A trans-omics gene-smoking interaction study of lung cancer based on consortium data

肺癌 医学 肿瘤科 癌症 生物信息学 计算生物学 内科学 梅德林 临床试验 呼吸道疾病 风险评估 重症监护医学 肺病
作者
Ning Xie,Xiaoping Xu,Yanru Wang,Anpeng Wang,Xiang Wang,Xuan Wang,Mengshen Zhao,Jiacheng Zhou,Yongyue Wei,Manel Esteller,Zhibin Hu,H. Shen,Rayjean J Hung,Christopher I Amos,Yi Li,David C Christiani,Feng Chen,Yang Zhao,Ruyang Zhang
出处
期刊:American Journal of Respiratory and Critical Care Medicine [American Thoracic Society]
标识
DOI:10.1093/ajrccm/aamaf097
摘要

RATIONALE: Genetically predicted molecular traits provide a cost-effective approach for identifying biomarkers and uncovering underlying biological mechanisms. We extended this framework to investigate gene-smoking interactions in lung cancer susceptibility. OBJECTIVES: To identify trans-omics gene-smoking interactions affecting lung cancer risk and to assess how biomarkers modify effect of smoking. METHODS: We conducted the first trans-omics gene-smoking interaction study of lung cancer by integrating consortium-scale individual genotype data (27,737 cases vs 449,910 non-cases) from the International Lung Cancer OncoArray Consortium (ILCCO-OncoArray), Transdisciplinary Research Into Cancer of the Lung (TRICL), Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO), and the UK Biobank (UKB) with alliance-based summary-level molecular quantitative trait loci (xQTL) data, involving DNA methylation, gene expression, protein, and metabolite. Based on the identified biomarkers, we developed a molecular modifying score (MMS) to delineate gene-smoking interaction patterns and stratify high-risk smokers of lung cancer. MEASUREMENTS AND MAIN RESULTS: Eight biomarkers showing significant interactions with smoking were identified through a two-phase analytic strategy, comprising CpG sites in the nicotinic acetylcholine receptor region and gene RP11-326C3.14. The MMS, constructed by integrating these biomarkers with their effect estimates derived from meta-analysis of all available datasets, effectively stratified lung cancer risk among smokers. Trans-omics integrative analysis revealed functional relationships across molecular layers, particularly implicating the NELFE gene in smoking-related carcinogenesis pathways. CONCLUSIONS: The xWAS framework enables systematic discovery of trans-omics gene-environment interactions. The MMS effectively delineates the patterns of the interaction effects and facilitates risk stratification. Additionally, we launched a free online platform, LungCancer-xWAS-GxE (http://bigdata.njmu.edu.cn/LungCancer-xWAS-GxE/).
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