Role of nicotine dependence on the relationship between variants in the nicotinic receptor genes and risk of lung adenocarcinoma

Authors

Tung-Sung Tseng, LSU Health Science Center - New OrleansFollow
Jong Y. Park, Department of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, United States of America.
Jovanny Zabaleta, LSU Health Science Center - New OrleansFollow
Sarah Moody-Thomas, LSU Health Science Center - New OrleansFollow
Melinda S. Sothern, LSU Health Science Center - New OrleansFollow
Ted Chen, Tulane University
David E. Evans, H. Lee Moffitt Cancer Center and Research Institute, Tampa
Hui-Yi Lin, H. Lee Moffitt Cancer Center and Research Institute, Tampa

Document Type

Article

Publication Date

1-1-2014

Publication Title

PloS one

Abstract

Several variations in the nicotinic receptor genes have been identified to be associated with both lung cancer risk and smoking in the genome-wide association (GWA) studies. However, the relationships among these three factors (genetic variants, nicotine dependence, and lung cancer) remain unclear. In an attempt to elucidate these relationships, we applied mediation analysis to quantify the impact of nicotine dependence on the association between the nicotinic receptor genetic variants and lung adenocarcinoma risk. We evaluated 23 single nucleotide polymorphisms (SNPs) in the five nicotinic receptor related genes (CHRNB3, CHRNA6, and CHRNA5/A3/B4) previously reported to be associated with lung cancer risk and smoking behavior and 14 SNPs in the four 'control' genes (TERT, CLPTM1L, CYP1A1, and TP53), which were not reported in the smoking GWA studies. A total of 661 lung adenocarcinoma cases and 1,347 controls with a smoking history, obtained from the Environment and Genetics in Lung Cancer Etiology case-control study, were included in the study. Results show that nicotine dependence is a mediator of the association between lung adenocarcinoma and gene variations in the regions of CHRNA5/A3/B4 and accounts for approximately 15% of this relationship. The top two CHRNA3 SNPs associated with the risk for lung adenocarcinoma were rs1051730 and rs12914385 (p-value = 1.9×10(-10) and 1.1×10(-10), respectively). Also, these two SNPs had significant indirect effects on lung adenocarcinoma risk through nicotine dependence (p = 0.003 and 0.007). Gene variations rs2736100 and rs2853676 in TERT and rs401681 and rs31489 in CLPTM1L had significant direct associations on lung adenocarcinoma without indirect effects through nicotine dependence. Our findings suggest that nicotine dependence plays an important role between genetic variants in the CHRNA5/A3/B4 region, especially CHRNA3, and lung adenocarcinoma. This may provide valuable information for understanding the pathogenesis of lung adenocarcinoma and for conducting personalized smoking cessation interventions.

First Page

e107268

PubMed ID

25233467

Volume

9

Issue

9

Creative Commons License

This work is licensed under a Creative Commons Attribution 3.0 License.

Recommended Citation

Tseng, Tung-Sung; Park, Jong Y.; Zabaleta, Jovanny; Moody-Thomas, Sarah; Sothern, Melinda S.; Chen, Ted; Evans, David E.; and Lin, Hui-Yi, "Role of nicotine dependence on the relationship between variants in the nicotinic receptor genes and risk of lung adenocarcinoma" (2014). School of Public Health Faculty Publications. 209.
https://digitalscholar.lsuhsc.edu/soph_facpubs/209