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pmid:39640604

Oxidative stress gene signature construction to identify subtypes and prognosis of patients with lung adenocarcinoma.

Lan Li · Rujia Qin · Xuefeng Wang · Ke Cao · Fei Lu · Zhengting Chen · Jingyan Gao · Linbo Qiu · Sisong Shu · Han Lu · Li Chang · Wenhui Li

Heliyon · 2024 doi:10.1016/j.heliyon.2024.e38306

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complete

Experiment

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Data

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title
Oxidative stress gene signature construction to identify subtypes and prognosis of patients with lung adenocarcinoma.
doi
10.1016/j.heliyon.2024.e38306
pmid
39640604
authors array · 12 items
[0]
Lan Li
[1]
Rujia Qin
[2]
Xuefeng Wang
[3]
Ke Cao
[4]
Fei Lu
[5]
Zhengting Chen
[6]
Jingyan Gao
[7]
Linbo Qiu
[8]
Sisong Shu
[9]
Han Lu
[10]
Li Chang
[11]
Wenhui Li
journal
Heliyon
year
2024
abstract
Background: Although oxidative stress and malignancies are intimately connected, it is unknown how lung adenocarcinoma (LUAD) is affected by oxidative stress response-related genes (OSRGs).Our goal in this work was to create a genetic signature based on OSRGs that might both predict prognosis and hint to potential treatment options for LUAD. Methods: Clinicopathological and transcriptome information on LUAD patients was obtained from the Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. A model for predicting risk was created using LASSO regression. The TCGA, GSE72094, and GSE41271 cohorts all demonstrated the risk model's prediction ability. Immune cell infiltration was measured using the CIBERSORT method, and the TIDE platform was implemented to evaluate the therapeutic efficacy of immune checkpoint inhibition (ICI). Chemotherapy sensitivity was predicted using drug activity data by the Genomics of Drug Sensitivity. An investigation into gene expression was conducted using qRT-PCR. CCK-8 and transwell assays were employed to look into how DKK1 affected the migration and proliferation of LUAD cells. Results: A gene signature consisting of ANLN, FAM83A, DKK1, LOXL2, RHOV, IGFBP1, CCR2, GNG7, and C11orf16 was efficiently determined and used to calculate a patient-specific risk score, this functioned as a stand-alone biomarker for prediction. Correlations were found between risk scores and immune cell infiltration frequency, ICI therapy response rate, estimated chemotherapeutic drug susceptibility and autophagy-related genes.Furthermore, DKK1 knockdown reduced the ability of LUAD cells to multiply and migrate. Conclusion: Our thorough transcriptome study of OSRGs generated a biological framework effective in forecasting outcome and responsiveness to therapy in LUAD patients.
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To locate DEGs, the 'limma' package was utilized with the following criteria applied: |log 2 fold-change (FC)| > 0.5, FDR <0.05. DEGs and OSRGs were investigated using one-way Cox regression analysis. Then, multicollinearity was decreased using LASSO Cox regression analysis.
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sections[6] "Developing and verifying the prognostic OSRG signature" paragraph 2
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To locate DEGs, the 'limma' package was utilized with the following criteria applied: |log 2 fold-change (FC)| > 0.5, FDR <0.05. DEGs and OSRGs were investigated using one-way Cox regression analysis. Then, multicollinearity was decreased using LASSO Cox regression analysis.
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The data that support the findings of the present study are openly available in GEO (https://www.ncbi.nlm.nih.gov/geo/) and TCGA (https://portal.gdc.cancer.gov/). Data will be made available on request.
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sections[25] "Data availability" paragraph 2
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The data that support the findings of the present study are openly available in GEO (https://www.ncbi.nlm.nih.gov/geo/) and TCGA (https://portal.gdc.cancer.gov/). Data will be made available on request.
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In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the model.
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In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the model.
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sections[17] "The OSRG signature can predict patient prognosis" paragraph 2
quote
In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the model.
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In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the model.
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442
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null
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null
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15048
taxon
Homo sapiens
title
KRAS mutation-associated gene expression, p53 and STK11 mutations, proliferation and immune surveillance in lung adenocarcinoma
resolution_checked_at
2026-11-01T15:39:55Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
false
licence_read
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[0]
asset:data:geo:GSE41271 not downloaded
[1]
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[2]
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[3]
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state
complete
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[0] object · 10 fields
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[0]
cox_ph
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To locate DEGs, the 'limma' package was utilized with the following criteria applied: |log 2 fold-change (FC)| > 0.5, FDR <0.05. DEGs and OSRGs were investigated using one-way Cox regression analysis. Then, multicollinearity was decreased using LASSO Cox regression analysis.
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id
method-2
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differential_expression
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limma_voom
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missing_operations array · 0 items
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fold_change
riteria applied: |log 2 fold-change (FC)| > 0
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count_matrix_with_condition
