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pmid:40328806

Integrated bioinformatics, machine learning, and molecular docking reveal crosstalk genes and potential drugs between periodontitis and systemic lupus erythematosus.

Junjie Wang · Qingao Deng · Lu Qi

Scientific reports · 2025 doi:10.1038/s41598-025-00620-3

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Experiment

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Data

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Analysis

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Integrated bioinformatics, machine learning, and molecular docking reveal crosstalk genes and potential drugs between periodontitis and systemic lupus erythematosus.
doi
10.1038/s41598-025-00620-3
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Junjie Wang
[1]
Qingao Deng
[2]
Lu Qi
journal
Scientific reports
year
2025
abstract
Evidence indicates a connection between periodontitis (PD) and systemic lupus erythematosus (SLE), though the underlying co-morbid mechanisms remain unclear. This study sought to identify the genetic factors and potential therapeutic agents involved in the interaction between PD and SLE. We employed multi-omics methodologies, encompassing differential expression analysis, weighted gene co-expression network analysis (WGCNA), functional enrichment (GO/KEGG), LASSO regression, diagnostic model construction, protein-protein interaction (PPI) networks, immune infiltration profiling, computational drug prediction, molecular docking, and disease subtyping, to analyze PD and SLE expression datasets from the Gene Expression Omnibus (GEO) database (GSE10334, GSE16134, GSE50772, and GSE81622). Cross-analysis identified 32 crosstalk genes (CGs) common to both PD and SLE. LASSO analysis pinpointed three key diagnostic genes (TAGLN, MMP9, TNFAIP6) for both conditions. The resulting diagnostic models demonstrated robust efficacy in both training and validation datasets. Four topological algorithms in Cytoscape highlighted four central crosstalk genes (TAGLN, MMP9, TNFAIP6, IL1B). Additionally, hesperidin, doxycycline, and cytochalasin D emerged as potential therapeutic agents. Two subtypes (C1 and C2) of PD and SLE were delineated based on CG expression profiles. The development of diagnostic models, potential drug identification, and disease subtype classification are poised to enhance diagnosis and treatment. These findings aim to deepen the understanding of PD and SLE complexities.
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To identify shared diagnostic genes for PD and SLE, we analyzed the CG matrices from GSE10334 and GSE50772 using the LASSO regression algorithm.
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To identify shared diagnostic genes for PD and SLE, we analyzed the CG matrices from GSE10334 and GSE50772 using the LASSO regression algorithm.
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The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/repository. The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
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Cross-analysis identified 32 crosstalk genes (CGs) common to both PD and SLE.
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Cross-analysis identified 32 crosstalk genes (CGs) common to both PD and SLE.
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Cross-analysis identified 32 crosstalk genes (CGs) common to both PD and SLE.
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[292]
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GSM404314
sample_count
310
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null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Bacterial Correlates of Gingival Gene Expression
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[3] object · 15 fields
id
data:geo:GSE50772
role
raw
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geo-series
media_type
application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE50772
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null
bytes
null
access
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resolved
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null
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reader_required
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GSE50772
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null
note
The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/repository. The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
structure object · 15 fields
repository
GEO
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GEO accession URL
access_statement_verbatim
The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/repository. The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
access_statement_kind
data_availability_statement
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sample_count
81
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null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Expression data in PBMCs from SLE patients and controls
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[4] object · 15 fields
id
data:geo:GSE81622
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raw
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geo-series
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application/vnd.ncbi.geo-series+json
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE81622
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null
bytes
null
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null
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null
note
The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/repository. The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
structure object · 15 fields
repository
GEO
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GEO accession URL
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The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/repository. The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
access_statement_kind
data_availability_statement
sample_accessions array · 55 items
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sample_count
55
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null
group_sizes_basis
null
platform
10558
taxon
Homo sapiens
title
Whole genome transcription and DNA methylation analysis of peripheral blood mononuclear cells identified aberrant gene regulation pathways in systemic lupus erythematosus [expression]
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
false
gaps array · 8 items
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asset:data:geo:GSE10334 not downloaded
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[5]
asset:data:geo:GSE50772 licence not read
[6]
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[7]
asset:data:geo:GSE81622 licence not read
analysis object · 4 fields
state
partial
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[0] object · 10 fields
id
method-1
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network_analysis
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ppi_network
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Network / pathway analysis
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[0]
build_graph
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pathway_enrich
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edge_list
evidence object · 3 fields
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medium
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protein-protein interaction
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id
method-2
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null
specific
null
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LASSO regression analysis
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score
1
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To identify shared diagnostic genes for PD and SLE, we analyzed the CG matrices from GSE10334 and GSE50772 using the LASSO regression algorithm.
