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pmid:37081490

Identification of ferroptosis-related genes in male mice with sepsis-induced acute lung injury based on transcriptome sequencing.

Wen Hu · Zhen Wu · Mei Zhang · Shilin Yu · Xiaohua Zou

BMC pulmonary medicine · 2023 doi:10.1186/s12890-023-02361-3

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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title
Identification of ferroptosis-related genes in male mice with sepsis-induced acute lung injury based on transcriptome sequencing.
doi
10.1186/s12890-023-02361-3
pmid
37081490
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Wen Hu
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Zhen Wu
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Mei Zhang
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Shilin Yu
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Xiaohua Zou
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BMC pulmonary medicine
year
2023
abstract
BACKGROUND: Sepsis can result in acute lung injury (ALI). Studies have shown that pharmacological inhibition of ferroptosis can treat ALI. However, the regulatory mechanisms of ferroptosis in sepsis-induced ALI remain unclear. METHODS: Transcriptome sequencing was performed on lung tissue samples from 10 sepsis-induced mouse models of ALI and 10 control mice. After quality control measures, clean data were used to screen for differentially expressed genes (DEGs) between the groups. The DEGs were then overlapped with ferroptosis-related genes (FRGs) to obtain ferroptosis-related DEGs (FR-DEGs). Subsequently, least absolute shrinkage and selection operator (Lasso) and Support Vector Machine-Recursive Feature Elimination (SVM-RFE) were used to obtain key genes. In addition, Ingenuity Pathway Analysis (IPA) was employed to explore the disease, function, and canonical pathways related to the key genes. Gene set enrichment analysis (GSEA) was used to investigate the functions of the key genes, and regulatory miRNAs of key genes were predicted using the NetworkAnalyst and StarBase databases. Finally, the expression of key genes was validated with the GSE165226 and GSE168796 datasets sourced from the Gene Expression Omnibus (GEO) database and using quantitative real-time polymerase chain reaction (qRT-PCR). RESULTS: Thirty-three FR-DEGs were identified between 1843 DEGs and 259 FRGs. Three key genes, Ncf2, Steap3, and Gclc, were identified based on diagnostic models established by the two machine learning methods. They are mainly involved in infection, immunity, and apoptosis, including lymphatic system cell migration and lymphocyte and T cell responses. Additionally, the GSEA suggested that Ncf2 and Steap3 were similarly enriched in mRNA processing, response to peptides, and leukocyte differentiation. Furthermore, a key gene-miRNA network including 2 key genes (Steap3 and Gclc) and 122 miRNAs, and a gene-miRNA network with 1 key gene (Steap3) and 3 miRNAs were constructed using NetworkAnalyst and StarBase, respectively. Both databases predicted that mmu-miR-15a-5p was the target miRNA of Steap3. Finally, Ncf2 expression was validated using both datasets and qRT-PCR, and Steap3 was validated using GSE165226 and qRT-PCR. CONCLUSIONS: This study identified two FR-DEGs (Ncf2 and Steap3) associated with sepsis-induced ALI via transcriptome analyses, as well as their functional and metabolic pathways.
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The t-test was utilized to contrast the expression differences of the FR-DEGs and key genes between sepsis-induced ALI and control samples.
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Transcriptome-based statistical analysis identified Ncf2 and Steap3 as ferroptosis-related differentially expressed genes associated with sepsis-induced acute lung injury.
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This study identified two FR-DEGs (Ncf2 and Steap3) associated with sepsis-induced ALI via transcriptome analyses, as well as their functional and metabolic pathways.
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n lung tissue samples from 10 sepsis-induced mouse models of ALI and 10 control mice. After qua
