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pmid:38532933

Novel biomarkers of inflammation-associated immunity in cervical cancer.

Weihong Zhao · Qi Li · Songquan Wen · Yaqin Li · Ying Bai · Zhiyu Tian

Frontiers in oncology · 2024 doi:10.3389/fonc.2024.1351736

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:38532933
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title
Novel biomarkers of inflammation-associated immunity in cervical cancer.
doi
10.3389/fonc.2024.1351736
pmid
38532933
authors array · 6 items
[0]
Weihong Zhao
[1]
Qi Li
[2]
Songquan Wen
[3]
Yaqin Li
[4]
Ying Bai
[5]
Zhiyu Tian
journal
Frontiers in oncology
year
2024
abstract
Background: Cervical cancer (CC) is a highly malignant gynecological cancer with a direct causal link to inflammation, primarily resulting from persistent high-risk human papillomavirus (HPV) infection. Given the challenges in early detection and mid to late-stage treatment, our research aims to identify inflammation-associated immune biomarkers in CC. Methods: Using a bioinformatics approach combined with experimental validation, we integrated two CC datasets (GSE39001 and GSE63514) in the Gene Expression Omnibus (GEO) to eliminate batch effects. Immune-related inflammation differentially expressed genes (DGEs) were obtained by R language identification. Results: This analysis identified 37 inflammation-related DEGs. Subsequently, we discussed the different levels of immune infiltration between CC cases and controls. Weighted gene co-expression network analysis (WGCNA) identified seven immune infiltration-related modules in CC. We identified 15 immune DEGs associated with inflammation at the intersection of these findings. In addition, we constructed a protein interaction network using the String database and screened five hub genes using "CytoHubba": CXC chemokine ligand 8 (CXCL8), CXC chemokine ligand 10 (CXCL10), CX3C chemokine receptor 1 (CX3CR1), Fc gamma receptors 3B (FCGR3B), and SELL. The expression of these five genes in CC was determined by PCR experiments. In addition, we assessed their diagnostic value and further analyzed the association of immune cells with them. Conclusions: Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives.
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The processed data were screened for DEGs through the “limma” package, with screening criteria set at P.adjust < 0.05 and |log2FC|>1 (Fold Change).
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The processed data were screened for DEGs through the “limma” package, with screening criteria set at P.adjust < 0.05 and |log2FC|>1 (Fold Change).
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Publicly available datasets were analyzed in this study. This data can be found here: (GSE39001 and GSE63514) in the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov/geo/).
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Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives.
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Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives.
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Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives.
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Mitosis is the main pathway altered in cervical cancer and is a source of potential markers for screening and survival, and therapeutic targets.
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asset:data:geo:GSE63514 licence not read
[3]
asset:data:geo:GSE63514 not downloaded
[4]
execution.not_run
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review.human_critique
[6]
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[7]
review.machine_critique
assays array · 1 item
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f2132e96ae6c7a4e
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source_hashes object · 1 field
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f2132e96ae6c7a4e
evidence array · 1 item
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The processed data were screened for DEGs through the “limma” package, with screening criteria set at P.adjust < 0.05 and |log2FC|>1 (Fold Change).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38532933", "kind": "science-record", "revision": 4, "content_hash": "sha256:aad6d9af176cd453a2d362f277d172671b1e65a4621d1b0050c539c4fee18a2a", "created_at": "2026-11-01T19:20:28Z", "updated_at": "2026-11-01T22:53:57Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Novel biomarkers of inflammation-associated immunity in cervical cancer.", "doi": "10.3389/fonc.2024.1351736", "pmid": "38532933", "authors": ["Weihong Zhao", "Qi Li", "Songquan Wen", "Yaqin Li", "Ying Bai", "Zhiyu Tian"], "journal": "Frontiers in oncology", "year": 2024, "abstract": "Background: Cervical cancer (CC) is a highly malignant gynecological cancer with a direct causal link to inflammation, primarily resulting from persistent high-risk human papillomavirus (HPV) infection. Given the challenges in early detection and mid to late-stage treatment, our research aims to identify inflammation-associated immune biomarkers in CC.\nMethods: Using a bioinformatics approach combined with experimental validation, we integrated two CC datasets (GSE39001 and GSE63514) in the Gene Expression Omnibus (GEO) to eliminate batch effects. Immune-related inflammation differentially expressed genes (DGEs) were obtained by R language identification.\nResults: This analysis identified 37 inflammation-related DEGs. Subsequently, we discussed the different levels of immune infiltration between CC cases and controls. Weighted gene co-expression network analysis (WGCNA) identified seven immune infiltration-related modules in CC. We identified 15 immune DEGs associated with inflammation at the intersection of these findings. In addition, we constructed a protein interaction network using the String database and screened five hub genes using \"CytoHubba\": CXC chemokine ligand 8 (CXCL8), CXC chemokine ligand 10 (CXCL10), CX3C chemokine receptor 1 (CX3CR1), Fc gamma receptors 3B (FCGR3B), and SELL. The expression of these five genes in CC was determined by PCR experiments. In addition, we assessed their diagnostic value and further analyzed the association of immune cells with them.\nConclusions: Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives.", "claims": [{"id": "claim-method", "statement": "The processed data were screened for DEGs through the “limma” package, with screening criteria set at P.adjust < 0.05 and |log2FC|>1 (Fold Change).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38532933", "locator": "sections[3] \"Data processing and screening of differentially expressed genes\" paragraph 2", "quote": "The processed data were screened for DEGs through the “limma” package, with screening criteria set at P.adjust < 0.05 and |log2FC|>1 (Fold Change)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Publicly available datasets were analyzed in this study. This data can be found here: (GSE39001 and GSE63514) in the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov/geo/).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:38532933", "locator": "sections[25] \"Data availability statement\" paragraph 2", "quote": "Publicly available datasets were analyzed in this study. This data can be found here: (GSE39001 and GSE63514) in the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov/geo/)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:38532933", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Five inflammation- and immune-related genes were identified, aiming to provide new directions for early diagnosis and mid to late-stage treatment of CC from multiple perspectives.", "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:38532933"], "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:GSE39001"], "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:GSE39001"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:38532933", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.3389/fonc.2024.1351736", "sha256": "sha256:ed2de5520089212dd474446d526526160c4d448a5b57459d43d64ba8f5b7dec1", "bytes": 32214, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.3389/fonc.2024.1351736", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC10964772", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE39001", "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=GSE39001", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE39001", "version": null, "note": "Publicly available datasets were analyzed in this study. This data can be found here: (GSE39001 and GSE63514) in the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov/geo/).", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "Publicly available datasets were analyzed in this study. 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This data can be found here: (GSE39001 and GSE63514) in the Gene Expression Omnibus (GEO)(https://www.ncbi.nlm.nih.gov/geo/).", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "Publicly available datasets were analyzed in this study. 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