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pmid:40649881

Identification of Key Genes for Alcoholic Hepatitis Using Integrated Network Analysis of Differential lncRNA and Gene Expression.

Bihuan Hu · Hui Xia · Peixuan Tian · Xinbao Li · Yu Yang · Zixuan Zhu · Yajie Zhou · Wang Liao · Shoakang Wang · Ligang Yang · Guiju Sun · Jing Sui

International journal of molecular sciences · 2025 doi:10.3390/ijms26136104

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:40649881
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2026-11-01T20:30:44Z
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paper object · 10 fields
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title
Identification of Key Genes for Alcoholic Hepatitis Using Integrated Network Analysis of Differential lncRNA and Gene Expression.
doi
10.3390/ijms26136104
pmid
40649881
authors array · 12 items
[0]
Bihuan Hu
[1]
Hui Xia
[2]
Peixuan Tian
[3]
Xinbao Li
[4]
Yu Yang
[5]
Zixuan Zhu
[6]
Yajie Zhou
[7]
Wang Liao
[8]
Shoakang Wang
[9]
Ligang Yang
[10]
Guiju Sun
[11]
Jing Sui
journal
International journal of molecular sciences
year
2025
abstract
Alcoholic liver disease (ALD) is a type of liver disease with complex pathogenic factors. In 2019, alcohol caused 11 million life-years to be lost globally, and the mortality rate has continued to rise. This study aims to explore the exclusive gene profile of AH and construct an mRNA-lncRNA regulatory network through an integrative analysis and database validation to reveal potential key biomarkers. We obtained expression data for alcoholic hepatitis from the GEO database; screened differentially expressed genes (DEGs) through a weighted gene co-expression network analysis (WGCNA); conducted a GO&KEGG analysis; and focused on the enrichment pathways for the top 20 genes. Hub genes were selected using cytoHubba and MCODE to construct the mRNA-lncRNA regulatory network, and key genes were confirmed using GSE167308 and GSE28619. We obtained 2552 differentially expressed mRNAs and 555 differentially expressed lncRNAs from three databases. Differentially expressed genes are mainly involved in pathways such as lipid metabolism disorders, complement activation, the activation of cancer-related pathways, the excessive activation of inflammatory immunity, and the initiation of cell adhesion and fibrosis. Based on the hub gene analysis, we screened out 43 key genes. By constructing the key mRNA-lncRNA-pathway network, we identified 12 mRNAs (AQP1, ELOVL7, ITPR3, KRT19, KRT23, LAMC2, MMP7, PROM1, SPINT1, STK39, TNFRSF21, and VTCN1) and 14 lncRNAs that play an important role in the occurrence and development of alcoholic hepatitis. To sum up, this article mainly expounds upon the key genes in the occurrence and development of alcoholic hepatitis. The key genes are mainly concentrated within signaling pathways such as metabolic pathways, fatty acid metabolism, and cancer pathways. Twelve differentially expressed mRNAs in the co-expression network can be used as biomarkers and intervention targets for the diagnosis and treatment of alcoholic hepatitis.
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Standardized datasets were statistically compared using Student’s t test or a one-way ANOVA. p < 0.05 was considered significant.
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Data Availability StatementThe original data presented in the study are openly available in GEO datasets at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143318; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE142530; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155907; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE28619; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE167308 (accessed on 19 June 2025).
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Data Availability StatementThe original data presented in the study are openly available in GEO datasets at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143318; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE142530; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155907; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE28619; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE167308 (accessed on 19 June 2025).
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Twelve differentially expressed mRNAs in the co-expression network can be used as biomarkers and intervention targets for the diagnosis and treatment of alcoholic hepatitis.
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Twelve differentially expressed mRNAs in the co-expression network can be used as biomarkers and intervention targets for the diagnosis and treatment of alcoholic hepatitis.
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Twelve differentially expressed mRNAs in the co-expression network can be used as biomarkers and intervention targets for the diagnosis and treatment of alcoholic hepatitis.
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Data Availability StatementThe original data presented in the study are openly available in GEO datasets at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143318; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE142530; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155907; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE28619; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE167308 (accessed on 19 June 2025).