evidence object · 3 fields
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0.8
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quote
limma
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id
method-3
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network_analysis
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reference_standard_and_test
evidence object · 3 fields
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0.8
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[0] object · 8 fields
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claim-target-result
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null
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complete
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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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capability object · 3 fields
state
complete
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[0] object · 6 fields
capability_id
capability:computational_analysis
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[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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complete
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nothing:replicable_now
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tier
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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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tier
R1
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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
R1
reachable
true
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[0]
GSE72094
[1]
GSE41271
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[0]
GSE72094
[1]
GSE41271
statements array · 1 item
[0]
The data that support the findings of the present study are openly available in GEO (https://www.ncbi.nlm.nih.gov/geo/) and TCGA (https://portal.gdc.cancer.gov/). Data will be made available on request.
basis
The paper names GSE72094, GSE41271 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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cox_ph
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[0]
source:pmid:39640604
[1]
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run_analysis
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[0]
data:geo:GSE41271
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review object · 5 fields
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partial
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extraction_review
reader object · 5 fields
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MiniMax-M3.1-Flash
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minimax
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minimax
read_at
2026-11-01T19:41:08Z
independence
single_reader
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verbatim
availability
verbatim
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5
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15550
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2418
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[0] object · 4 fields
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extraction
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minimax
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[2]
review.human_critique
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absent
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not_run
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null
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pmid:39640604
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paper
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pmid:39640604
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source:pmid:39640604
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manuscript
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PMID 39640604 full text
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data:geo:GSE41271
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dataset
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GEO GSE41271
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[0] object · 4 fields
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type
classification
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[0] object · 3 fields
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pmid:39640604
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paper
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pmid:39640604
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source:pmid:39640604
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manuscript
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PMID 39640604 full text
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data:geo:GSE41271
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dataset
label
GEO GSE41271
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agent:corpus-assay-engine
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extraction
used array · 1 item
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agent:minimax-reader
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null
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[3]
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[0] object · 11 fields
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apoptosis_assay
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gene expression was conducted using qRT-PCR. CCK-8 and transwell assays were employed to look i
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nd autophagy-related genes.Furthermore, DKK1 knockdown reduced the ability of LUAD cells to multipl
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paper_text_order:1662
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iler' program. Cell culture and quantitative real-time PCR (qRT-PCR) The Institute of Biochemistry and
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assay:3
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[0]
ology (Shanghai, PR China) supplied the B2B, A549, H1734, H1650, and H1299 human lung cancer c
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paper_text_order:2655
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assay:4
[4] object · 11 fields
