Evidence map›Paper›PMID 41606524›Full record

ArticleBMC cancer2026

Genome-wide DNA methylation profiling reveals body mass Index-dependent epigenetic signatures associated with lung cancer susceptibility.

Zhenzhe Li, Xiao Gao, Qingwei Wang, Zhengqin Zhao

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Article in BMC cancer, 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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5 · Who and what money

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4 authors.

Zhenzhe LiDepartment of Neurosurgery, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, China.
Xiao GaoInstitute of respiratory diseases, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, China.
Qingwei WangDepartment of Hepatobiliary Surgery, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, China.
Zhengqin ZhaoDepartment of Nuclear Medicine, Affiliated Hospital of Guangdong Medical University, No. 57 Renmin Avenue South, Xiashan District, Zhanjiang City, 524000, China. zhaozhengqin62@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to investigate the association between body mass index (BMI)-related DNA methylation alterations and lung cancer risk.

methodsWe conducted a case–control study involving 250 patients with lung cancer and 250 healthy controls. The Illumina 450 K methylation array was used to assess DNA methylation levels in peripheral blood samples. Multivariate logistic regression analysis was performed. Gene Ontology and pathway enrichment analyses were conducted to explore the biological functions of related genes.

resultsAmong the 15,000 CpG sites that passed quality control, 1,200 sites showed significant correlation with BMI. We identified 15 CpG sites as being significantly associated with lung cancer risk, with the most significant being hypermethylation of PARK2 (cg00012345; odds ratio [OR] = 2.5, 95% confidence interval [CI]: 1.7–3.6) and hypomethylation of TP53 (cg04236487; OR = 1.8, 95%CI: 1.3–2.5). Moreover, BMI stratification analysis revealed stronger associations between DNA methylation and lung cancer risk in overweight and obese groups, with PARK2 methylation showing increased risk in the overweight group (OR = 2.2, 95%CI: 1.6–3.0) and ADIPOQ methylation in the obese group (OR = 1.8, 95%CI: 1.3–2.5). Pathway analysis identified significant enrichment in p53 signalling, MAPK signalling, apoptosis and immune response pathways (p < 0.05). The associations of PARK2 and TP53 methylation with lung cancer risk were confirmed in two independent validation cohorts with similar effect sizes.

conclusionsThis study provides the first systematic evidence for the key role of BMI-related DNA methylation alterations in lung cancer development, particularly in overweight and obese populations. Methylation changes in genes may serve as potential biomarkers for lung cancer risk prediction, offering new strategies for early screening and prevention of lung cancer.

Indexed as

Body Mass IndexDNA MethylationEpigenesis, GeneticGenetic Predisposition to DiseaseLung NeoplasmsAgedBiomarkers, TumorCase-Control StudiesCpG IslandsFemaleGenome-Wide Association StudyHumansMaleMiddle AgedObesityRisk FactorsBiomarkers, Tumorparkin proteinTumor Suppressor Protein p53Ubiquitin-Protein LigasesBiomarkersBody mass indexDNA methylationEpigeneticsLung cancerPARK2Risk predictionTP53

Identifiers

PMID41606524
PMCPMC12924305

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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.