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pmid:39546499

Exploration of a miRNA-mRNA network shared between acute pancreatitis and Epstein-Barr virus infection by integrated bioinformatics analysis.

Xing Wei · Zhen Weng · Xia Xu · Jian Yao

PloS one · 2024 doi:10.1371/journal.pone.0311130

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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title
Exploration of a miRNA-mRNA network shared between acute pancreatitis and Epstein-Barr virus infection by integrated bioinformatics analysis.
doi
10.1371/journal.pone.0311130
pmid
39546499
authors array · 4 items
[0]
Xing Wei
[1]
Zhen Weng
[2]
Xia Xu
[3]
Jian Yao
journal
PloS one
year
2024
abstract
Acute pancreatitis (AP) stands out as a primary cause of hospitalization within gastrointestinal ailments, attributed to diverse factors, including Epstein-Barr virus (EBV) infection. Nevertheless, the common miRNAs and genes shared between AP and EBV infection remain unclear. In the present study, four datasets GSE194331, GSE42455, GSE45918 and GSE109220 were selected and downloaded from the Gene Expression Omnibus (GEO) database. Differential expression analysis was performed to screen for differentially expressed genes (DEGs) and differentially expressed miRNAs (DEMs). Target genes of overlapping DEMs were predicted, and intersections with overlapping DEGs were used to construct a miRNA-mRNA network. In addition, the enrichment analysis, drug prediction, diagnostic accuracy assessment, competitive endogenous RNA (ceRNA) network construction, transcription factor (TF)-miRNA-mRNA network construction, and immune cell infiltration analysis were also carried out. We found a total of 111 genes and 8 miRNAs shared between AP and EBV infection. A miRNA-mRNA network was constructed, which comprised 5 miRNAs and 10 genes exhibiting robust diagnostic performance. Histone deacetylase (HDAC) inhibitor was identified as a novel therapeutic intervention from drug prediction analysis. The results of immune cell infiltration analysis revealed that a consistent and significant difference could be found on activated B cell in AP and EBV-infected individuals in comparison to the controls. Taken together, our work, for the first time, revealed a miRNA-mRNA network shared between AP and EBV infection, thereby enriching a deeper comprehension of the intricate molecular mechanisms and potential therapeutic targets entwined in these two pathological conditions.
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Finally, the DESeq2 (version 1.44.0) package [22], which provides methods to test for differential expression by use of negative binomial generalized linear models on un-normalized RNA-seq counts data, was employed to identify the DEGs between 76 AP patients and 32 healthy controls in the dataset GSE194331. The limma is an R package for the analysis of gene expression data, especially the use of linear models for assessment of differential expression on normalized microarray data, which was used to identify the DEGs across 8 samples before and after acquisition of EBV infection in the dataset GSE45918. Similarly, in the dataset GSE109220, the limma package was used to identify the DEMs between 5 infectious mononucleosis diagnosis samples and 3 healthy controls. Within the dataset GSE42455, the limma package was employed for DEMs identification between 10 AP rat models and 5 sham samples.
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sections[5] "Differential expression analysis" paragraph 2
quote
Finally, the DESeq2 (version 1.44.0) package [22], which provides methods to test for differential expression by use of negative binomial generalized linear models on un-normalized RNA-seq counts data, was employed to identify the DEGs between 76 AP patients and 32 healthy controls in the dataset GSE194331. The limma is an R package for the analysis of gene expression data, especially the use of linear models for assessment of differential expression on normalized microarray data, which was used to identify the DEGs across 8 samples before and after acquisition of EBV infection in the dataset GSE45918. Similarly, in the dataset GSE109220, the limma package was used to identify the DEMs between 5 infectious mononucleosis diagnosis samples and 3 healthy controls. Within the dataset GSE42455, the limma package was employed for DEMs identification between 10 AP rat models and 5 sham samples.
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All datasets are available from the GEO database (GSE194331, GSE42455, GSE45918 and GSE109220). All relevant data are within the paper and its supporting information files.
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The study identified a shared miRNA-mRNA network between acute pancreatitis and Epstein-Barr virus infection comprising 5 miRNAs and 10 genes.
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A miRNA-mRNA network was constructed, which comprised 5 miRNAs and 10 genes exhibiting robust diagnostic performance.
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We found a total of 111 genes and 8 miRNAs shared between AP and EBV infection.
