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pmid:36816016

Application of an angiogenesis-related genes risk model in lung adenocarcinoma prognosis and immunotherapy.

Jinsong Wang · Xue Cui · Yiming Weng · Jiayan Wei · Xinyi Chen · Peiwei Wang · Tong Wang · Jian Qin · Min Peng

Frontiers in genetics · 2023 doi:10.3389/fgene.2023.1092968

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Data

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title
Application of an angiogenesis-related genes risk model in lung adenocarcinoma prognosis and immunotherapy.
doi
10.3389/fgene.2023.1092968
pmid
36816016
authors array · 9 items
[0]
Jinsong Wang
[1]
Xue Cui
[2]
Yiming Weng
[3]
Jiayan Wei
[4]
Xinyi Chen
[5]
Peiwei Wang
[6]
Tong Wang
[7]
Jian Qin
[8]
Min Peng
journal
Frontiers in genetics
year
2023
abstract
Lung adenocarcinoma (LUAD) is an essential pathological subtype of non-small cell lung cancer and offers a severe problem for worldwide public health. There is mounting proof that angiogenesis is a crucial player in LUAD progression. Consequently, the purpose of this research was to construct a novel LUAD risk assessment model based on genetic markers related to angiogenesis. We accessed The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases for LUAD mRNA sequencing data and clinical information. Based on machine algorithms and bioinformatics, angiogenic gene-related risk scores (RS) were calculated. Patients in the high-risk category had a worse prognosis (p < 0.001) in the discovery TCGA cohort, and the results were confirmed by these three cohorts (validation TCGA cohort, total TCGA cohort, and GSE68465 cohort). Moreover, risk scores for genes involved in angiogenesis were independent risk factors for lung cancer in all four cohorts. The low-risk group was associated with better immune status and lower tumor mutational load. In addition, the somatic mutation study revealed that the low-risk group had a lower mutation frequency than the high-risk group. According to an analysis of tumor stem cell infiltration, HLA expression, and TIDE scores, the low-risk group had higher TIDE scores and HLA expression levels than the high-risk group, and the amount of tumor stem cell infiltration correlated with the risk score. In addition, high-risk groups may benefit from immune checkpoint inhibitors and targeted therapies. In conclusion, we developed an angiogenesis-related gene risk model to predict the prognosis of LUAD patients, which may aid in the classification of patients with LUAD and select medications for LUAD patients.
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A minimum absolute shrinkage and selection operator (LASSO) Cox regression approach was used to construct multivariate models of ARG using the “glmnet” package of R software (Sauerbrei et al., 2007).
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A minimum absolute shrinkage and selection operator (LASSO) Cox regression approach was used to construct multivariate models of ARG using the “glmnet” package of R software (Sauerbrei et al., 2007).
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Patients in the high-risk category had a worse prognosis (p < 0.001) in the discovery TCGA cohort, and the results were confirmed by these three cohorts (validation TCGA cohort, total TCGA cohort, and GSE68465 cohort).
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sample_count
462
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null
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null
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96
taxon
Homo sapiens
title
caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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A minimum absolute shrinkage and selection operator (LASSO) Cox regression approach was used to construct multivariate models of ARG using the “glmnet” package of R software (Sauerbrei et al., 2007).
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survival_analysis
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claim-target-result
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p-value
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note
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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capability object · 3 fields
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Automated Assays Laravel application and simulated adapters
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nothing:replicable_now
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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.
capability object · 4 fields
tier
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capability:computational_analysis
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
true
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[0]
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[1]
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[0]
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.
basis
The paper names GSE68465, GSE50081 in Gene Expression Omnibus Database (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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partial
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T18:28:01Z
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single_reader
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verbatim
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verbatim
