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pmid:41583468

The role of 5-methylcytosine regulator-related genes in diagnostic and immune regulatory functions in atherosclerosis.

Hui Zhao · Ying Kong · Pengfei Ding · Luqun Yang · Ning Li

Frontiers in immunology · 2025 doi:10.3389/fimmu.2025.1636323

Paper

complete

Experiment

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Data

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Analysis

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Execution

absent

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title
The role of 5-methylcytosine regulator-related genes in diagnostic and immune regulatory functions in atherosclerosis.
doi
10.3389/fimmu.2025.1636323
pmid
41583468
authors array · 5 items
[0]
Hui Zhao
[1]
Ying Kong
[2]
Pengfei Ding
[3]
Luqun Yang
[4]
Ning Li
journal
Frontiers in immunology
year
2025
abstract
Background: Atherosclerosis (AS) is a chronic inflammatory disease with a poor prognosis, and 5-methylcytosine (m5C) RNA modification plays a significant role in AS-induced cardio-cerebrovascular diseases (CCVDs). However, the effects of m5C modification and related genes in AS remain unclear. Methods: We analyzed the correlations between m5C RNA modification and its regulatory genes in AS using microarray databases. Specifically, microarray datasets of AS (GSE90074, GSE27034, GSE59421, and GSE159677) were obtained from the Gene Expression Omnibus (GEO) database. Following differential expression and Spearman correlation analyses using GSE90074, m5C regulator-related genes (MRRGs) were screened to construct a protein-protein interaction (PPI) network. A least absolute shrinkage and selection operator (LASSO) logistic regression model was constructed and validated using receiver operating characteristic (ROC) curves in GSE90074 and GSE27034 to identify feature genes. Consensus clustering analysis was then performed to classify AS samples into distinct clusters. In addition, Spearman correlation analysis was used to explore the associations between differentially expressed m5C regulators (DE-MRs) and immune cells based on the identified clusters. Weighted gene co-expression network analysis (WGCNA) was applied to identify AS-related module genes. Subsequently, intersecting genes common to module genes and differentially expressed genes (DEGs) across AS-related clusters were considered candidate biomarkers and were validated by quantitative real-time polymerase chain reaction (qRT-PCR) in human myeloid leukemia mononuclear cells (THP-1). Single-cell RNA sequencing (scRNA-seq) analysis was performed to characterize the immune microenvironment of AS. In vitro experiments and genetic interventions were conducted to investigate the effects of the m5C regulator NSUN3 on macrophage function. Finally, a competitive endogenous RNA (ceRNA) network targeting the identified biomarkers was predicted using the miRNet database. Results: Based on two differentially expressed m5C regulators (NSUN3 and NSUN5), 546 of 2247 DEGs between AS and control samples were identified as MRRGs for PPI network construction. Twenty hub MRRGs were further incorporated into the LASSO logistic regression model, yielding nine feature genes. Based on these feature genes, AS samples were classified into two clusters, with five immune cell types showing significant differences between clusters. Both NSUN3 and NSUN5 showed the strongest correlations with M0 macrophages. A total of 643 module genes were identified and overlapped with DEGs from the two AS-related clusters, resulting in five biomarkers-MCL1, F13A1, RGS2, Toll-like receptor 8 (TLR8), and TAGAP. The expression patterns of these five biomarkers in the foam cell model were consistent with those observed in public datasets. Furthermore, NSUN3 regulated the production of proinflammatory cytokines in macrophages. Finally, a ceRNA regulatory network was constructed. Conclusion: Five potential diagnostic biomarkers for AS-MCL1, F13A1, RGS2, TLR8, and TAGAP-were identified. In addition, the m5C regulator NSUN3 plays a critical role in macrophage function, providing experimental evidence that may support the diagnosis and treatment of AS.
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Correlations between DEGs and DE-MRs were calculated using Spearman correlation analysis with |Cor| > 0.3 and p < 0.05 to screen for m5C regulator-related genes (MRRGs).
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Correlations between DEGs and DE-MRs were calculated using Spearman correlation analysis with |Cor| > 0.3 and p < 0.05 to screen for m5C regulator-related genes (MRRGs).
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Five potential diagnostic biomarkers for AS—MCL1, F13A1, RGS2, TLR8, and TAGAP—were identified.
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Five potential diagnostic biomarkers for AS—MCL1, F13A1, RGS2, TLR8, and TAGAP—were identified.
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Five potential diagnostic biomarkers for AS—MCL1, F13A1, RGS2, TLR8, and TAGAP—were identified.
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count_matrix_with_condition
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regression_modelling
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glm_logit_fit
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data_shapes array · 1 item
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evidence object · 3 fields
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hierarchical_cluster
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data_shapes array · 1 item
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feature_matrix
evidence object · 3 fields
score
0.8
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network_analysis
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Network / pathway analysis
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build_graph
[1]
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pathway_enrich
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evidence object · 3 fields
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0.7
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method-7
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network_analysis
specific
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label
Network / pathway analysis
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pathway_enrich
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evidence object · 3 fields
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method.reader_differs_from_extractor
capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
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[0]
meta_analysis
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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blocked_on
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required_operations array · 1 item
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spearman_rho
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: spearman.
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capability:computational_analysis
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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
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[0]
GSE90074
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GSE27034
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GSE159677
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GSE90074
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GSE27034
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GSE159677
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GSE59421
statements array · 1 item
[0]
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
basis
The paper names GSE90074, GSE27034, GSE159677, GSE59421 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
dsl_operations array · 1 item
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spearman_rho
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source:pmid:41583468
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data:geo:GSE159677
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readers array · 0 items
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data_gaps array · 1 item
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data:geo:GSE159677
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review object · 5 fields
state
partial
machine_critique object · 5 fields
kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
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minimax
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minimax
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2026-11-01T20:11:10Z
independence
single_reader
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verbatim
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verbatim
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5
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128
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paper
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pmid:41583468
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source:pmid:41583468
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manuscript
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PMID 41583468 full text
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data:geo:GSE159677
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activity-reading-sci-2026-11-01
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pmid:41583468
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pmid:41583468
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source:pmid:41583468
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GEO GSE159677
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agent:corpus-assay-engine
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used array · 1 item
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lineage object · 4 fields
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[3]
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[5]
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[7]
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evidence array · 3 items
[0]
ication and its regulatory genes in AS using microarray databases. Specifically, microarray datasets
[1]
AS using microarray databases. Specifically, microarray datasets of AS (GSE90074, GSE27034, GSE59421
[2]
erformed differential expression analysis on microarray data from GSE90074 (AS = 93 and control = 50
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myeloid leukemia mononuclear cells (THP-1). Single-cell RNA sequencing (scRNA-seq) analysis was performed to charac
[1]
r cells (THP-1). Single-cell RNA sequencing (scRNA-seq) analysis was performed to characterize the
[2]
using the R package “geomROC” (version 1.0). scRNA-seq data were analyzed using the R packages “Seu
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kemia mononuclear cells (THP-1). Single-cell RNA sequencing (scRNA-seq) analysis was performed to charac
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Correlations between DEGs and DE-MRs were calculated using Spearman correlation analysis with |Cor| > 0.3 and p < 0.05 to screen for m5C regulator-related genes (MRRGs).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41583468", "kind": "science-record", "revision": 3, "content_hash": "sha256:2b3bb1df6cf38a9e60a8341a6a74b43f7b8c807e9ada2a0e81ac0e6493236c8f", "created_at": "2026-11-01T20:31:33Z", "updated_at": "2026-11-01T22:15:22Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "The role of 5-methylcytosine regulator-related genes in diagnostic and immune regulatory functions in atherosclerosis.", "doi": "10.3389/fimmu.2025.1636323", "pmid": "41583468", "authors": ["Hui Zhao", "Ying Kong", "Pengfei Ding", "Luqun Yang", "Ning Li"], "journal": "Frontiers in immunology", "year": 2025, "abstract": "Background: Atherosclerosis (AS) is a chronic inflammatory disease with a poor prognosis, and 5-methylcytosine (m5C) RNA modification plays a significant role in AS-induced cardio-cerebrovascular diseases (CCVDs). However, the effects of m5C modification and related genes in AS remain unclear.\nMethods: We analyzed the correlations between m5C RNA modification and its regulatory genes in AS using microarray databases. Specifically, microarray datasets of AS (GSE90074, GSE27034, GSE59421, and GSE159677) were obtained from the Gene Expression Omnibus (GEO) database. Following differential expression and Spearman correlation analyses using GSE90074, m5C regulator-related genes (MRRGs) were screened to construct a protein-protein interaction (PPI) network. A least absolute shrinkage and selection operator (LASSO) logistic regression model was constructed and validated using receiver operating characteristic (ROC) curves in GSE90074 and GSE27034 to identify feature genes. Consensus clustering analysis was then performed to classify AS samples into distinct clusters. In addition, Spearman correlation analysis was used to explore the associations between differentially expressed m5C regulators (DE-MRs) and immune cells based on the identified clusters. Weighted gene co-expression network analysis (WGCNA) was applied to identify AS-related module genes. Subsequently, intersecting genes common to module genes and differentially expressed genes (DEGs) across AS-related clusters were considered candidate biomarkers and were validated by quantitative real-time polymerase chain reaction (qRT-PCR) in human myeloid leukemia mononuclear cells (THP-1). Single-cell RNA sequencing (scRNA-seq) analysis was performed to characterize the immune microenvironment of AS. In vitro experiments and genetic interventions were conducted to investigate the effects of the m5C regulator NSUN3 on macrophage function. Finally, a competitive endogenous RNA (ceRNA) network targeting the identified biomarkers was predicted using the miRNet database.