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Data Availability StatementThe original data presented in the study are openly available in GEO datasets at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143318; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE142530; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155907; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE28619; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE167308 (accessed on 19 June 2025).
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Integrated Multi-Omics Analysis Reveals Glucose Metabolic Reprogramming and Identifies a Novel Hexokinase in Alcoholic Hepatitis
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RNAseq analysis highlights significant transcriptional changes within the livers of patients with alcoholic hepatitis.
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Data Availability StatementThe original data presented in the study are openly available in GEO datasets at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143318; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE142530; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155907; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE28619; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE167308 (accessed on 19 June 2025).
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Pathogenesis of alcoholic hepatitis
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Data Availability StatementThe original data presented in the study are openly available in GEO datasets at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143318; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE142530; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155907; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE28619; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE167308 (accessed on 19 June 2025).
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Transcriptome Analysis Identifies Fn14, a TNF Superfamily Receptor Member, as a Therapeutic Target in Alcoholic Hepatitis
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2026-11-01T15:39:54Z
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Data Availability StatementThe original data presented in the study are openly available in GEO datasets at https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143318; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE142530; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE155907; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE28619; https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE167308 (accessed on 19 June 2025).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40649881", "kind": "science-record", "revision": 4, "content_hash": "sha256:20351afc5a30a5f141b84624cac12c7f795ceea75d455373b3f5e8eaa466a5f6", "created_at": "2026-11-01T20:30:44Z", "updated_at": "2026-11-01T22:56:49Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of Key Genes for Alcoholic Hepatitis Using Integrated Network Analysis of Differential lncRNA and Gene Expression.", "doi": "10.3390/ijms26136104", "pmid": "40649881", "authors": ["Bihuan Hu", "Hui Xia", "Peixuan Tian", "Xinbao Li", "Yu Yang", "Zixuan Zhu", "Yajie Zhou", "Wang Liao", "Shoakang Wang", "Ligang Yang", "Guiju Sun", "Jing Sui"], "journal": "International journal of molecular sciences", "year": 2025, "abstract": "Alcoholic liver disease (ALD) is a type of liver disease with complex pathogenic factors. In 2019, alcohol caused 11 million life-years to be lost globally, and the mortality rate has continued to rise. This study aims to explore the exclusive gene profile of AH and construct an mRNA-lncRNA regulatory network through an integrative analysis and database validation to reveal potential key biomarkers. We obtained expression data for alcoholic hepatitis from the GEO database; screened differentially expressed genes (DEGs) through a weighted gene co-expression network analysis (WGCNA); conducted a GO&KEGG analysis; and focused on the enrichment pathways for the top 20 genes. Hub genes were selected using cytoHubba and MCODE to construct the mRNA-lncRNA regulatory network, and key genes were confirmed using GSE167308 and GSE28619. We obtained 2552 differentially expressed mRNAs and 555 differentially expressed lncRNAs from three databases. Differentially expressed genes are mainly involved in pathways such as lipid metabolism disorders, complement activation, the activation of cancer-related pathways, the excessive activation of inflammatory immunity, and the initiation of cell adhesion and fibrosis. Based on the hub gene analysis, we screened out 43 key genes. By constructing the key mRNA-lncRNA-pathway network, we identified 12 mRNAs (AQP1, ELOVL7, ITPR3, KRT19, KRT23, LAMC2, MMP7, PROM1, SPINT1, STK39, TNFRSF21, and VTCN1) and 14 lncRNAs that play an important role in the occurrence and development of alcoholic hepatitis. To sum up, this article mainly expounds upon the key genes in the occurrence and development of alcoholic hepatitis. The key genes are mainly concentrated within signaling pathways such as metabolic pathways, fatty acid metabolism, and cancer pathways. Twelve differentially expressed mRNAs in the co-expression network can be used as biomarkers and intervention targets for the diagnosis and treatment of alcoholic hepatitis.", "claims": [{"id": "claim-method", "statement": "Standardized datasets were statistically compared using Student’s t test or a one-way ANOVA. p < 0.05 was considered significant.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40649881", "locator": "sections[17] \"4.7. 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