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paper
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source:pmid:36816016
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PMID 36816016 full text
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GEO GSE50081
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PMID 36816016 full text
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GEO GSE50081
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agent:corpus-assay-engine
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activity-resolve-GSE50081
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A minimum absolute shrinkage and selection operator (LASSO) Cox regression approach was used to construct multivariate models of ARG using the “glmnet” package of R software (Sauerbrei et al., 2007).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:36816016", "kind": "science-record", "revision": 3, "content_hash": "sha256:69f5fe4b4aa62ea640f5a2bb07bf11d3246762cb5a4807b085a30fdbebe48b61", "created_at": "2026-11-01T19:01:24Z", "updated_at": "2026-11-01T22:08:50Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Application of an angiogenesis-related genes risk model in lung adenocarcinoma prognosis and immunotherapy.", "doi": "10.3389/fgene.2023.1092968", "pmid": "36816016", "authors": ["Jinsong Wang", "Xue Cui", "Yiming Weng", "Jiayan Wei", "Xinyi Chen", "Peiwei Wang", "Tong Wang", "Jian Qin", "Min Peng"], "journal": "Frontiers in genetics", "year": 2023, "abstract": "Lung adenocarcinoma (LUAD) is an essential pathological subtype of non-small cell lung cancer and offers a severe problem for worldwide public health. There is mounting proof that angiogenesis is a crucial player in LUAD progression. Consequently, the purpose of this research was to construct a novel LUAD risk assessment model based on genetic markers related to angiogenesis. We accessed The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases for LUAD mRNA sequencing data and clinical information. Based on machine algorithms and bioinformatics, angiogenic gene-related risk scores (RS) were calculated. Patients in the high-risk category had a worse prognosis (p < 0.001) in the discovery TCGA cohort, and the results were confirmed by these three cohorts (validation TCGA cohort, total TCGA cohort, and GSE68465 cohort). Moreover, risk scores for genes involved in angiogenesis were independent risk factors for lung cancer in all four cohorts. The low-risk group was associated with better immune status and lower tumor mutational load. In addition, the somatic mutation study revealed that the low-risk group had a lower mutation frequency than the high-risk group. According to an analysis of tumor stem cell infiltration, HLA expression, and TIDE scores, the low-risk group had higher TIDE scores and HLA expression levels than the high-risk group, and the amount of tumor stem cell infiltration correlated with the risk score. In addition, high-risk groups may benefit from immune checkpoint inhibitors and targeted therapies. In conclusion, we developed an angiogenesis-related gene risk model to predict the prognosis of LUAD patients, which may aid in the classification of patients with LUAD and select medications for LUAD patients.", "claims": [{"id": "claim-method", "statement": "A minimum absolute shrinkage and selection operator (LASSO) Cox regression approach was used to construct multivariate models of ARG using the “glmnet” package of R software (Sauerbrei et al., 2007).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36816016", "locator": "sections[7] \"2.5 Construction and validation of a prognostic signature based on angiogenesis-related genes\" paragraph 2", "quote": "A minimum absolute shrinkage and selection operator (LASSO) Cox regression approach was used to construct multivariate models of ARG using the “glmnet” package of R software (Sauerbrei et al., 2007)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:36816016", "locator": "sections[29] \"Data availability statement\" paragraph 2", "quote": "The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Patients in the high-risk category had a worse prognosis (p < 0.001) in the discovery TCGA cohort, and the results were confirmed by these three cohorts (validation TCGA cohort, total TCGA cohort, and GSE68465 cohort).", "kind": "quantitative", "target": {"value": 0.001, "unit": "p-value", "tolerance": null, "source": "Patients in the high-risk category had a worse prognosis (p < 0.001) in the discovery TCGA cohort, and the results were confirmed by these three cohorts (validation TCGA cohort, total TCGA cohort, and GSE68465 cohort)."}, "evidence": [{"asset": "source:pmid:36816016", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Patients in the high-risk category had a worse prognosis (p < 0.001) in the discovery TCGA cohort, and the results were confirmed by these three cohorts (validation TCGA cohort, total TCGA cohort, and GSE68465 cohort)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Patients in the high-risk category had a worse prognosis (p < 0.001) in the discovery TCGA cohort, and the results were confirmed by these three cohorts (validation TCGA cohort, total TCGA cohort, and GSE68465 cohort).", "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:36816016"], "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. 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