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pmid:37252693

Integrated bioinformatics approach reveals methylation-regulated differentially expressed genes in obesity.

Guilherme Coutinho Kullmann Duarte · Felipe Pellenz · Daisy Crispim · Tais Silveira Assmann

Archives of endocrinology and metabolism · 2023 doi:10.20945/2359-3997000000604

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:37252693
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2026-11-01T19:01:58Z
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2026-11-01T22:09:35Z
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paper object · 10 fields
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title
Integrated bioinformatics approach reveals methylation-regulated differentially expressed genes in obesity.
doi
10.20945/2359-3997000000604
pmid
37252693
authors array · 4 items
[0]
Guilherme Coutinho Kullmann Duarte
[1]
Felipe Pellenz
[2]
Daisy Crispim
[3]
Tais Silveira Assmann
journal
Archives of endocrinology and metabolism
year
2023
abstract
Objective: To identify DNA methylation and gene expression profiles involved in obesity by implementing an integrated bioinformatics approach. Materials and methods: Gene expression (GSE94752, GSE55200, and GSE48964) and DNA methylation (GSE67024 and GSE111632) datasets were obtained from the GEO database. Differentially expressed genes (DEGs) and differentially methylated genes (DMGs) in subcutaneous adipose tissue of patients with obesity were identified using GEO2R. Methylation-regulated DEGs (MeDEGs) were identified by overlapping DEGs and DMGs. The protein-protein interaction (PPI) network was constructed with the STRING database and analyzed using Cytoscape. Functional modules and hub-bottleneck genes were identified by using MCODE and CytoHubba plugins. Functional enrichment analyses were performed based on Gene Ontology terms and KEGG pathways. To prioritize and identify candidate genes for obesity, MeDEGs were compared with obesity-related genes available at the DisGeNET database. Results: A total of 54 MeDEGs were identified after overlapping the lists of significant 274 DEGs and 11,556 DMGs. Of these, 25 were hypermethylated-low expression genes and 29 were hypomethylated-high expression genes. The PPI network showed three hub-bottleneck genes (PTGS2, TNFAIP3, and FBXL20) and one functional module. The 54 MeDEGs were mainly involved in the regulation of fibroblast growth factor production, the molecular function of arachidonic acid, and ubiquitin-protein transferase activity. Data collected from DisGeNET showed that 11 of the 54 MeDEGs were involved in obesity. Conclusion: This study identifies new MeDEGs involved in obesity and assessed their related pathways and functions. These results data may provide a deeper understanding of methylation-mediated regulatory mechanisms of obesity.
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DEGs were defined based on an absolute log2-Fold Change (log FC) > 2.0 and P < 0.05. To identify DMGs, |t|>2 and P < 0.05 were used as cutoff points.
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sections[4] "Data processing" paragraph 3
quote
DEGs were defined based on an absolute log2-Fold Change (log FC) > 2.0 and P < 0.05. To identify DMGs, |t|>2 and P < 0.05 were used as cutoff points.
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Ethical approval: this study used anonymized publicly available data, including GSE94752, GSE55200, GSE48964, GSE67024, and GSE111632 (further information on the approval by the Research Ethics Committees is available at: https://www.ncbi.nlm.nih.gov/geo/ ).
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sections[16] "Footnotes" paragraph 2
quote
Ethical approval: this study used anonymized publicly available data, including GSE94752, GSE55200, GSE48964, GSE67024, and GSE111632 (further information on the approval by the Research Ethics Committees is available at: https://www.ncbi.nlm.nih.gov/geo/ ).
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The study identified 54 methylation-regulated differentially expressed genes in obesity, including 25 hypermethylated-low-expression genes and 29 hypomethylated-high-expression genes.
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A total of 54 MeDEGs were identified after overlapping the lists of significant 274 DEGs and 11,556 DMGs. Of these, 25 were hypermethylated-low expression genes and 29 were hypomethylated-high expression genes.
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The study identified 54 methylation-regulated differentially expressed genes in obesity, including 25 hypermethylated-low-expression genes and 29 hypomethylated-high-expression genes.
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[2] object · 3 fields
id
data:geo:GSE111632
type
dataset
label
GEO GSE111632
agent
agent:corpus-assay-engine
[1] object · 4 fields
id
activity-read-37252693
type
extraction
used array · 1 item
[0]
source:pmid:37252693
agent
agent:minimax-reader
[2] object · 4 fields
id
activity-resolve-GSE111632
type
accession_resolution
used array · 1 item
[0]
data:geo:GSE111632
agent
agent:corpus-assay-engine
agents array · 2 items
[0] object · 3 fields
id
agent:corpus-assay-engine
type
software
label
Corpus assay engine
[1] object · 3 fields
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 object · 4 fields
parent_id
pmid:37252693
parent_hash
sha256:f03ad1ea4684d426cc1f68e59a32f5829d8550852975420228a1a313c5bbb0a7
fork_of
null
gaps array · 15 items
[0]
asset:data:geo:GSE111632 licence not read
[1]
asset:data:geo:GSE111632 not downloaded
[2]
asset:data:geo:GSE48964 licence not read
[3]
asset:data:geo:GSE48964 not downloaded
[4]
asset:data:geo:GSE55200 licence not read
[5]
asset:data:geo:GSE55200 not downloaded
[6]
asset:data:geo:GSE67024 licence not read
[7]
asset:data:geo:GSE67024 not downloaded
[8]
asset:data:geo:GSE94752 licence not read
[9]
asset:data:geo:GSE94752 not downloaded
[10]
execution.not_run
[11]
method.reader_named_unmapped
[12]
review.human_critique
[13]
review.independent_reader
[14]
review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
network_analysis