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gaps array · 1 item
[0]
method.reader_named_unmapped
capability object · 3 fields
state
complete
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capability_id
capability:computational_analysis
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meta_analysis
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[7]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
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R1
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nothing:replicable_now
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true
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: ppi_network.
capability object · 4 fields
tier
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capability:computational_analysis
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owned
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
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[0]
GSE10334
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GSE50772
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GSE81622
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[0]
GSE10334
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GSE16134
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GSE50772
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GSE81622
statements array · 1 item
[0]
The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/repository. The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
basis
The paper names GSE10334, GSE16134, GSE50772, GSE81622 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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source:pmid:40328806
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data:geo:GSE10334
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run_analysis
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data:geo:GSE10334
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review object · 5 fields
state
partial
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kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T19:51:55Z
independence
single_reader
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method
verbatim
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verbatim
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5
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10018
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256
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id
extraction
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MiniMax-M3.1-Flash
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review.human_critique
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execution.not_run
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pmid:40328806
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paper
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pmid:40328806
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source:pmid:40328806
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manuscript
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PMID 40328806 full text
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id
data:geo:GSE10334
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dataset
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GEO GSE10334
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[0] object · 4 fields
id
activity-reading-sci-2026-11-01
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classification
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[0] object · 3 fields
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pmid:40328806
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paper
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pmid:40328806
[1] object · 3 fields
id
source:pmid:40328806
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manuscript
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PMID 40328806 full text
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id
data:geo:GSE10334
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dataset
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GEO GSE10334
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agent:corpus-assay-engine
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extraction
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agent:minimax-reader
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activity-resolve-GSE10334
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accession_resolution
used array · 1 item
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data:geo:GSE10334
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agent:corpus-assay-engine
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agent:corpus-assay-engine
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agent:minimax-reader
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MiniMax literature reader
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343fb30756ba6ec3
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pmid:40328806
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[5]
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40328806", "kind": "science-record", "revision": 3, "content_hash": "sha256:5e3e7fd07e22c206b6593785ed463d8aec768d1e65b9ae63abe9cfe0b4f4a4de", "created_at": "2026-11-01T20:30:29Z", "updated_at": "2026-11-01T22:14:01Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrated bioinformatics, machine learning, and molecular docking reveal crosstalk genes and potential drugs between periodontitis and systemic lupus erythematosus.", "doi": "10.1038/s41598-025-00620-3", "pmid": "40328806", "authors": ["Junjie Wang", "Qingao Deng", "Lu Qi"], "journal": "Scientific reports", "year": 2025, "abstract": "Evidence indicates a connection between periodontitis (PD) and systemic lupus erythematosus (SLE), though the underlying co-morbid mechanisms remain unclear. This study sought to identify the genetic factors and potential therapeutic agents involved in the interaction between PD and SLE. We employed multi-omics methodologies, encompassing differential expression analysis, weighted gene co-expression network analysis (WGCNA), functional enrichment (GO/KEGG), LASSO regression, diagnostic model construction, protein-protein interaction (PPI) networks, immune infiltration profiling, computational drug prediction, molecular docking, and disease subtyping, to analyze PD and SLE expression datasets from the Gene Expression Omnibus (GEO) database (GSE10334, GSE16134, GSE50772, and GSE81622). Cross-analysis identified 32 crosstalk genes (CGs) common to both PD and SLE. LASSO analysis pinpointed three key diagnostic genes (TAGLN, MMP9, TNFAIP6) for both conditions. The resulting diagnostic models demonstrated robust efficacy in both training and validation datasets. Four topological algorithms in Cytoscape highlighted four central crosstalk genes (TAGLN, MMP9, TNFAIP6, IL1B). Additionally, hesperidin, doxycycline, and cytochalasin D emerged as potential therapeutic agents. Two subtypes (C1 and C2) of PD and SLE were delineated based on CG expression profiles. The development of diagnostic models, potential drug identification, and disease subtype classification are poised to enhance diagnosis and treatment. These findings aim to deepen the understanding of PD and SLE complexities.", "claims": [{"id": "claim-method", "statement": "To identify shared diagnostic genes for PD and SLE, we analyzed the CG matrices from GSE10334 and GSE50772 using the LASSO regression algorithm.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40328806", "locator": "sections[17] \"Selection of shared diagnostic genes by LASSO analysis\" paragraph 2", "quote": "To identify shared diagnostic genes for PD and SLE, we analyzed the CG matrices from GSE10334 and GSE50772 using the LASSO regression algorithm."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets generated and/or analysed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/repository. 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