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analysis
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supported
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f2132e96ae6c7a4e
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To locate DEGs, the 'limma' package was utilized with the following criteria applied: |log 2 fold-change (FC)| > 0.5, FDR <0.05. DEGs and OSRGs were investigated using one-way Cox regression analysis. Then, multicollinearity was decreased using LASSO Cox regression analysis.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:39640604", "kind": "science-record", "revision": 3, "content_hash": "sha256:5f3179934dbf620ce602bc4de94c544d57cf92d52c23e726412a4196f97142f2", "created_at": "2026-11-01T20:29:55Z", "updated_at": "2026-11-01T22:13:16Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Oxidative stress gene signature construction to identify subtypes and prognosis of patients with lung adenocarcinoma.", "doi": "10.1016/j.heliyon.2024.e38306", "pmid": "39640604", "authors": ["Lan Li", "Rujia Qin", "Xuefeng Wang", "Ke Cao", "Fei Lu", "Zhengting Chen", "Jingyan Gao", "Linbo Qiu", "Sisong Shu", "Han Lu", "Li Chang", "Wenhui Li"], "journal": "Heliyon", "year": 2024, "abstract": "Background: Although oxidative stress and malignancies are intimately connected, it is unknown how lung adenocarcinoma (LUAD) is affected by oxidative stress response-related genes (OSRGs).Our goal in this work was to create a genetic signature based on OSRGs that might both predict prognosis and hint to potential treatment options for LUAD.\nMethods: Clinicopathological and transcriptome information on LUAD patients was obtained from the Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. A model for predicting risk was created using LASSO regression. The TCGA, GSE72094, and GSE41271 cohorts all demonstrated the risk model's prediction ability. Immune cell infiltration was measured using the CIBERSORT method, and the TIDE platform was implemented to evaluate the therapeutic efficacy of immune checkpoint inhibition (ICI). Chemotherapy sensitivity was predicted using drug activity data by the Genomics of Drug Sensitivity. An investigation into gene expression was conducted using qRT-PCR. CCK-8 and transwell assays were employed to look into how DKK1 affected the migration and proliferation of LUAD cells.\nResults: A gene signature consisting of ANLN, FAM83A, DKK1, LOXL2, RHOV, IGFBP1, CCR2, GNG7, and C11orf16 was efficiently determined and used to calculate a patient-specific risk score, this functioned as a stand-alone biomarker for prediction. Correlations were found between risk scores and immune cell infiltration frequency, ICI therapy response rate, estimated chemotherapeutic drug susceptibility and autophagy-related genes.Furthermore, DKK1 knockdown reduced the ability of LUAD cells to multiply and migrate.\nConclusion: Our thorough transcriptome study of OSRGs generated a biological framework effective in forecasting outcome and responsiveness to therapy in LUAD patients.", "claims": [{"id": "claim-method", "statement": "To locate DEGs, the 'limma' package was utilized with the following criteria applied: |log 2 fold-change (FC)| > 0.5, FDR <0.05. DEGs and OSRGs were investigated using one-way Cox regression analysis. Then, multicollinearity was decreased using LASSO Cox regression analysis.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39640604", "locator": "sections[6] \"Developing and verifying the prognostic OSRG signature\" paragraph 2", "quote": "To locate DEGs, the 'limma' package was utilized with the following criteria applied: |log 2 fold-change (FC)| > 0.5, FDR <0.05. DEGs and OSRGs were investigated using one-way Cox regression analysis. Then, multicollinearity was decreased using LASSO Cox regression analysis."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data that support the findings of the present study are openly available in GEO (https://www.ncbi.nlm.nih.gov/geo/) and TCGA (https://portal.gdc.cancer.gov/). Data will be made available on request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:39640604", "locator": "sections[25] \"Data availability\" paragraph 2", "quote": "The data that support the findings of the present study are openly available in GEO (https://www.ncbi.nlm.nih.gov/geo/) and TCGA (https://portal.gdc.cancer.gov/). Data will be made available on request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the model.", "kind": "quantitative", "target": {"value": 0.001, "unit": "p-value", "tolerance": null, "source": "In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the model."}, "evidence": [{"asset": "source:pmid:39640604", "locator": "sections[17] \"The OSRG signature can predict patient prognosis\" paragraph 2", "quote": "In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the model."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "In training set TCGA-LUAD data, the prognosis was worse for high-risk cohort (P < 0.001) (Fig. 5A), and expected AUC values of data sets at 1, 3, and 5 years were 0.760, 0.714, and 0.660, correspondingly (Fig. 5B), indicating the outstanding predictive value of the 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:39640604"], "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:GSE41271"], "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:GSE41271"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:39640604", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1016/j.heliyon.2024.e38306", "sha256": "sha256:462a4282b692cf653d463702903bc1039665cacbfee43ec3f728c41da3e4b48a", "bytes": 54005, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1016/j.heliyon.2024.e38306", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC11619975", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE41271", "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=GSE41271", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE41271", "version": null, "note": "The data that support the findings of the present study are openly available in GEO (https://www.ncbi.nlm.nih.gov/geo/) and TCGA (https://portal.gdc.cancer.gov/). Data will be made available on request.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The data that support the findings of the present study are openly available in GEO (https://www.ncbi.nlm.nih.gov/geo/) and TCGA (https://portal.gdc.cancer.gov/). 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