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pmid:37234661

Construction and validation of a prognostic prediction model for gastric cancer using a series of genes related to lactate metabolism.

Si-Yu Wang · Yu-Xin Wang · Ao Shen · Rui Jian · Nan An · Shu-Qiang Yuan

Heliyon · 2023 doi:10.1016/j.heliyon.2023.e16157

Paper

complete

Experiment

partial

Data

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Analysis

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pmid:37234661
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2026-11-01T19:01:57Z
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title
Construction and validation of a prognostic prediction model for gastric cancer using a series of genes related to lactate metabolism.
doi
10.1016/j.heliyon.2023.e16157
pmid
37234661
authors array · 6 items
[0]
Si-Yu Wang
[1]
Yu-Xin Wang
[2]
Ao Shen
[3]
Rui Jian
[4]
Nan An
[5]
Shu-Qiang Yuan
journal
Heliyon
year
2023
abstract
Background: Gastric cancer (GC) is one of the most common clinical malignant tumors worldwide, with high morbidity and mortality. The commonly used tumor-node-metastasis (TNM) staging and some common biomarkers have a certain value in predicting the prognosis of GC patients, but they gradually fail to meet the clinical demands. Therefore, we aim to construct a prognostic prediction model for GC patients. Methods: A total of 350 cases were included in the STAD (Stomach adenocarcinoma) entire cohort of TCGA (The Cancer Genome Atlas), including the STAD training cohort of TCGA (n = 176) and the STAD testing cohort of TCGA (n = 174). GSE15459 (n = 191), and GSE62254 (n = 300) were for external validation. Results: Through differential expression analysis and univariate Cox regression analysis in the STAD training cohort of TCGA, we screened out five genes among 600 genes related to lactate metabolism for the construction of our prognostic prediction model. The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model. Gene function analysis, tumor-infiltrating immune cells analysis, tumor microenvironment analysis and clinical treatment exploration were performed to improve the practicability of the model, and hope to provide a new basis for more in-depth study of the molecular mechanism for GC and for clinicians to formulate more reasonable and individualized treatment plans. Conclusions: We screened out and used five genes related to lactate metabolism to develop a prognostic prediction model for GC patients. The prediction performance of the model is confirmed by a series of bioinformatics and statistical analysis.
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The Cox proportional hazard model was used to evaluate the association between risk scores and OS [23].
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The Cox proportional hazard model was used to evaluate the association between risk scores and OS [23].
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The data could be download at (https://portal.gdc.cancer.gov/, https://xenabrowser.net/, and https://www.ncbi.nlm.nih.gov/geo/; GSE15459 and GSE62254) and the code used during the current study are available from the corresponding author on reasonable request.
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The data could be download at (https://portal.gdc.cancer.gov/, https://xenabrowser.net/, and https://www.ncbi.nlm.nih.gov/geo/; GSE15459 and GSE62254) and the code used during the current study are available from the corresponding author on reasonable request.
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The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model.
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The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model.
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sections[0] "Abstract" paragraph 3
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The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model.
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The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model.
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300
group_sizes
null
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null
platform
570
taxon
Homo sapiens
title
Molecular analysis of gastric cancer identifies discrete subtypes associated with distinct clinical characteristics and survival outcomes: the ACRG (Asian Cancer Research Group) study [gastric tumors]
resolution_checked_at
2026-11-01T15:39:55Z
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The Cox proportional hazard model was used to evaluate the association between risk scores and OS [23].
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target-published-estimate
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The threshold the paper applied to its own result, as the paper states it. A run that reproduces the effect is judged against this threshold.
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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: wilcoxon.
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tier
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availability_state
owned
basis
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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reachable
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The data could be download at (https://portal.gdc.cancer.gov/, https://xenabrowser.net/, and https://www.ncbi.nlm.nih.gov/geo/; GSE15459 and GSE62254) and the code used during the current study are available from the corresponding author on reasonable request.
basis
The paper names GSE15459, GSE62254 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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group_comparison_wilcoxon
