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Genome-wide gene–smoking interaction study identified novel susceptibility loci for non-small cell lung cancer in Chinese populations.

Authors :
Wang, Yuzhuo
Ji, Mengmeng
Zhu, Meng
Fan, Jingyi
Xie, Junxing
Huang, Yanqian
Wei, Xiaoxia
Jiang, Xiangxiang
Xu, Jing
Chen, Liang
Yin, Rong
Wang, Cheng
Zhang, Ruyang
Zhao, Yang
Dai, Juncheng
Jin, Guangfu
Hu, Zhibin
Christiani, David C
Ma, Hongxia
Xu, Lin
Source :
Carcinogenesis; Sep2021, Vol. 42 Issue 9, p1154-1161, 8p
Publication Year :
2021

Abstract

Gene–smoking interactions play important roles in the development of non-small cell lung cancer (NSCLC). To identify single-nucleotide polymorphisms (SNPs) that modify the association of smoking behavior with NSCLC risk, we conducted a genome-wide gene–smoking interaction study in Chinese populations. The genome-wide interaction analysis between SNPs and smoking status (ever- versus never-smokers) was carried out using genome-wide association studies of NSCLC, which included 13 327 cases and 13 328 controls. Stratified analysis by histological subtypes was also conducted. We used a genome-wide significance threshold of 5 × 10<superscript>−8</superscript> for identifying significant gene–smoking interactions and 1 × 10<superscript>–6</superscript> for identifying suggestive results. Functional annotation was performed to identify potential functional SNPs and target genes. We identified three novel loci with significant or suggestive gene–smoking interaction. For NSCLC, the interaction between rs2746087 (20q11.23) and smoking status reached genome-wide significance threshold [odds ratio (OR) = 0.63, 95% confidence interval (CI): 0.54–0.74, P = 3.31 × 10<superscript>–8</superscript>], and the interaction between rs11912498 (22q12.1) and smoking status reached suggestive significance threshold (OR = 0.72, 95% CI: 0.63–0.82, P = 8.10 × 10<superscript>–7</superscript>). Stratified analysis by histological subtypes identified suggestive interactions between rs459724 (5q11.2) and smoking status (OR = 0.61, 95% CI: 0.51–0.73, P = 7.55 × 10<superscript>–8</superscript>) in the risk of lung squamous cell carcinoma. Functional annotation indicated that both classic and novel biological processes, including nicotine addiction and airway clearance, may modulate the susceptibility to NSCLC. These novel loci provide new insights into the biological mechanisms underlying NSCLC risk. Independent replication in large-scale studies is needed and experimental studies are warranted to functionally validate these associations. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01433334
Volume :
42
Issue :
9
Database :
Complementary Index
Journal :
Carcinogenesis
Publication Type :
Academic Journal
Accession number :
152885405
Full Text :
https://doi.org/10.1093/carcin/bgab064