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pmid:40074804

Identification and verification of biomarkers associated with arachidonic acid metabolism in non-alcoholic fatty liver disease.

Jia Li · Wei-Wei Su · Zhen-Li Wang · Xiang-Fen Ji · Jing-Wei Wang · Kai Wang

Scientific reports · 2025 doi:10.1038/s41598-025-92972-z

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:40074804
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2026-11-01T20:30:17Z
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paper object · 10 fields
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title
Identification and verification of biomarkers associated with arachidonic acid metabolism in non-alcoholic fatty liver disease.
doi
10.1038/s41598-025-92972-z
pmid
40074804
authors array · 6 items
[0]
Jia Li
[1]
Wei-Wei Su
[2]
Zhen-Li Wang
[3]
Xiang-Fen Ji
[4]
Jing-Wei Wang
[5]
Kai Wang
journal
Scientific reports
year
2025
abstract
Elevated arachidonic acid metabolism (AAM) has been linked to the progression of non-alcoholic fatty liver disease (NAFLD). However, the specific role of AAM-related genes (AAMRGs) in NAFLD remains poorly understood. To investigate the involvement of AAMRGs in NAFLD, this study analyzed datasets GSE89632 and GSE135251 from the Gene Expression Omnibus (GEO) and Molecular Signatures Database (MSigDB). Differential expression analysis revealed 2256 differentially expressed genes (DEGs) between NAFLD and control liver tissues. Cross-referencing these DEGs with AAMRGs identified nine differentially expressed AAMRGs (DE-AAMRGs). Least absolute shrinkage and selection operator (LASSO) and univariate logistic regression analyses pinpointed five biomarkers-CYP2U1, GGT1, PLA2G1B, GPX2, and PTGS1-demonstrating significant diagnostic potential for NAFLD, as validated by receiver operating characteristic (ROC) analysis. These biomarkers were implicated in pathways related to AAM and arachidonate transport. An upstream regulatory network, involving transcription factors (TFs) and MicroRNAs (miRNAs), was constructed to explore the regulatory mechanisms of these biomarkers. In vivo validation using a NAFLD mouse model revealed liver histopathological changes, and quantitative reverse transcription polymerase chain reaction (qRT-PCR) and western blot (WB) analyses confirmed the upregulation of biomarker expression, particularly PTGS1, in NAFLD. The bioinformatic analysis identified five AAM-related biomarkers, enhancing the understanding of NAFLD pathogenesis and offering potential diagnostic targets.
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Gene expression data from NAFLD and CTL samples in GSE89632 were extracted and analyzed to identify DEGs using the limma package (version 3.46.0; date of use: 2023.7.4)51, with thresholds set at |log2FC| > 0.5 and adj P < 0.05.
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sections[11] "Differential expression analysis, enrichment analyses, and PPI analysis" paragraph 2
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Gene expression data from NAFLD and CTL samples in GSE89632 were extracted and analyzed to identify DEGs using the limma package (version 3.46.0; date of use: 2023.7.4)51, with thresholds set at |log2FC| > 0.5 and adj P < 0.05.
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sections[23] "notes" paragraph 1
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The datasets analysed during the current study are available in the (GEO)repository, (https://www.ncbi.nlm.nih.gov/gds). The experimental data in this study is available from the corresponding author on request.
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The study identified five arachidonic acid metabolism-related biomarkers with diagnostic potential for NAFLD and validated their expression in an in vivo NAFLD mouse model.
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The bioinformatic analysis identified five AAM-related biomarkers, enhancing the understanding of NAFLD pathogenesis and offering potential diagnostic targets.
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The study identified five arachidonic acid metabolism-related biomarkers with diagnostic potential for NAFLD and validated their expression in an in vivo NAFLD mouse model.
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TRANSCRIPTOMIC PROFILING ACROSS THE SPECTRUM OF NON-ALCOHOLIC FATTY LIVER DISEASE
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Genome-wide analysis of hepatic gene expression in patients with non-alcoholic fatty liver disease and in healthy donors in relation to hepatic fatty acid composition and other nutritional factors
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biomarkers. In vivo validation using a NAFLD mouse model revealed liver histopathological changes, an
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e regulatory mechanisms of these biomarkers. In vivo validation using a NAFLD mouse model reveale
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biomarkers. In vivo validation using a NAFLD mouse model revealed liver histopathological chang
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Methods NAFLD mouse model construction and sample collection Efforts w
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tion polymerase chain reaction (qRT-PCR) and western blot (WB) analyses confirmed the upregulation of
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Gene expression data from NAFLD and CTL samples in GSE89632 were extracted and analyzed to identify DEGs using the limma package (version 3.46.0; date of use: 2023.7.4)51, with thresholds set at |log2FC| > 0.5 and adj P < 0.05.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40074804", "kind": "science-record", "revision": 4, "content_hash": "sha256:6ac24405a06cef59d93c8c12dea8c828d15842745858037efaa7a7b291645ffc", "created_at": "2026-11-01T20:30:17Z", "updated_at": "2026-11-01T22:56:13Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and verification of biomarkers associated with arachidonic acid metabolism in non-alcoholic fatty liver disease.", "doi": "10.1038/s41598-025-92972-z", "pmid": "40074804", "authors": ["Jia Li", "Wei-Wei Su", "Zhen-Li Wang", "Xiang-Fen Ji", "Jing-Wei Wang", "Kai Wang"], "journal": "Scientific reports", "year": 2025, "abstract": "Elevated arachidonic acid metabolism (AAM) has been linked to the progression of non-alcoholic fatty liver disease (NAFLD). However, the specific role of AAM-related genes (AAMRGs) in NAFLD remains poorly understood. To investigate the involvement of AAMRGs in NAFLD, this study analyzed datasets GSE89632 and GSE135251 from the Gene Expression Omnibus (GEO) and Molecular Signatures Database (MSigDB). Differential expression analysis revealed 2256 differentially expressed genes (DEGs) between NAFLD and control liver tissues. Cross-referencing these DEGs with AAMRGs identified nine differentially expressed AAMRGs (DE-AAMRGs). Least absolute shrinkage and selection operator (LASSO) and univariate logistic regression analyses pinpointed five biomarkers-CYP2U1, GGT1, PLA2G1B, GPX2, and PTGS1-demonstrating significant diagnostic potential for NAFLD, as validated by receiver operating characteristic (ROC) analysis. These biomarkers were implicated in pathways related to AAM and arachidonate transport. An upstream regulatory network, involving transcription factors (TFs) and MicroRNAs (miRNAs), was constructed to explore the regulatory mechanisms of these biomarkers. In vivo validation using a NAFLD mouse model revealed liver histopathological changes, and quantitative reverse transcription polymerase chain reaction (qRT-PCR) and western blot (WB) analyses confirmed the upregulation of biomarker expression, particularly PTGS1, in NAFLD. 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