Evidence map›Paper›PMID 42110019›Full record

ArticleCureus2026

DNA Methylation Signatures Associated With Smoking Status Across Lung Cancer Subtypes Using The Cancer Genome Atlas (TCGA) Methylation Data.

Blessing T Ojinna, Abimbola E Arisoyin, Akinyele Oladimeji, Chigozirim Okpechi, Azeberoje Osueni

Abstract read
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Blessing T OjinnaInternal Medicine, Guthrie Lourdes Hospital, Binghamton, USA.
Abimbola E ArisoyinPsychiatry, Harlem Hospital Center, New York, USA.
Akinyele OladimejiFamily Medicine, Obafemi Awolowo University, Ile-Ife, NGA.
Chigozirim OkpechiMedicine, St George's University, St. George's, GRD.
Azeberoje OsueniGastroenterology and Hepatology, Lagos University Teaching Hospital, Lagos, NGA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer remains the leading cause of cancer-related mortality worldwide, with cigarette smoking as its strongest etiologic factor. Beyond genetic mutations, smoking induces epigenetic alterations, particularly DNA methylation, which may differ across lung cancer subtypes and contribute to tumor heterogeneity.

objectiveThe objective of this study was to identify smoking-associated differentially methylated CpG sites (FDR < 0.05) across lung cancer subtypes using The Cancer Genome Atlas (TCGA) 450K methylation data, and to enhance biological interpretation by annotating their genomic context and functional relevance, including associated genes and regulatory features. METHODOLOGY: This retrospective observational study analyzed Illumina HumanMethylation450 BeadChip data from TCGA lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC) cohorts. Multivariable linear models within the limma framework assessed differential methylation between smokers and never smokers, adjusting for age, sex, tumor stage, and histology. False discovery rate (FDR) correction was applied.

resultsA total of 771 patients (92 never smokers, 679 smokers) were analyzed. Seven CpG sites were significantly associated with smoking status (FDR < 0.05), with absolute methylation differences (Δβ) ranging from 0.100 to 0.123. Subtype-specific analyses identified eight LUAD-specific and five LUSC-specific smoking-associated CpG sites. LUAD exhibited both hypermethylation and hypomethylation patterns, whereas LUSC showed predominantly smoking-related hypomethylation.

conclusionSmoking is associated with distinct and subtype-specific DNA methylation signatures in lung cancer, underscoring its role in epigenetic tumor modulation and supporting the potential utility of methylation markers in lung cancer stratification and risk assessment.

Indexed as

dna methylationepigeneticslung cancernon-small cell lung cancersmokingtcga

Identifiers

PMID42110019
PMCPMC13149547

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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 OpenQuestion graph.