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pmid:38802844

Exploring the molecular mechanisms of ferroptosis-related genes in periodontitis: a multi-dataset analysis.

Jili Chen · Lijia Ou · Weizhen Liu · Feng Gao

BMC oral health · 2024 doi:10.1186/s12903-024-04342-2

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

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title
Exploring the molecular mechanisms of ferroptosis-related genes in periodontitis: a multi-dataset analysis.
doi
10.1186/s12903-024-04342-2
pmid
38802844
authors array · 4 items
[0]
Jili Chen
[1]
Lijia Ou
[2]
Weizhen Liu
[3]
Feng Gao
journal
BMC oral health
year
2024
abstract
PURPOSE: This study aims to elucidate the biological functions of ferroptosis-related genes in periodontitis, along with their correlation to tumor microenvironment (TME) features such as immune infiltration. It aims to provide potential diagnostic markers of ferroptosis for clinical management of periodontitis. METHODS: Utilizing the periodontitis-related microarray dataset GSE16134 from the Gene Expression Omnibus (GEO) and a set of 528 ferroptosis-related genes identified in prior studies, this research unveils differentially expressed ferroptosis-related genes in periodontitis. Subsequently, a protein-protein interaction network was constructed. Subtyping of periodontitis was explored, followed by validation through immune cell infiltration and gene set enrichment analyses. Two algorithms, randomForest and SVM(Support Vector Machine), were employed to reveal potential ferroptosis diagnostic markers for periodontitis. The diagnostic efficacy, immune correlation, and potential transcriptional regulatory networks of these markers were further assessed. Finally, potential targeted drugs for differentially expressed ferroptosis markers in periodontitis were predicted. RESULTS: A total of 36 ferroptosis-related genes (30 upregulated, 6 downregulated) were identified from 829 differentially expressed genes between 9 periodontitis samples and the control group. Subsequent machine learning algorithm screening highlighted 4 key genes: SLC1A5(Solute Carrier Family 1 Member 5), SLC2A14(Solute Carrier Family 1 Member 14), LURAP1L(Leucine Rich Adaptor Protein 1 Like), and HERPUD1(Homocysteine Inducible ER Protein With Ubiquitin Like Domain 1). Exploration of these 4 key genes, supported by time-correlated ROC analysis, demonstrated reliability, while immune infiltration results indicated a strong correlation between key genes and immune factors. Furthermore, Gene Set Enrichment Analysis (GSEA) was conducted for the four key genes, revealing enrichment in GO/KEGG pathways that have a significant impact on periodontitis. Finally, the study predicted potential transcriptional regulatory networks and targeted drugs associated with these key genes in periodontitis. CONCLUSIONS: The ferroptosis-related genes identified in this study, including SLC1A5, SLC2A14, LURAP1L, and HERPUD1, may serve as novel diagnostic and therapeutic targets for periodontitis. They are likely involved in the occurrence and development of periodontitis through mechanisms such as immune infiltration, cellular metabolism, and inflammatory chemotaxis, potentially linking the ferroptosis pathway to the progression of periodontitis. Targeted drugs such as flurofamide, L-733060, memantine, tetrabenazine, and WAY-213613 hold promise for potential therapeutic interventions in periodontitis associated with these ferroptosis-related genes.
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All statistical tests were two-sided, with p < 0.05 considered statistically significant. We used Pearson correlation coefficients to assess the relationships between different variables. Specifically, we calculated the correlation coefficients and their associated p-values. For comparisons between two groups, we employed the Wilcoxon test to examine whether there were significant differences in sample means between different groups.
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All statistical tests were two-sided, with p < 0.05 considered statistically significant. We used Pearson correlation coefficients to assess the relationships between different variables. Specifically, we calculated the correlation coefficients and their associated p-values. For comparisons between two groups, we employed the Wilcoxon test to examine whether there were significant differences in sample means between different groups.
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The authors acquired periodontitis-related data for single-cell analysis by downloading the GSE171213 dataset from the NCBI GEO public database. The dataset comprises a total of nine samples, including five from diseased subjects and four from control subjects. The Series Matrix File data for GSE16134 was downloaded from the NCBI GEO public database, with the annotation file labeled as GPL570. The authors confirm that the data supporting the findings of this study are available within the article and its supplementary materials.
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The authors acquired periodontitis-related data for single-cell analysis by downloading the GSE171213 dataset from the NCBI GEO public database. The dataset comprises a total of nine samples, including five from diseased subjects and four from control subjects. The Series Matrix File data for GSE16134 was downloaded from the NCBI GEO public database, with the annotation file labeled as GPL570. The authors confirm that the data supporting the findings of this study are available within the article and its supplementary materials.
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Machine-learning screening identified four key ferroptosis-related genes in periodontitis: SLC1A5, SLC2A14, LURAP1L, and HERPUD1.
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Subsequent machine learning algorithm screening highlighted 4 key genes: SLC1A5(Solute Carrier Family 1 Member 5), SLC2A14(Solute Carrier Family 1 Member 14), LURAP1L(Leucine Rich Adaptor Protein 1 Like), and HERPUD1(Homocysteine Inducible ER Protein With Ubiquitin Like Domain 1).
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Machine-learning screening identified four key ferroptosis-related genes in periodontitis: SLC1A5, SLC2A14, LURAP1L, and HERPUD1.
