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pmid:37096455

Identification and validation of the model consisting of DDX49, EGFR, and T-stage as a possible risk factor for lymph node metastasis in patients with lung cancer.

Zhimin Zhang · Xiaojuan Lian · Hongxu Yue · Debing Xiang · Zhongxi Niu

Thoracic cancer · 2023 doi:10.1111/1759-7714.14892

Paper

complete

Experiment

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Data

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Analysis

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title
Identification and validation of the model consisting of DDX49, EGFR, and T-stage as a possible risk factor for lymph node metastasis in patients with lung cancer.
doi
10.1111/1759-7714.14892
pmid
37096455
authors array · 5 items
[0]
Zhimin Zhang
[1]
Xiaojuan Lian
[2]
Hongxu Yue
[3]
Debing Xiang
[4]
Zhongxi Niu
journal
Thoracic cancer
year
2023
abstract
INTRODUCTION: The lymph node metastasis stage of lung cancer is an important decisive factor in the need for postoperative adjuvant treatment and the difference between stage IIIa and stage IIIB that is the necessary information to distinguish whether surgery can be performed or not. The specificity of the clinical diagnosis of lung cancer with lymph node metastasis cannot meet the requirements of preoperative evaluation of surgical indications and prediction of surgical removal range in lung cancer. METHODS: This was an early experimental laboratory trial. The model identification data included the RNA sequence data of 10 patients from our clinical data and 188 patients with lung cancer from The Cancer Genome Atlas dataset. The model development and validation data consisted of RNA sequence data for 537 cases from the Gene Expression Omnibus dataset. We explore the predictive value of the model on two independent clinical data. RESULTS: A higher specificity of diagnostic model for patients with lung cancer with lymph node metastases consisted of DDX49, EGFR, and tumor stage (T-stage), which were the independent predictive factors. The area under the curve value, specificity, and sensitivity for predicting lymph node metastases were 0.835, 70.4%, and 78.9% at RNA expression level in the training group, and 0.681, 73.2%, and 75.7% at RNA expression level in the validation group as shown as in result part. To verify the predictive performance of the combined model for lymph node metastases, we downloaded the GSE30219 data set (n = 291) and the GSE31210 data set (n = 246) from the Gene Expression Omnibus (GEO) database as the training group and validation group, respectively. In addition, the model had a higher specificity for predicting lymph node metastases in independent tissue samples. CONCLUSIONS: Determination of DDX49, EGFR, and T-stage could form a novel prediction model to improve the diagnostic efficacy of lymph node metastasis in clinical application.
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Independent predictors for lymph node metastasis were analyzed by stepwise logistic regression analysis, with age, gender, histology, T‐ and clinical stage, and nine candidate genes as initial covariates.
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Independent predictors for lymph node metastasis were analyzed by stepwise logistic regression analysis, with age, gender, histology, T‐ and clinical stage, and nine candidate genes as initial covariates.
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sections[22] "DATA AVAILABILITY STATEMENT" paragraph 2
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Data and materials will be shared.
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The combined DDX49, EGFR, and T-stage model showed an AUC of 0.835 in the training group and 0.681 in the validation group for predicting lymph node metastases.
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sections[0] "Abstract" paragraph 3
quote
The area under the curve value, specificity, and sensitivity for predicting lymph node metastases were 0.835, 70.4%, and 78.9% at RNA expression level in the training group, and 0.681, 73.2%, and 75.7% at RNA expression level in the validation group as shown as in result part.
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The combined DDX49, EGFR, and T-stage model showed an AUC of 0.835 in the training group and 0.681 in the validation group for predicting lymph node metastases.
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GSM773785
sample_count
246
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Gene expression data for pathological stage I-II lung adenocarcinomas
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
downloaded
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licence_read
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[0]
asset:data:geo:GSE30219 not downloaded
[1]
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[2]
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[3]
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analysis object · 4 fields
state
complete
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[0] object · 10 fields
id
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family
regression_modelling
specific
logistic
label
Regression modelling
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[0]
glm_logit_fit
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predictors_and_outcome
evidence object · 3 fields
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quote
Independent predictors for lymph node metastasis were analyzed by stepwise logistic regression analysis, with age, gender, histology, T‐ and clinical stage, and nine candidate genes as initial covariates.
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id
method-2
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diagnostic_evaluation
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label
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reference_standard_and_test
evidence object · 3 fields
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quote
ROC curve
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capability object · 3 fields
state
complete
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capability_id
capability:computational_analysis
label
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assay_families array · 9 items
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[4]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
complete
tier
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blocked_on
nothing:replicable_now
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method object · 5 fields
tier
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glm_logit_fit
missing_operations array · 0 items
basis
The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: logistic.
capability object · 4 fields
tier
R1
capability_id
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
accessions array · 2 items
[0]
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[1]
GSE31210
resolved_accessions array · 2 items
[0]
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statements array · 1 item
[0]
Data and materials will be shared.
basis
The paper names GSE30219, GSE31210 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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glm_logit_fit
assets array · 2 items
[0]
source:pmid:37096455
[1]
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steps array · 1 item
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must_build object · 5 fields
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data_gaps array · 1 item
[0]
data:geo:GSE30219
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review object · 5 fields
