Evidence map›Paper›PMID 40939066›Full record

ArticleCancer biomarkers : section A of Disease markers2025

Machine learning-driven gene expression profiling for lung cancer stage determination.

Yinbo Wang, Kai Fu

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Yinbo WangDepartment of Biostatistics, University of Michigan-Ann Arbor, Ann Arbor, MI, USA.ORCID 0009-0008-2893-491X
Kai FuDepartment of Molecular, Cellular and Developmental Bology, University of California Los Angeles, Los Angeles, CA, USA.ORCID 0000-0002-8107-3556

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundLung cancer remains a leading cause of cancer-related mortality, with accurate staging essential for guiding treatment. Advances in next-generation sequencing (NGS) and machine learning (ML) enable more precise classification, improving on traditional imaging-based methods.ObjectiveThis retrospective study applies XGBoost with cross-validation (CV) to classify early vs. late-stage lung cancer using RNA-Seq data from 993 patients in The Cancer Genome Atlas (TCGA) cohort.MethodsGene selection was conducted using the Wilcoxon rank-sum test on training data, and the XGBoost model was optimized via cross-validation. Model performance was assessed using the Area Under the Curve (AUC), with sensitivity-specificity analysis across classification thresholds.ResultsThe XGBoost model achieved a test AUC of 0.6534, identifying 40 key genes that optimize predictive accuracy while minimizing overfitting. Thresholds of 0.3 and 0.4 were optimal, balancing sensitivity and specificity for clinical application

Indexed as

Gene Expression ProfilingLung NeoplasmsMachine LearningAdenocarcinoma of LungAdultAgedAged, 80 and overBoosting Machine Learning AlgorithmsCarcinoma, Squamous CellCohort StudiesHumansMiddle AgedRetrospective Studiescancer staginggene expressionLung cancermachine learningRNA-SeqXGBoost

Identifiers

PMID40939066
PMCPMC13085915

What Socratic holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.