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pmid:36923072

Identification of ferroptosis-related genes in ulcerative colitis: a diagnostic model with machine learning.

Rui Qian · Min Tang · Zichen Ouyang · Honghui Cheng · Sizhong Xing

Annals of translational medicine · 2023 doi:10.21037/atm-23-276

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complete

Experiment

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Data

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Analysis

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title
Identification of ferroptosis-related genes in ulcerative colitis: a diagnostic model with machine learning.
doi
10.21037/atm-23-276
pmid
36923072
authors array · 5 items
[0]
Rui Qian
[1]
Min Tang
[2]
Zichen Ouyang
[3]
Honghui Cheng
[4]
Sizhong Xing
journal
Annals of translational medicine
year
2023
abstract
Background: Ulcerative colitis (UC) is an idiopathic, chronic disorder characterized by inflammation, injury, and disruption of the colonic mucosa. However, there are still many difficulties in the diagnosis and differential diagnosis of UC. An increasing amount of research has shown a connection between ferroptosis and the etiology of UC. Therefore, our study aimed to identify the key genes related to ferroptosis in UC to provide new ideas for diagnosis UC. Methods: Gene expression profiles of normal and UC samples were extracted from the Gene Expression Omnibus (GEO) database. By combining differentially expressed genes (DEGs), Weighted correlation network analysis (WGCNA) genes, and ferroptosis-related genes, hub genes were identified and then screened using Lasso regression. Based on the key genes, gene ontology (GO) and gene set enrichment analysis (GSEA) analyses were performed. We used NaiveBeyas, Logistic, IBk, and RandomForest algorithms to build a disease diagnosis model using the hub genes. The model was validated using GSE87473 as the validation set. Results: Gene expression matrices of GSE87466 and GSE75214 were downloaded from the GEO database, including 184 UC patients and 43 control samples. A total of 699 DEGs were obtained. From FerrDb, 565 genes related to ferroptosis were identified. The 1,513 genes with the highest absolute correlation coefficient value in the MEblue module were obtained from WGCNA analysis. Five hub genes (LCN2, MUC1, PARP8, PLIN2, and TIMP1) were identified using the Lasso regression algorithm based on the overlapped DEGs, WGCNA-identified genes, and ferroptosis-related genes. GO and GSEA analyses revealed that 5 hub genes were identified as being involved in the negative regulation of transcription by competitive promoter binding, cellular response to citrate cycle_tca_cycle, cytosolic_dna_sensing pathway, UV-A, and beta-alanine metabolism. The logistic algorithm's values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods. Conclusions: The previously described hub genes were identified as being intimately related to ferroptosis in UC and capable of distinguishing UC patients from controls. By detecting the expression of several genes, this model may aid in diagnosing UC and understanding the etiology and treatment of the disease.
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Five hub genes (LCN2, MUC1, PARP8, PLIN2, and TIMP1) were identified by further screening using the Lasso regression algorithm (Figure 4B).
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sections[15] "Identification of hub genes associated by intersection and lasso regression" paragraph 2
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Five hub genes (LCN2, MUC1, PARP8, PLIN2, and TIMP1) were identified by further screening using the Lasso regression algorithm (Figure 4B).
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Gene expression matrices of GSE87466 and GSE75214 were downloaded from the GEO database, including 184 UC patients and 43 control samples.
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The logistic algorithm’s values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods.
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The logistic algorithm’s values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods.
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The logistic algorithm’s values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods.
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sample_count
127
group_sizes
null
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null
platform
13158
taxon
Homo sapiens
title
Gene expression profiling of mucosal biopsies from pediatric or adult patients with moderately to severely active ulcerative colitis
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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asset:data:geo:GSE87473 licence not read
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state
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label
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quote
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specific
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missing_operations array · 0 items
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data_shapes array · 0 items
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quote
Five hub genes (LCN2, MUC1, PARP8, PLIN2, and TIMP1) were identified by further screening using the Lasso regression algorithm (Figure 4B).
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method.reader_named_unmapped
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Automated Assays Laravel application and simulated adapters
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: logistic.
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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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Gene expression matrices of GSE87466 and GSE75214 were downloaded from the GEO database, including 184 UC patients and 43 control samples.
basis
The paper names GSE87466, GSE75214, GSE87473 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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data:geo:GSE75214
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state
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T18:33:40Z
independence
single_reader
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paper
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pmid:36923072
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source:pmid:36923072
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manuscript
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PMID 36923072 full text
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data:geo:GSE75214
