miRNA-mRNA regulatory network were performed to explore the correlations between genes and regulatory mechanisms. The relationship between DE-FRGs and differentially expressed mitochondria-related genes (DE-MRGs) was also analyzed. Finally, quantitative real-time polymerase chain reaction (qRT-PCR) was used to verify the hub DE-FRGs in clinical blood samples from acute SCI patients and healthy controls. Consistent with the bioinformatics results, qRT-PCR of the clinical samples indicated similar expression levels of TLR4, STAT3, and HMOX1. This study identified DE-FRGs in blood samples from SCI patients, and the results could improve our understanding of the molecular mechanisms of ferroptosis in SCI. These candidate genes and pathways could be therapeutic targets for SCI.
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