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pmid:37964257

A novel hypoxia-associated gene signature for prognosis prediction in head and neck squamous cell carcinoma.

Jingyi Luo · Yuejiao Huang · Jiahe Wu · Lin Dai · Mingyou Dong · Bo Cheng

BMC oral health · 2023 doi:10.1186/s12903-023-03489-8

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Experiment

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pmid:37964257
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title
A novel hypoxia-associated gene signature for prognosis prediction in head and neck squamous cell carcinoma.
doi
10.1186/s12903-023-03489-8
pmid
37964257
authors array · 6 items
[0]
Jingyi Luo
[1]
Yuejiao Huang
[2]
Jiahe Wu
[3]
Lin Dai
[4]
Mingyou Dong
[5]
Bo Cheng
journal
BMC oral health
year
2023
abstract
BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is the most common malignant tumor of head and neck, which seriously threatens human life and health. However, the mechanism of hypoxia-associated genes (HAGs) in HNSCC remains unelucidated. This study aims to establish a hypoxia-associated gene signature and the nomogram for predicting the prognosis of patients with HNSCC. METHODS: Previous literature reports provided a list of HAGs. The TCGA database provided genetic and clinical information on HNSCC patients. First, a hypoxia-associated gene risk model was constructed for predicting overall survival (OS) in HNSCC patients and externally validated in four GEO datasets (GSE27020, GSE41613, GSE42743, and GSE117973). Then, immune status and metabolic pathways were analyzed. A nomogram was constructed and assessed the predictive value. Finally, experimental validation of the core genes was performed by qRT-PCR. RESULTS: A HNSCC prognostic model was constructed based on 8 HAGs. This risk model was validated in four external datasets and exhibited high predictive value in various clinical subgroups. Significant differences in immune cell infiltration levels and metabolic pathways were found between high and low risk subgroups. The nomogram was highly accurate for predicting OS in HNSCC patients. CONCLUSIONS: The 8 hypoxia-associated gene signature can serve as novel independent prognostic indicators in HNSCC patients. The nomogram combining the risk score and clinical stage enhanced predictive performance in predicting OS compared to the risk model and clinical characteristics alone.
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To establish a prognostic model, the R package "glmnet" was used to perform the univariate Cox regression and LASSO analyses on the differentially expressed genes screened previously.
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To establish a prognostic model, the R package "glmnet" was used to perform the univariate Cox regression and LASSO analyses on the differentially expressed genes screened previously.
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The datasets presented in this study can be found in GEO (https://www.ncbi.nlm.nih.gov/) and TCGA (https://www.genome.gov/Funded-Programs-Projects/Cancer-Genome-Atlas) databases.
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The risk model predicted 1-year, 3-year, and 5-year survival with AUC values of 0.660, 0.714, and 0.672, respectively.
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sections[14] "Development of prognostic biomarkers for hypoxia-associated genes" paragraph 2
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The risk model predicted 1-year, 3-year, and 5-year survival with AUC values of 0.660, 0.714, and 0.672, respectively (Fig. 2F).
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The risk model predicted 1-year, 3-year, and 5-year survival with AUC values of 0.660, 0.714, and 0.672, respectively.
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sample_count
103
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null
platform
570
taxon
Homo sapiens
title
Oral Cavity Cancer Compared to Adjacent "Normal" Tissue [Validation Set]
resolution_checked_at
2026-11-01T15:39:54Z
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identifier_resolution_only_no_download_no_licence_read
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[3]
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[4]
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[5]
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[6]
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[7]
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To establish a prognostic model, the R package "glmnet" was used to perform the univariate Cox regression and LASSO analyses on the differentially expressed genes screened previously.
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contingency_analysis
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capability object · 3 fields
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candidate
Automated Assays Laravel application and simulated adapters
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cox_ph
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basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
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availability_state
owned
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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.
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tier
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GSE27020
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GSE27020