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GEO GSE75214
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classification
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pmid:36923072
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PMID 36923072 full text
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data:geo:GSE75214
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dataset
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GEO GSE75214
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agent:corpus-assay-engine
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agent:minimax-reader
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activity-resolve-GSE75214
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accession_resolution
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agent:corpus-assay-engine
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36923072", "kind": "science-record", "revision": 2, "content_hash": "sha256:5d7def79ab21a7e872fe4811d56dfbb5b7d21cfcb96f566b6768ca85b734a9a9", "created_at": "2026-11-01T19:01:34Z", "updated_at": "2026-11-01T21:30:22Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of ferroptosis-related genes in ulcerative colitis: a diagnostic model with machine learning.", "doi": "10.21037/atm-23-276", "pmid": "36923072", "authors": ["Rui Qian", "Min Tang", "Zichen Ouyang", "Honghui Cheng", "Sizhong Xing"], "journal": "Annals of translational medicine", "year": 2023, "abstract": "Background: Ulcerative colitis (UC) is an idiopathic, chronic disorder characterized by inflammation, injury, and disruption of the colonic mucosa. However, there are still many difficulties in the diagnosis and differential diagnosis of UC. An increasing amount of research has shown a connection between ferroptosis and the etiology of UC. Therefore, our study aimed to identify the key genes related to ferroptosis in UC to provide new ideas for diagnosis UC.\nMethods: Gene expression profiles of normal and UC samples were extracted from the Gene Expression Omnibus (GEO) database. By combining differentially expressed genes (DEGs), Weighted correlation network analysis (WGCNA) genes, and ferroptosis-related genes, hub genes were identified and then screened using Lasso regression. Based on the key genes, gene ontology (GO) and gene set enrichment analysis (GSEA) analyses were performed. We used NaiveBeyas, Logistic, IBk, and RandomForest algorithms to build a disease diagnosis model using the hub genes. The model was validated using GSE87473 as the validation set.\nResults: Gene expression matrices of GSE87466 and GSE75214 were downloaded from the GEO database, including 184 UC patients and 43 control samples. A total of 699 DEGs were obtained. From FerrDb, 565 genes related to ferroptosis were identified. The 1,513 genes with the highest absolute correlation coefficient value in the MEblue module were obtained from WGCNA analysis. Five hub genes (LCN2, MUC1, PARP8, PLIN2, and TIMP1) were identified using the Lasso regression algorithm based on the overlapped DEGs, WGCNA-identified genes, and ferroptosis-related genes. GO and GSEA analyses revealed that 5 hub genes were identified as being involved in the negative regulation of transcription by competitive promoter binding, cellular response to citrate cycle_tca_cycle, cytosolic_dna_sensing pathway, UV-A, and beta-alanine metabolism. The logistic algorithm's values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods.\nConclusions: The previously described hub genes were identified as being intimately related to ferroptosis in UC and capable of distinguishing UC patients from controls. By detecting the expression of several genes, this model may aid in diagnosing UC and understanding the etiology and treatment of the disease.", "claims": [{"id": "claim-method", "statement": "Five hub genes (LCN2, MUC1, PARP8, PLIN2, and TIMP1) were identified by further screening using the Lasso regression algorithm (Figure 4B).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36923072", "locator": "sections[15] \"Identification of hub genes associated by intersection and lasso regression\" paragraph 2", "quote": "Five hub genes (LCN2, MUC1, PARP8, PLIN2, and TIMP1) were identified by further screening using the Lasso regression algorithm (Figure 4B)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Gene expression matrices of GSE87466 and GSE75214 were downloaded from the GEO database, including 184 UC patients and 43 control samples.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36923072", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Gene expression matrices of GSE87466 and GSE75214 were downloaded from the GEO database, including 184 UC patients and 43 control samples."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The logistic algorithm’s values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:36923072", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The logistic algorithm’s values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The logistic algorithm’s values of the area under the curve (AUC)were 1.000 and 0.995 for training and validation cohorts, and sensitivity is 0.962, specificity is 1.000, respectively, as determined by comparing various methods.", "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:36923072"], "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:GSE75214"], "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:GSE75214"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:36923072", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.21037/atm-23-276", "sha256": 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43 control samples.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "Gene expression matrices of GSE87466 and GSE75214 were downloaded from the GEO database, including 184 UC patients and 43 control samples.", "access_statement_kind": "repository_route_statement", "sample_accessions": ["GSM1426071", "GSM1426072", "GSM1426073", "GSM1426074", "GSM1426075", "GSM1426076", "GSM1426077", "GSM1426078", "GSM1426079", "GSM1426080", "GSM1426081", "GSM1426082", "GSM1426083", "GSM1426084", "GSM1426085", "GSM1426086", "GSM1426087", "GSM1426088", "GSM1426089", "GSM1426090", "GSM1426091", "GSM1426092", "GSM1426093", "GSM1426094", "GSM1426095", "GSM1426096", "GSM1426097", "GSM1426098", "GSM1426099", "GSM1426100", "GSM1426101", "GSM1426102", "GSM1426103", "GSM1426104", "GSM1426105", "GSM1426106", "GSM1426107", "GSM1426108", "GSM1426109", "GSM1426110", "GSM1426111", "GSM1426112", "GSM1426113", "GSM1426114", "GSM1426115", "GSM1426116", "GSM1426117", 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