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37081490", "kind": "science-record", "revision": 3, "content_hash": "sha256:fb0718d2234fab4566932f214e3ea046a7aa1bd529dd62ba1d90287eed71a64d", "created_at": "2026-11-01T19:01:44Z", "updated_at": "2026-11-01T22:09:17Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of ferroptosis-related genes in male mice with sepsis-induced acute lung injury based on transcriptome sequencing.", "doi": "10.1186/s12890-023-02361-3", "pmid": "37081490", "authors": ["Wen Hu", "Zhen Wu", "Mei Zhang", "Shilin Yu", "Xiaohua Zou"], "journal": "BMC pulmonary medicine", "year": 2023, "abstract": "BACKGROUND: Sepsis can result in acute lung injury (ALI). Studies have shown that pharmacological inhibition of ferroptosis can treat ALI. However, the regulatory mechanisms of ferroptosis in sepsis-induced ALI remain unclear.\nMETHODS: Transcriptome sequencing was performed on lung tissue samples from 10 sepsis-induced mouse models of ALI and 10 control mice. After quality control measures, clean data were used to screen for differentially expressed genes (DEGs) between the groups. The DEGs were then overlapped with ferroptosis-related genes (FRGs) to obtain ferroptosis-related DEGs (FR-DEGs). Subsequently, least absolute shrinkage and selection operator (Lasso) and Support Vector Machine-Recursive Feature Elimination (SVM-RFE) were used to obtain key genes. In addition, Ingenuity Pathway Analysis (IPA) was employed to explore the disease, function, and canonical pathways related to the key genes. Gene set enrichment analysis (GSEA) was used to investigate the functions of the key genes, and regulatory miRNAs of key genes were predicted using the NetworkAnalyst and StarBase databases. Finally, the expression of key genes was validated with the GSE165226 and GSE168796 datasets sourced from the Gene Expression Omnibus (GEO) database and using quantitative real-time polymerase chain reaction (qRT-PCR).\nRESULTS: Thirty-three FR-DEGs were identified between 1843 DEGs and 259 FRGs. Three key genes, Ncf2, Steap3, and Gclc, were identified based on diagnostic models established by the two machine learning methods. They are mainly involved in infection, immunity, and apoptosis, including lymphatic system cell migration and lymphocyte and T cell responses. Additionally, the GSEA suggested that Ncf2 and Steap3 were similarly enriched in mRNA processing, response to peptides, and leukocyte differentiation. Furthermore, a key gene-miRNA network including 2 key genes (Steap3 and Gclc) and 122 miRNAs, and a gene-miRNA network with 1 key gene (Steap3) and 3 miRNAs were constructed using NetworkAnalyst and StarBase, respectively. Both databases predicted that mmu-miR-15a-5p was the target miRNA of Steap3. Finally, Ncf2 expression was validated using both datasets and qRT-PCR, and Steap3 was validated using GSE165226 and qRT-PCR.\nCONCLUSIONS: This study identified two FR-DEGs (Ncf2 and Steap3) associated with sepsis-induced ALI via transcriptome analyses, as well as their functional and metabolic pathways.", "claims": [{"id": "claim-method", "statement": "The t-test was utilized to contrast the expression differences of the FR-DEGs and key genes between sepsis-induced ALI and control samples.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37081490", "locator": "sections[12] \"Statistical analysis\" paragraph 2", "quote": "The t-test was utilized to contrast the expression differences of the FR-DEGs and key genes between sepsis-induced ALI and control samples."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data analyzed in this manuscript are publicly available from the Sequence Read Archive(https://www.ncbi.nlm.nih.gov/sra/PRJNA899441).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37081490", "locator": "sections[30] \"Availability of data and materials\" paragraph 2", "quote": "Data analyzed in this manuscript are publicly available from the Sequence Read Archive(https://www.ncbi.nlm.nih.gov/sra/PRJNA899441)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Transcriptome-based statistical analysis identified Ncf2 and Steap3 as ferroptosis-related differentially expressed genes associated with sepsis-induced acute lung injury.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37081490", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "This study identified two FR-DEGs (Ncf2 and Steap3) associated with sepsis-induced ALI via transcriptome analyses, as well as their functional and metabolic pathways."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Transcriptome-based statistical analysis identified Ncf2 and Steap3 as ferroptosis-related differentially expressed genes associated with sepsis-induced acute lung injury.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37081490"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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