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pmid:40230692

Machine learning-based transcriptmics analysis reveals BMX, GRB10, and GADD45A as crucial biomarkers and therapeutic targets in sepsis.

Yanwei Cheng · Haoran Peng · Qiao Chen · Lijun Xu · Lijie Qin

Frontiers in pharmacology · 2025 doi:10.3389/fphar.2025.1576467

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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title
Machine learning-based transcriptmics analysis reveals BMX, GRB10, and GADD45A as crucial biomarkers and therapeutic targets in sepsis.
doi
10.3389/fphar.2025.1576467
pmid
40230692
authors array · 5 items
[0]
Yanwei Cheng
[1]
Haoran Peng
[2]
Qiao Chen
[3]
Lijun Xu
[4]
Lijie Qin
journal
Frontiers in pharmacology
year
2025
abstract
Sepsis is a life-threatening condition characterized by a dysregulated host response to infection, resulting in high mortality rates and complex clinical management. This study leverages transcriptomics and machine learning (ML) to identify critical biomarkers and therapeutic targets in sepsis. Analyzing microarray data from the Gene Expression Omnibus (GEO) datasets GSE28750, GSE26440, GSE13205, and GSE9960, we discovered three pivotal biomarkers that BMX (bone marrow tyrosine kinase gene on chromosome X), GRB10 (growth factor receptor bound protein 10), and GADD45A (growth arrest and DNA damage inducible alpha), exhibiting exceptional diagnostic accuracy (AUC >0.9). Functional enrichment analyses revealed that these genes play key roles in reactive oxygen species metabolism and immune response regulation. Specifically, GADD45A was positively correlated with eosinophils and inversely associated with activated NK cells, CD8 T cells, and activated memory CD4 T cells. BMX showed positive correlations with eosinophils, mast cells, and neutrophils, while GRB10 was linked to eosinophils and M2 macrophages. Additionally, we constructed a comprehensive mRNA-miRNA-lncRNA regulatory network, identifying key interactions that may drive sepsis pathogenesis. Molecular docking and dynamics simulations validated Bendroflumethiazide, Cianidanol, and Hexamidine as promising therapeutic agents targeting these biomarkers. In conclusion, this integrated approach provides profound insights into the molecular mechanisms underlying sepsis, pinpointing BMX, GRB10, and GADD45A as pivotal biomarkers and therapeutic targets. These findings significantly enhance our understanding of sepsis pathophysiology and lay the groundwork for developing personalized diagnostic and therapeutic strategies aimed at improving patient outcomes.
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To identify gene modules associated with sepsis, we performed weighted gene co-expression network analysis (WGCNA) using the “WGCNA” package in R (Langfelder and Horvath, 2008).
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To identify gene modules associated with sepsis, we performed weighted gene co-expression network analysis (WGCNA) using the “WGCNA” package in R (Langfelder and Horvath, 2008).
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Publicly available datasets were analyzed in this study. These data can be found here: https://www.ncbi.nlm.nih.gov/geo/, using accession numbers GSE28750, GSE26440, GSE13205, and GSE9960.
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Analysis of four GEO microarray datasets using transcriptomics and machine learning identified BMX, GRB10, and GADD45A as pivotal sepsis biomarkers with diagnostic AUC values above 0.9.
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Analyzing microarray data from the Gene Expression Omnibus (GEO) datasets GSE28750, GSE26440, GSE13205, and GSE9960, we discovered three pivotal biomarkers that BMX (bone marrow tyrosine kinase gene on chromosome X), GRB10 (growth factor receptor bound protein 10), and GADD45A (growth arrest and DNA damage inducible alpha), exhibiting exceptional diagnostic accuracy (AUC >0.9).
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Analysis of four GEO microarray datasets using transcriptomics and machine learning identified BMX, GRB10, and GADD45A as pivotal sepsis biomarkers with diagnostic AUC values above 0.9.
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Publicly available datasets were analyzed in this study. These data can be found here: https://www.ncbi.nlm.nih.gov/geo/, using accession numbers GSE28750, GSE26440, GSE13205, and GSE9960.
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The paper names GSE28750, GSE26440, GSE13205, GSE9960 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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and therapeutic targets in sepsis. Analyzing microarray data from the Gene Expression Omnibus (GEO)
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okine signaling for GRB10, and regulation of apoptosis for GADD45A (Figures 4G–I). These findings d
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40230692", "kind": "science-record", "revision": 3, "content_hash": "sha256:925a8805942dd5eaf9c5d87a63b70ab65f0846f9271d9bf4ebfe1db81a49843a", "created_at": "2026-11-01T20:30:23Z", "updated_at": "2026-11-01T22:13:53Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Machine learning-based transcriptmics analysis reveals BMX, GRB10, and GADD45A as crucial biomarkers and therapeutic targets in sepsis.", "doi": "10.3389/fphar.2025.1576467", "pmid": "40230692", "authors": ["Yanwei Cheng", "Haoran Peng", "Qiao Chen", "Lijun Xu", "Lijie Qin"], "journal": "Frontiers in pharmacology", "year": 2025, "abstract": "Sepsis is a life-threatening condition characterized by a dysregulated host response to infection, resulting in high mortality rates and complex clinical management. This study leverages transcriptomics and machine learning (ML) to identify critical biomarkers and therapeutic targets in sepsis. Analyzing microarray data from the Gene Expression Omnibus (GEO) datasets GSE28750, GSE26440, GSE13205, and GSE9960, we discovered three pivotal biomarkers that BMX (bone marrow tyrosine kinase gene on chromosome X), GRB10 (growth factor receptor bound protein 10), and GADD45A (growth arrest and DNA damage inducible alpha), exhibiting exceptional diagnostic accuracy (AUC >0.9). Functional enrichment analyses revealed that these genes play key roles in reactive oxygen species metabolism and immune response regulation. Specifically, GADD45A was positively correlated with eosinophils and inversely associated with activated NK cells, CD8 T cells, and activated memory CD4 T cells. BMX showed positive correlations with eosinophils, mast cells, and neutrophils, while GRB10 was linked to eosinophils and M2 macrophages. Additionally, we constructed a comprehensive mRNA-miRNA-lncRNA regulatory network, identifying key interactions that may drive sepsis pathogenesis. Molecular docking and dynamics simulations validated Bendroflumethiazide, Cianidanol, and Hexamidine as promising therapeutic agents targeting these biomarkers. In conclusion, this integrated approach provides profound insights into the molecular mechanisms underlying sepsis, pinpointing BMX, GRB10, and GADD45A as pivotal biomarkers and therapeutic targets. 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