AHRR methylation in heavy smokers: associations with smoking, lung cancer risk, and lung cancer mortality

被引:27
|
作者
Grieshober, Laurie [1 ]
Graw, Stefan [2 ,3 ]
Barnett, Matt J. [4 ]
Thornquist, Mark D. [4 ]
Goodman, Gary E. [4 ]
Chen, Chu [4 ,5 ,6 ]
Koestler, Devin C. [2 ]
Marsit, Carmen J. [3 ]
Doherty, Jennifer A. [1 ,4 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Dept Populat Hlth Sci, 2000 Circle Hope Dr,Room 4746, Salt Lake City, UT 84112 USA
[2] Univ Kansas, Med Ctr, Dept Biostat & Data Sci, Kansas City, KS 66103 USA
[3] Emory Univ, Rollins Sch Publ Hlth, Dept Environm Hlth, Atlanta, GA 30322 USA
[4] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Program Epidemiol, 1124 Columbia St, Seattle, WA 98104 USA
[5] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98195 USA
[6] Univ Washington, Sch Med, Dept Otolaryngol Head & Neck Surg, Seattle, WA USA
关键词
Lung cancer; Epidemiology; Biomarkers; serum biomarkers; Methylation; AHRR; CARET; Mortality; ARYL-HYDROCARBON RECEPTOR; DNA METHYLATION; BETA-CAROTENE; PERIPHERAL-BLOOD; COMBINATION; SIGNATURES; EXPOSURE; GENES;
D O I
10.1186/s12885-020-07407-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundA low level of methylation at cg05575921 in the aryl-hydrocarbon receptor repressor (AHRR) gene is robustly associated with smoking, and some studies have observed associations between cg05575921 methylation and increased lung cancer risk and mortality. To prospectively examine whether decreased methylation at cg05575921 may identify high risk subpopulations for lung cancer screening among heavy smokers, and mortality in cases, we evaluated associations between cg05575921 methylation and lung cancer risk and mortality, by histotype, in heavy smokers.MethodsThe beta -Carotene and Retinol Efficacy Trial (CARET) included enrollees ages 45-69 with >= 20 pack-year smoking histories and/or occupational asbestos exposure. A subset of CARET participants had cg05575921 methylation available from HumanMethylationEPIC assays of blood collected on average 4.3years prior to lung cancer diagnosis in cases. Cg05575921 methylation beta -values were treated continuously for a 10% methylation decrease and as quintiles, where quintile 1 (Q1, referent) represents high methylation and Q5, low methylation. We used conditional logistic regression models to examine lung cancer risk overall and by histotype in a nested case-control study including 316 lung cancer cases (diagnosed through 2005) and 316 lung cancer-free controls matched on age (5years), sex, race/ethnicity, enrollment year, current/former smoking, asbestos exposure, and follow-up time. Mortality analyses included 372 lung cancer cases diagnosed between 1985 and 2013 with available methylation data. We used Cox proportional hazards models to examine mortality overall and by histotype.ResultsDecreased cg05575921 methylation was strongly associated with smoking, even in our population of heavy smokers. We did not observe associations between decreased pre-diagnosis cg05575921 methylation and increased lung cancer risk, overall or by histotype. We observed linear increasing trends for lung cancer-specific mortality across decreasing cg05575921 methylation quintiles for adenocarcinoma and small cell carcinoma (P-trends=0.01 and 0.04, respectively).Conclusions In our study of heavy smokers, decreased cg05575921 methylation was strongly associated with smoking but not increased lung cancer risk. The observed association between cg05575921 methylation and increased mortality in adenocarcinoma and small cell histotypes requires further examination. Our results do not support using decreased cg05575921 methylation as a biomarker for lung cancer screening risk stratification.
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页数:10
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