definition_version
f2132e96ae6c7a4e
required_operations array · 3 items
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build_graph
[1]
centrality_scores
[2]
pathway_enrich
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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protein-protein interaction
order_basis
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id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37252693", "kind": "science-record", "revision": 3, "content_hash": "sha256:889080524661127f4c7f560078137d5b4fe3b84151909918b3c09bd7e650078d", "created_at": "2026-11-01T19:01:58Z", "updated_at": "2026-11-01T22:09:35Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrated bioinformatics approach reveals methylation-regulated differentially expressed genes in obesity.", "doi": "10.20945/2359-3997000000604", "pmid": "37252693", "authors": ["Guilherme Coutinho Kullmann Duarte", "Felipe Pellenz", "Daisy Crispim", "Tais Silveira Assmann"], "journal": "Archives of endocrinology and metabolism", "year": 2023, "abstract": "Objective: To identify DNA methylation and gene expression profiles involved in obesity by implementing an integrated bioinformatics approach.\nMaterials and methods: Gene expression (GSE94752, GSE55200, and GSE48964) and DNA methylation (GSE67024 and GSE111632) datasets were obtained from the GEO database. Differentially expressed genes (DEGs) and differentially methylated genes (DMGs) in subcutaneous adipose tissue of patients with obesity were identified using GEO2R. Methylation-regulated DEGs (MeDEGs) were identified by overlapping DEGs and DMGs. The protein-protein interaction (PPI) network was constructed with the STRING database and analyzed using Cytoscape. Functional modules and hub-bottleneck genes were identified by using MCODE and CytoHubba plugins. Functional enrichment analyses were performed based on Gene Ontology terms and KEGG pathways. To prioritize and identify candidate genes for obesity, MeDEGs were compared with obesity-related genes available at the DisGeNET database.\nResults: A total of 54 MeDEGs were identified after overlapping the lists of significant 274 DEGs and 11,556 DMGs. Of these, 25 were hypermethylated-low expression genes and 29 were hypomethylated-high expression genes. The PPI network showed three hub-bottleneck genes (PTGS2, TNFAIP3, and FBXL20) and one functional module. The 54 MeDEGs were mainly involved in the regulation of fibroblast growth factor production, the molecular function of arachidonic acid, and ubiquitin-protein transferase activity. Data collected from DisGeNET showed that 11 of the 54 MeDEGs were involved in obesity.\nConclusion: This study identifies new MeDEGs involved in obesity and assessed their related pathways and functions. These results data may provide a deeper understanding of methylation-mediated regulatory mechanisms of obesity.", "claims": [{"id": "claim-method", "statement": "DEGs were defined based on an absolute log2-Fold Change (log FC) > 2.0 and P < 0.05. To identify DMGs, |t|>2 and P < 0.05 were used as cutoff points.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37252693", "locator": "sections[4] \"Data processing\" paragraph 3", "quote": "DEGs were defined based on an absolute log2-Fold Change (log FC) > 2.0 and P < 0.05. To identify DMGs, |t|>2 and P < 0.05 were used as cutoff points."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Ethical approval: this study used anonymized publicly available data, including GSE94752, GSE55200, GSE48964, GSE67024, and GSE111632 (further information on the approval by the Research Ethics Committees is available at: https://www.ncbi.nlm.nih.gov/geo/ ).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37252693", "locator": "sections[16] \"Footnotes\" paragraph 2", "quote": "Ethical approval: this study used anonymized publicly available data, including GSE94752, GSE55200, GSE48964, GSE67024, and GSE111632 (further information on the approval by the Research Ethics Committees is available at: https://www.ncbi.nlm.nih.gov/geo/ )."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified 54 methylation-regulated differentially expressed genes in obesity, including 25 hypermethylated-low-expression genes and 29 hypomethylated-high-expression genes.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37252693", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "A total of 54 MeDEGs were identified after overlapping the lists of significant 274 DEGs and 11,556 DMGs. Of these, 25 were hypermethylated-low expression genes and 29 were hypomethylated-high expression genes."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified 54 methylation-regulated differentially expressed genes in obesity, including 25 hypermethylated-low-expression genes and 29 hypomethylated-high-expression genes.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:37252693"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE111632"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE111632"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37252693", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.20945/2359-3997000000604", "sha256": 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GSE111632 (further information on the approval by the Research Ethics Committees is available at: https://www.ncbi.nlm.nih.gov/geo/ ).", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "Ethical approval: this study used anonymized publicly available data, including GSE94752, GSE55200, GSE48964, GSE67024, and GSE111632 (further information on the approval by the Research Ethics Committees is available at: https://www.ncbi.nlm.nih.gov/geo/ ).", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM3035977", "GSM3035978", "GSM3035979", "GSM3035980", "GSM3035981", "GSM3035982", "GSM3035983", "GSM3035984", "GSM3035985", "GSM3035986", "GSM3035987", "GSM3035988"], "sample_count": 12, "group_sizes": null, "group_sizes_basis": null, "platform": "13534", "taxon": "Homo sapiens", "title": "Adipose derived stem cells (ASCs) methylation differences between lean and obese individuals", "resolution_checked_at": 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