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pmid:39402186

The co-expression of Crohn's disease and colon cancer network was analyzed by bioinformatics-CXCL1 tumour microenvironment and prognosis-related gene CXCL1.

Zijuan Mao · Yuyang Gu · Ganxue Tao · Qiang Dai · Yangjie Xu · Zhenghua Fei

Discover oncology · 2024 doi:10.1007/s12672-024-01423-0

Paper

complete

Experiment

complete

Data

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Execution

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title
The co-expression of Crohn's disease and colon cancer network was analyzed by bioinformatics-CXCL1 tumour microenvironment and prognosis-related gene CXCL1.
doi
10.1007/s12672-024-01423-0
pmid
39402186
authors array · 6 items
[0]
Zijuan Mao
[1]
Yuyang Gu
[2]
Ganxue Tao
[3]
Qiang Dai
[4]
Yangjie Xu
[5]
Zhenghua Fei
journal
Discover oncology
year
2024
abstract
PURPOSE: This study aimed to investigate the molecular links and mechanisms between Crohn's disease (CD) and colorectal cancer (CRC). METHODS: This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'. The Gene Ontology and the Kyoto Encyclopedia of Genes and Genomes explored DEG functions, and the Search Tool for the Retrieval of Interacting Genes (STRING) informed the protein-protein interaction network construction visualized in Cytoscape (version 3.7.2). Cyto-Hubba identified key genes, whose biomarker potential for CD and CRC was evaluated. RESULTS: The study discovered 61 DEGs, with 44 up- and 17 down-regulated, linked to immune responses and signaling pathways. CXCL1, highly expressed in colon cancer, correlated with better prognosis and lower staging. It also showed associations with immune infiltration and checkpoint molecules, suggesting a role in cancer progression and retreat. CONCLUSION: CXCL1 may play a role in the development of colorectal cancer from inflammatory bowel disease.
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This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'.
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This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'.
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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. The data that support the results of the current study is available on The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) websites.
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The study discovered 61 DEGs, with 44 up- and 17 down-regulated, linked to immune responses and signaling pathways.
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sample_count
388
group_sizes
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null
platform
13158
taxon
Homo sapiens
title
Intestinal epithelial microvilli are abnormal in Crohn's disease
resolution_checked_at
2026-11-01T18:46:34Z
resolution_check
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downloaded
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licence_read
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[3]
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[4]
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[5]
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This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'.
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tier
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availability_state
owned
basis
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data object · 6 fields
tier
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accessions array · 3 items
[0]
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statements array · 1 item
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The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. The data that support the results of the current study is available on The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) websites.
basis
The paper names GSE112366, GSE110224, GSE102133 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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state
partial
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kind
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minimax
provider_family
minimax
read_at
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independence
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method
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verbatim
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dataset
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PMID 39402186 full text
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GEO GSE102133
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activity-resolve-GSE102133
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This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'.
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39402186", "kind": "science-record", "revision": 4, "content_hash": "sha256:275a86976ff7a190eda335a96b1e9b4eae364d197aeadee572d4ee056fe9b1c2", "created_at": "2026-11-01T20:29:38Z", "updated_at": "2026-11-01T22:55:24Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "The co-expression of Crohn's disease and colon cancer network was analyzed by bioinformatics-CXCL1 tumour microenvironment and prognosis-related gene CXCL1.", "doi": "10.1007/s12672-024-01423-0", "pmid": "39402186", "authors": ["Zijuan Mao", "Yuyang Gu", "Ganxue Tao", "Qiang Dai", "Yangjie Xu", "Zhenghua Fei"], "journal": "Discover oncology", "year": 2024, "abstract": "PURPOSE: This study aimed to investigate the molecular links and mechanisms between Crohn's disease (CD) and colorectal cancer (CRC).\nMETHODS: This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'. The Gene Ontology and the Kyoto Encyclopedia of Genes and Genomes explored DEG functions, and the Search Tool for the Retrieval of Interacting Genes (STRING) informed the protein-protein interaction network construction visualized in Cytoscape (version 3.7.2). Cyto-Hubba identified key genes, whose biomarker potential for CD and CRC was evaluated.\nRESULTS: The study discovered 61 DEGs, with 44 up- and 17 down-regulated, linked to immune responses and signaling pathways. CXCL1, highly expressed in colon cancer, correlated with better prognosis and lower staging. It also showed associations with immune infiltration and checkpoint molecules, suggesting a role in cancer progression and retreat.\nCONCLUSION: CXCL1 may play a role in the development of colorectal cancer from inflammatory bowel disease.", "claims": [{"id": "claim-method", "statement": "This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39402186", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "This study used the Gene Expression Omnibus (GEO) database to identify Differentially expressed genes (DEGs) in CD (GSE112366) and CRC (GSE110224), analyzed by 'edgeR' and 'limma'."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE102133"], "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:GSE102133"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39402186", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1007/s12672-024-01423-0", "sha256": "sha256:d6bcea2edc4d9dfb8979a1637e976a6ee4fdc74f97437c48510167b8be49f183", "bytes": 33307, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1007/s12672-024-01423-0", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC11479648", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE102133", "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=GSE102133", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE102133", "version": null, "note": "The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. The data that support the results of the current study is available on The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) websites.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. 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