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[0]
The datasets presented in this study can be found in GEO (https://www.ncbi.nlm.nih.gov/) and TCGA (https://www.genome.gov/Funded-Programs-Projects/Cancer-Genome-Atlas) databases.
basis
The paper names GSE27020, GSE41613, GSE42743, GSE117973 in Gene Expression Omnibus (GEO) database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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minimax
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single_reader
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paper
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data:geo:GSE117973
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GEO GSE117973
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Table S3. The primer sequence information of qPCR experiment. Additional file 2. Details of pa
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To establish a prognostic model, the R package "glmnet" was used to perform the univariate Cox regression and LASSO analyses on the differentially expressed genes screened previously.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37964257", "kind": "science-record", "revision": 4, "content_hash": "sha256:58a1ec450463c55f4115a816a45716594ace0aa8e0cf5e7e8f72750ac50d8747", "created_at": "2026-11-01T19:02:52Z", "updated_at": "2026-11-01T22:10:39Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "A novel hypoxia-associated gene signature for prognosis prediction in head and neck squamous cell carcinoma.", "doi": "10.1186/s12903-023-03489-8", "pmid": "37964257", "authors": ["Jingyi Luo", "Yuejiao Huang", "Jiahe Wu", "Lin Dai", "Mingyou Dong", "Bo Cheng"], "journal": "BMC oral health", "year": 2023, "abstract": "BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is the most common malignant tumor of head and neck, which seriously threatens human life and health. However, the mechanism of hypoxia-associated genes (HAGs) in HNSCC remains unelucidated. This study aims to establish a hypoxia-associated gene signature and the nomogram for predicting the prognosis of patients with HNSCC.\nMETHODS: Previous literature reports provided a list of HAGs. The TCGA database provided genetic and clinical information on HNSCC patients. First, a hypoxia-associated gene risk model was constructed for predicting overall survival (OS) in HNSCC patients and externally validated in four GEO datasets (GSE27020, GSE41613, GSE42743, and GSE117973). Then, immune status and metabolic pathways were analyzed. A nomogram was constructed and assessed the predictive value. Finally, experimental validation of the core genes was performed by qRT-PCR.\nRESULTS: A HNSCC prognostic model was constructed based on 8 HAGs. This risk model was validated in four external datasets and exhibited high predictive value in various clinical subgroups. Significant differences in immune cell infiltration levels and metabolic pathways were found between high and low risk subgroups. The nomogram was highly accurate for predicting OS in HNSCC patients.\nCONCLUSIONS: The 8 hypoxia-associated gene signature can serve as novel independent prognostic indicators in HNSCC patients. The nomogram combining the risk score and clinical stage enhanced predictive performance in predicting OS compared to the risk model and clinical characteristics alone.", "claims": [{"id": "claim-method", "statement": "To establish a prognostic model, the R package \"glmnet\" was used to perform the univariate Cox regression and LASSO analyses on the differentially expressed genes screened previously.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37964257", "locator": "sections[5] \"Development and validation of prognostic features\" paragraph 2", "quote": "To establish a prognostic model, the R package \"glmnet\" was used to perform the univariate Cox regression and LASSO analyses on the differentially expressed genes screened previously."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets presented in this study can be found in GEO (https://www.ncbi.nlm.nih.gov/) and TCGA (https://www.genome.gov/Funded-Programs-Projects/Cancer-Genome-Atlas) databases.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37964257", "locator": "sections[28] \"Availability of data and materials\" paragraph 2", "quote": "The datasets presented in this study can be found in GEO (https://www.ncbi.nlm.nih.gov/) and TCGA (https://www.genome.gov/Funded-Programs-Projects/Cancer-Genome-Atlas) databases."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The risk model predicted 1-year, 3-year, and 5-year survival with AUC values of 0.660, 0.714, and 0.672, respectively.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37964257", "locator": "sections[14] \"Development of prognostic biomarkers for hypoxia-associated genes\" paragraph 2", "quote": "The risk model predicted 1-year, 3-year, and 5-year survival with AUC values of 0.660, 0.714, and 0.672, respectively (Fig. 2F)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The risk model predicted 1-year, 3-year, and 5-year survival with AUC values of 0.660, 0.714, and 0.672, respectively.", "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:37964257"], "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:GSE117973"], "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:GSE117973"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37964257", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12903-023-03489-8", "sha256": 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