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The study identified a shared miRNA-mRNA network between acute pancreatitis and Epstein-Barr virus infection comprising 5 miRNAs and 10 genes.
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miRNA expression data from human PBMC derived form acute infectious mononucleosis patients
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Gene Expression Profiling of Acute Pancreatitis
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microRNA expression in Mestenteric lymph samples from rat models of acute pancreatitis
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Finally, the DESeq2 (version 1.44.0) package [22], which provides methods to test for differential expression by use of negative binomial generalized linear models on un-normalized RNA-seq counts data, was employed to identify the DEGs between 76 AP patients and 32 healthy controls in the dataset GSE194331. The limma is an R package for the analysis of gene expression data, especially the use of linear models for assessment of differential expression on normalized microarray data, which was used to identify the DEGs across 8 samples before and after acquisition of EBV infection in the dataset GSE45918. Similarly, in the dataset GSE109220, the limma package was used to identify the DEMs between 5 infectious mononucleosis diagnosis samples and 3 healthy controls. Within the dataset GSE42455, the limma package was employed for DEMs identification between 10 AP rat models and 5 sham samples.
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Finally, the DESeq2 (version 1.44.0) package [22], which provides methods to test for differential expression by use of negative binomial generalized linear models on un-normalized RNA-seq counts data, was employed to identify the DEGs between 76 AP patients and 32 healthy controls in the dataset GSE194331. The limma is an R package for the analysis of gene expression data, especially the use of linear models for assessment of differential expression on normalized microarray data, which was used to identify the DEGs across 8 samples before and after acquisition of EBV infection in the dataset GSE45918. Similarly, in the dataset GSE109220, the limma package was used to identify the DEMs between 5 infectious mononucleosis diagnosis samples and 3 healthy controls. Within the dataset GSE42455, the limma package was employed for DEMs identification between 10 AP rat models and 5 sham samples.
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Complete file
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Nevertheless, the common miRNAs and genes shared between AP and EBV infection remain unclear. In the present study, four datasets GSE194331, GSE42455, GSE45918 and GSE109220 were selected and downloaded from the Gene Expression Omnibus (GEO) database. Differential expression analysis was performed to screen for differentially expressed genes (DEGs) and differentially expressed miRNAs (DEMs). Target genes of overlapping DEMs were predicted, and intersections with overlapping DEGs were used to construct a miRNA-mRNA network. In addition, the enrichment analysis, drug prediction, diagnostic accuracy assessment, competitive endogenous RNA (ceRNA) network construction, transcription factor (TF)-miRNA-mRNA network construction, and immune cell infiltration analysis were also carried out. We found a total of 111 genes and 8 miRNAs shared between AP and EBV infection. A miRNA-mRNA network was constructed, which comprised 5 miRNAs and 10 genes exhibiting robust diagnostic performance. Histone deacetylase (HDAC) inhibitor was identified as a novel therapeutic intervention from drug prediction analysis. The results of immune cell infiltration analysis revealed that a consistent and significant difference could be found on activated B cell in AP and EBV-infected individuals in comparison to the controls. Taken together, our work, for the first time, revealed a miRNA-mRNA network shared between AP and EBV infection, thereby enriching a deeper comprehension of the intricate molecular mechanisms and potential therapeutic targets entwined in these two pathological conditions.", "claims": [{"id": "claim-method", "statement": "Finally, the DESeq2 (version 1.44.0) package [22], which provides methods to test for differential expression by use of negative binomial generalized linear models on un-normalized RNA-seq counts data, was employed to identify the DEGs between 76 AP patients and 32 healthy controls in the dataset GSE194331. 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Within the dataset GSE42455, the limma package was employed for DEMs identification between 10 AP rat models and 5 sham samples."