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The authors acquired periodontitis-related data for single-cell analysis by downloading the GSE171213 dataset from the NCBI GEO public database. The dataset comprises a total of nine samples, including five from diseased subjects and four from control subjects. The Series Matrix File data for GSE16134 was downloaded from the NCBI GEO public database, with the annotation file labeled as GPL570. The authors confirm that the data supporting the findings of this study are available within the article and its supplementary materials.
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METHODS: Utilizing the periodontitis-related microarray dataset GSE16134 from the Gene Expression Om
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All statistical tests were two-sided, with p < 0.05 considered statistically significant. We used Pearson correlation coefficients to assess the relationships between different variables. Specifically, we calculated the correlation coefficients and their associated p-values. For comparisons between two groups, we employed the Wilcoxon test to examine whether there were significant differences in sample means between different groups.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38802844", "kind": "science-record", "revision": 4, "content_hash": "sha256:ed5ead19fc7d5bbd2a5b9ac6cb8560aeabd612855bbf4753edbd97c206a6a493", "created_at": "2026-11-01T19:20:45Z", "updated_at": "2026-11-01T22:54:23Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Exploring the molecular mechanisms of ferroptosis-related genes in periodontitis: a multi-dataset analysis.", "doi": "10.1186/s12903-024-04342-2", "pmid": "38802844", "authors": ["Jili Chen", "Lijia Ou", "Weizhen Liu", "Feng Gao"], "journal": "BMC oral health", "year": 2024, "abstract": "PURPOSE: This study aims to elucidate the biological functions of ferroptosis-related genes in periodontitis, along with their correlation to tumor microenvironment (TME) features such as immune infiltration. It aims to provide potential diagnostic markers of ferroptosis for clinical management of periodontitis.\nMETHODS: Utilizing the periodontitis-related microarray dataset GSE16134 from the Gene Expression Omnibus (GEO) and a set of 528 ferroptosis-related genes identified in prior studies, this research unveils differentially expressed ferroptosis-related genes in periodontitis. Subsequently, a protein-protein interaction network was constructed. Subtyping of periodontitis was explored, followed by validation through immune cell infiltration and gene set enrichment analyses. Two algorithms, randomForest and SVM(Support Vector Machine), were employed to reveal potential ferroptosis diagnostic markers for periodontitis. The diagnostic efficacy, immune correlation, and potential transcriptional regulatory networks of these markers were further assessed. Finally, potential targeted drugs for differentially expressed ferroptosis markers in periodontitis were predicted.\nRESULTS: A total of 36 ferroptosis-related genes (30 upregulated, 6 downregulated) were identified from 829 differentially expressed genes between 9 periodontitis samples and the control group. Subsequent machine learning algorithm screening highlighted 4 key genes: SLC1A5(Solute Carrier Family 1 Member 5), SLC2A14(Solute Carrier Family 1 Member 14), LURAP1L(Leucine Rich Adaptor Protein 1 Like), and HERPUD1(Homocysteine Inducible ER Protein With Ubiquitin Like Domain 1). Exploration of these 4 key genes, supported by time-correlated ROC analysis, demonstrated reliability, while immune infiltration results indicated a strong correlation between key genes and immune factors. Furthermore, Gene Set Enrichment Analysis (GSEA) was conducted for the four key genes, revealing enrichment in GO/KEGG pathways that have a significant impact on periodontitis. Finally, the study predicted potential transcriptional regulatory networks and targeted drugs associated with these key genes in periodontitis.\nCONCLUSIONS: The ferroptosis-related genes identified in this study, including SLC1A5, SLC2A14, LURAP1L, and HERPUD1, may serve as novel diagnostic and therapeutic targets for periodontitis. They are likely involved in the occurrence and development of periodontitis through mechanisms such as immune infiltration, cellular metabolism, and inflammatory chemotaxis, potentially linking the ferroptosis pathway to the progression of periodontitis. Targeted drugs such as flurofamide, L-733060, memantine, tetrabenazine, and WAY-213613 hold promise for potential therapeutic interventions in periodontitis associated with these ferroptosis-related genes.", "claims": [{"id": "claim-method", "statement": "All statistical tests were two-sided, with p < 0.05 considered statistically significant. 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The authors confirm that the data supporting the findings of this study are available within the article and its supplementary materials.", "access_statement_kind": "data_availability_statement", "sample_accessions": ["GSM5220920", "GSM5220921", "GSM5220922", "GSM5220923", "GSM5220924", "GSM5220925", "GSM5220926", "GSM5220927", "GSM5220928", "GSM5220929", "GSM5220930", "GSM5220931"], "sample_count": 12, "group_sizes": null, "group_sizes_basis": null, "platform": "24676", "taxon": "Homo sapiens", "title": "Single-cell RNA sequencing to identify 51248 single cells from periodontal tissues of healthy humans and periodontitis patients with or without treatment", "resolution_checked_at": "2026-11-01T18:46:34Z", "resolution_check": "identifier_resolution_only_no_download_no_licence_read", "downloaded": false, "licence_read": false}}], "gaps": ["asset:data:geo:GSE16134 not downloaded", "asset:data:geo:GSE16134 licence not read", "asset:data:geo:GSE171213 not downloaded", "asset:data:geo:GSE171213 licence not read"]}, "analysis": {"state": "partial", "methods": [{"id": "method-1", "family": "group_comparison", "specific": "wilcoxon", "label": "Group comparison", "dsl_operations": [], "missing_operations": ["group_comparison_wilcoxon"], "expressible": false, "parameters": {}, "data_shapes": ["two_or_more_groups_continuous"], "evidence": {"score": 1.0, "band": "verbatim", "quote": "All statistical tests were two-sided, with p < 0.05 considered statistically significant. 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