state
partial
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kind
extraction_review
reader object · 5 fields
model
MiniMax-M3.1-Flash
provider
minimax
provider_family
minimax
read_at
2026-11-01T18:37:39Z
independence
single_reader
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method
verbatim
availability
verbatim
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extraction
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type
paper
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id
source:pmid:37096455
type
manuscript
label
PMID 37096455 full text
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id
data:geo:GSE30219
type
dataset
label
GEO GSE30219
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[0] object · 4 fields
id
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type
classification
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paper
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source:pmid:37096455
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PMID 37096455 full text
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data:geo:GSE30219
type
dataset
label
GEO GSE30219
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agent:corpus-assay-engine
[1] object · 4 fields
id
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type
extraction
used array · 1 item
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agent
agent:minimax-reader
[2] object · 4 fields
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activity-resolve-GSE30219
type
accession_resolution
used array · 1 item
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agent
agent:corpus-assay-engine
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[0] object · 3 fields
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lineage object · 4 fields
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[4]
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[6]
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assays array · 1 item
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role
analysis
definition_id
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supported
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Independent predictors for lymph node metastasis were analyzed by stepwise logistic regression analysis, with age, gender, histology, T‐ and clinical stage, and nine candidate genes as initial covariates.
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analysis_only
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37096455", "kind": "science-record", "revision": 4, "content_hash": "sha256:a360e139e826a53ef7dd42a10dbb9a2b956ead7fa40e010e8a7f2de6806dfc55", "created_at": "2026-11-01T19:01:46Z", "updated_at": "2026-11-01T22:51:46Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and validation of the model consisting of DDX49, EGFR, and T-stage as a possible risk factor for lymph node metastasis in patients with lung cancer.", "doi": "10.1111/1759-7714.14892", "pmid": "37096455", "authors": ["Zhimin Zhang", "Xiaojuan Lian", "Hongxu Yue", "Debing Xiang", "Zhongxi Niu"], "journal": "Thoracic cancer", "year": 2023, "abstract": "INTRODUCTION: The lymph node metastasis stage of lung cancer is an important decisive factor in the need for postoperative adjuvant treatment and the difference between stage IIIa and stage IIIB that is the necessary information to distinguish whether surgery can be performed or not. The specificity of the clinical diagnosis of lung cancer with lymph node metastasis cannot meet the requirements of preoperative evaluation of surgical indications and prediction of surgical removal range in lung cancer.\nMETHODS: This was an early experimental laboratory trial. The model identification data included the RNA sequence data of 10 patients from our clinical data and 188 patients with lung cancer from The Cancer Genome Atlas dataset. The model development and validation data consisted of RNA sequence data for 537 cases from the Gene Expression Omnibus dataset. We explore the predictive value of the model on two independent clinical data.\nRESULTS: A higher specificity of diagnostic model for patients with lung cancer with lymph node metastases consisted of DDX49, EGFR, and tumor stage (T-stage), which were the independent predictive factors. The area under the curve value, specificity, and sensitivity for predicting lymph node metastases were 0.835, 70.4%, and 78.9% at RNA expression level in the training group, and 0.681, 73.2%, and 75.7% at RNA expression level in the validation group as shown as in result part. To verify the predictive performance of the combined model for lymph node metastases, we downloaded the GSE30219 data set (n = 291) and the GSE31210 data set (n = 246) from the Gene Expression Omnibus (GEO) database as the training group and validation group, respectively. In addition, the model had a higher specificity for predicting lymph node metastases in independent tissue samples.\nCONCLUSIONS: Determination of DDX49, EGFR, and T-stage could form a novel prediction model to improve the diagnostic efficacy of lymph node metastasis in clinical application.", "claims": [{"id": "claim-method", "statement": "Independent predictors for lymph node metastasis were analyzed by stepwise logistic regression analysis, with age, gender, histology, T‐ and clinical stage, and nine candidate genes as initial covariates.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37096455", "locator": "sections[9] \"Statistical analysis\" paragraph 2", "quote": "Independent predictors for lymph node metastasis were analyzed by stepwise logistic regression analysis, with age, gender, histology, T‐ and clinical stage, and nine candidate genes as initial covariates."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data and materials will be shared.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37096455", "locator": "sections[22] \"DATA AVAILABILITY STATEMENT\" paragraph 2", "quote": "Data and materials will be shared."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The combined DDX49, EGFR, and T-stage model showed an AUC of 0.835 in the training group and 0.681 in the validation group for predicting lymph node metastases.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:37096455", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The area under the curve value, specificity, and sensitivity for predicting lymph node metastases were 0.835, 70.4%, and 78.9% at RNA expression level in the training group, and 0.681, 73.2%, and 75.7% at RNA expression level in the validation group as shown as in result part."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The combined DDX49, EGFR, and T-stage model showed an AUC of 0.835 in the training group and 0.681 in the validation group for predicting lymph node metastases.", "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:37096455"], "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:GSE30219"], "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:GSE30219"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:37096455", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1111/1759-7714.14892", "sha256": "sha256:2d2d441cd8bf7f326cf4432b4f200469628434b3b7d7ea4a9324d32a0b62126f", "bytes": 30411, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1111/1759-7714.14892", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC10234778", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE30219", "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=GSE30219", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE30219", "version": null, "note": "Data and materials will be shared.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", 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