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null
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MiniMax-M3.1-Flash
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minimax
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minimax
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pmid:37234661
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paper
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pmid:37234661
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source:pmid:37234661
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manuscript
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PMID 37234661 full text
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data:geo:GSE15459
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GEO GSE15459
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PMID 37234661 full text
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GEO GSE15459
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agent:corpus-assay-engine
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agent:minimax-reader
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37234661", "kind": "science-record", "revision": 3, "content_hash": "sha256:2397db7d0674acba0e309724ff5455039f823fc6db8be1f55860dd9b2e7b7793", "created_at": "2026-11-01T19:01:57Z", "updated_at": "2026-11-01T22:09:34Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Construction and validation of a prognostic prediction model for gastric cancer using a series of genes related to lactate metabolism.", "doi": "10.1016/j.heliyon.2023.e16157", "pmid": "37234661", "authors": ["Si-Yu Wang", "Yu-Xin Wang", "Ao Shen", "Rui Jian", "Nan An", "Shu-Qiang Yuan"], "journal": "Heliyon", "year": 2023, "abstract": "Background: Gastric cancer (GC) is one of the most common clinical malignant tumors worldwide, with high morbidity and mortality. The commonly used tumor-node-metastasis (TNM) staging and some common biomarkers have a certain value in predicting the prognosis of GC patients, but they gradually fail to meet the clinical demands. Therefore, we aim to construct a prognostic prediction model for GC patients.\nMethods: A total of 350 cases were included in the STAD (Stomach adenocarcinoma) entire cohort of TCGA (The Cancer Genome Atlas), including the STAD training cohort of TCGA (n = 176) and the STAD testing cohort of TCGA (n = 174). GSE15459 (n = 191), and GSE62254 (n = 300) were for external validation.\nResults: Through differential expression analysis and univariate Cox regression analysis in the STAD training cohort of TCGA, we screened out five genes among 600 genes related to lactate metabolism for the construction of our prognostic prediction model. The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model. Gene function analysis, tumor-infiltrating immune cells analysis, tumor microenvironment analysis and clinical treatment exploration were performed to improve the practicability of the model, and hope to provide a new basis for more in-depth study of the molecular mechanism for GC and for clinicians to formulate more reasonable and individualized treatment plans.\nConclusions: We screened out and used five genes related to lactate metabolism to develop a prognostic prediction model for GC patients. The prediction performance of the model is confirmed by a series of bioinformatics and statistical analysis.", "claims": [{"id": "claim-method", "statement": "The Cox proportional hazard model was used to evaluate the association between risk scores and OS [23].", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37234661", "locator": "sections[12] \"Statistical analysis\" paragraph 2", "quote": "The Cox proportional hazard model was used to evaluate the association between risk scores and OS [23]."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data could be download at (https://portal.gdc.cancer.gov/, https://xenabrowser.net/, and https://www.ncbi.nlm.nih.gov/geo/; GSE15459 and GSE62254) and the code used during the current study are available from the corresponding author on reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37234661", "locator": "sections[28] \"Data availability\" paragraph 2", "quote": "The data could be download at (https://portal.gdc.cancer.gov/, https://xenabrowser.net/, and https://www.ncbi.nlm.nih.gov/geo/; GSE15459 and GSE62254) and the code used during the current study are available from the corresponding author on reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model.", "kind": "quantitative", "target": {"value": 0.05, "unit": "p-value", "tolerance": null, "source": "The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model."}, "evidence": [{"asset": "source:pmid:37234661", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "The internal and external validations showed the same result, that is, patients with higher risk score were associated with poor prognosis (all p < 0.05), and our model works well without regard of patients' age, gender, tumor grade, clinical stage or TNM stage, which supports the availability, validity and stability of our model.", "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:37234661"], "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:GSE15459"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "blocked", "blocked_on": "method:group_comparison_wilcoxon", "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:GSE15459"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:run_analysis blocked on method:group_comparison_wilcoxon"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37234661", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": 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