\nResults: Based on two differentially expressed m5C regulators (NSUN3 and NSUN5), 546 of 2247 DEGs between AS and control samples were identified as MRRGs for PPI network construction. Twenty hub MRRGs were further incorporated into the LASSO logistic regression model, yielding nine feature genes. Based on these feature genes, AS samples were classified into two clusters, with five immune cell types showing significant differences between clusters. Both NSUN3 and NSUN5 showed the strongest correlations with M0 macrophages. A total of 643 module genes were identified and overlapped with DEGs from the two AS-related clusters, resulting in five biomarkers-MCL1, F13A1, RGS2, Toll-like receptor 8 (TLR8), and TAGAP. The expression patterns of these five biomarkers in the foam cell model were consistent with those observed in public datasets. Furthermore, NSUN3 regulated the production of proinflammatory cytokines in macrophages. Finally, a ceRNA regulatory network was constructed.\nConclusion: Five potential diagnostic biomarkers for AS-MCL1, F13A1, RGS2, TLR8, and TAGAP-were identified. In addition, the m5C regulator NSUN3 plays a critical role in macrophage function, providing experimental evidence that may support the diagnosis and treatment of AS.", "claims": [{"id": "claim-method", "statement": "Correlations between DEGs and DE-MRs were calculated using Spearman correlation analysis with |Cor| > 0.3 and p < 0.05 to screen for m5C regulator-related genes (MRRGs).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41583468", "locator": "sections[4] \"Analysis of differentially expressed m5C regulators and related genes\" paragraph 3", "quote": "Correlations between DEGs and DE-MRs were calculated using Spearman correlation analysis with |Cor| > 0.3 and p < 0.05 to screen for m5C regulator-related genes (MRRGs)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41583468", "locator": "sections[31] \"Data availability statement\" paragraph 2", "quote": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Five potential diagnostic biomarkers for AS—MCL1, F13A1, RGS2, TLR8, and TAGAP—were identified.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:41583468", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "Five potential diagnostic biomarkers for AS—MCL1, F13A1, RGS2, TLR8, and TAGAP—were identified."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Five potential diagnostic biomarkers for AS—MCL1, F13A1, RGS2, TLR8, and TAGAP—were identified.", "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:41583468"], "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:GSE159677"], "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:GSE159677"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:41583468", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fimmu.2025.1636323", "sha256": "sha256:42d81122b27886bb3e788bce86e0e4d2c6cadf78369d4bffac89f20d88fbc211", "bytes": 61616, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fimmu.2025.1636323", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC12827604", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE159677", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE159677", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE159677", "version": null, "note": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM4837523", "GSM4837524", "GSM4837525", "GSM4837526", "GSM4837527", "GSM4837528"], "sample_count": 6, "group_sizes": null, "group_sizes_basis": null, "platform": "18573", "taxon": "Homo sapiens", "title": "Decoding the transcriptome of calcified atherosclerotic plaque at single-cell resolution", "resolution_checked_at": "2026-11-01T18:06:43Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE27034", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE27034", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE27034", "version": null, "note": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM902322", "GSM902323", "GSM902324", "GSM902325", "GSM902326", "GSM902327", "GSM902328", "GSM902329", "GSM902330", "GSM902331", "GSM902332", "GSM902333", "GSM902334", "GSM902335", "GSM902336", "GSM902337", "GSM902338", "GSM902339", "GSM902340", "GSM902341", "GSM902342", "GSM902343", "GSM902344", "GSM902345", "GSM902346", "GSM902347", "GSM902348", "GSM902349", "GSM902350", "GSM902351", "GSM902352", "GSM902353", "GSM902354", "GSM902355", "GSM902356", "GSM902357", "GSM902358"], "sample_count": 37, "group_sizes": null, "group_sizes_basis": null, "platform": "570", "taxon": "Homo sapiens", "title": "Gene expression profiling of peripheral blood mononuclear cells in the setting of peripheral arterial disease", "resolution_checked_at": "2026-11-01T20:16:08Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}, {"id": "data:geo:GSE59421", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE59421", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE59421", "version": null, "note": "The datasets presented in this study can be found in online repositories. 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Specifically, microarray datasets", "AS using microarray databases. Specifically, microarray datasets of AS (GSE90074, GSE27034, GSE59421", "erformed differential expression analysis on microarray data from GSE90074 (AS = 93 and control = 50"], "order_basis": "paper_text_order:473", "id": "assay:1"}, {"role": "data_generation", "definition_id": "scrna_seq", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "unsupported", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["myeloid leukemia mononuclear cells (THP-1). Single-cell RNA sequencing (scRNA-seq) analysis was performed to charac", "r cells (THP-1). 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