}}, {"id": "method-2", "family": "differential_expression", "specific": "limma_voom", "label": "Differential expression analysis", "dsl_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["count_matrix_with_condition"], "evidence": {"score": 0.8, "band": "high", "quote": "limma"}}, {"id": "method-3", "family": "correlation_analysis", "specific": "pearson", "label": "Correlation analysis", "dsl_operations": ["pearson_r"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["paired_numeric_columns"], "evidence": {"score": 0.8, "band": "high", "quote": "Pearson correlation"}}], "targets": [], "gaps": []}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "complete", "tier": "R1", "blocking_axis": "none", "blocked_on": "nothing:replicable_now", "axes": {"method": {"tier": "R1", "expressible": true, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "missing_operations": [], "basis": "The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: deseq2."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R1", "reachable": true, "accessions": ["GSE194331", "GSE45918", "GSE42455", "GSE109220"], "resolved_accessions": ["GSE194331", "GSE45918", "GSE42455", "GSE109220"], "statements": ["All datasets are available from the GEO database (GSE194331, GSE42455, GSE45918 and GSE109220). All relevant data are within the paper and its supporting information files."], "basis": "The paper names GSE194331, GSE45918, GSE42455, GSE109220 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "assets": ["source:pmid:39546499", "data:geo:GSE109220"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:GSE109220"]}, "gaps": []}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-11-01T19:38:35Z", "independence": "single_reader"}, "evidence_check": {"method": "verbatim", "availability": "verbatim"}, "calls": 5, "usage": {"prompt_tokens": 20771, "completion_tokens": 1401, "cached_tokens": 256}}, "human_critique": null, "stages": [{"id": "extraction", "state": "complete", "reader": "MiniMax-M3.1-Flash", "provider": "minimax"}], "gaps": ["review.independent_reader", "review.machine_critique", "review.human_critique"]}, "execution": {"state": "absent", "status": "not_run", "mode": null, "runs": [], "gaps": ["execution.not_run"]}, "provenance": {"entities": [{"id": "pmid:39546499", "type": "paper", "label": "pmid:39546499"}, {"id": "source:pmid:39546499", "type": "manuscript", "label": "PMID 39546499 full text"}, {"id": "data:geo:GSE109220", "type": "dataset", "label": "GEO GSE109220"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:39546499", "type": "paper", "label": "pmid:39546499"}, {"id": "source:pmid:39546499", "type": "manuscript", "label": "PMID 39546499 full text"}, {"id": "data:geo:GSE109220", "type": "dataset", "label": "GEO GSE109220"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-39546499", "type": "extraction", "used": ["source:pmid:39546499"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-GSE109220", "type": "accession_resolution", "used": ["data:geo:GSE109220"], "agent": "agent:corpus-assay-engine"}], "agents": [{"id": "agent:corpus-assay-engine", "type": "software", "label": "Corpus assay engine"}, {"id": "agent:minimax-reader", "type": "software", "label": "MiniMax literature reader"}], "source_run_id": "reading-sci-2026-11-01", "dsl_catalogue_fingerprint": "343fb30756ba6ec3", "capability_table_fingerprint": "2cb3e42f047d2ecf", "snapshot_id": "ba34b49490d9bfaf"}, "lineage": {"parent_id": "pmid:39546499", "parent_hash": "sha256:dc7bffd68b1f3638934caffa4af3c1ec37577629b67bc505131042e99e3fb675", "fork_of": null, "generation": 3}, "gaps": ["asset:data:geo:GSE109220 licence not read", "asset:data:geo:GSE109220 not downloaded", "asset:data:geo:GSE194331 licence not read", "asset:data:geo:GSE194331 not downloaded", "asset:data:geo:GSE42455 licence not read", "asset:data:geo:GSE42455 not downloaded", "asset:data:geo:GSE45918 licence not read", "asset:data:geo:GSE45918 not downloaded", "execution.not_run", "review.human_critique", "review.independent_reader", "review.machine_critique"], "assays": [{"role": "analysis", "definition_id": "differential_expression", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "support_state": "supported", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["Finally, the DESeq2 (version 1.44.0) package [22], which provides methods to test for differential expression by use of negative binomial generalized linear models on un-normalized RNA-seq counts data, was employed to identify the DEGs between 76 AP patients and 32 healthy controls in the dataset GSE194331. The limma is an R package for the analysis of gene expression data, especially the use of linear models for assessment of differential expression on normalized microarray data, which was used to identify the DEGs across 8 samples before and after acquisition of EBV infection in the dataset GSE45918. Similarly, in the dataset GSE109220, the limma package was used to identify the DEMs between 5 infectious mononucleosis diagnosis samples and 3 healthy controls. Within the dataset GSE42455, the limma package was employed for DEMs identification between 10 AP rat models and 5 sham samples."], "order_basis": "analysis_only", "id": "assay:1"}]}