Urinary levels of cigarette smoke constituent metabolites are prospectively associated with lung cancer development in smokers

Jian-Min Yuan, Yu-Tang Gao, Sharon E Murphy, Steven G Carmella, Renwei Wang, Yan Zhong, Kristin A Moy, Andrew B Davis, Li Tao, Menglan Chen, Shaomei Han, Heather H Nelson, Mimi C Yu, Stephen S Hecht, Jian-Min Yuan, Yu-Tang Gao, Sharon E Murphy, Steven G Carmella, Renwei Wang, Yan Zhong, Kristin A Moy, Andrew B Davis, Li Tao, Menglan Chen, Shaomei Han, Heather H Nelson, Mimi C Yu, Stephen S Hecht

Abstract

Polycyclic aromatic hydrocarbons (PAH) are believed to be among the principal causative agents for lung cancer in smokers, but no epidemiologic studies have evaluated the relationship of PAH uptake and metabolism to lung cancer. In this study, we quantified prediagnostic urinary levels of r-1,t-2,3,c-4-tetrahydroxy-1,2,3,4-tetrahydrophenanthrene (PheT), a validated biomarker of PAH uptake and metabolism, as well as 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol and its glucuronides (total NNAL), and cotinine and its glucuronides (total cotinine), validated biomarkers of uptake of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, and nicotine, respectively, in relation to lung cancer risk among current smokers in a nested case-control study within a cohort of 18,244 Chinese men in Shanghai, China. Urinary levels of PheT, total NNAL, and total cotinine were significantly higher in cases than controls (N = 476 matched pairs). ORs (95% confidence intervals) for lung cancer in the second, third, fourth, and fifth quintiles of PheT were 1.70 (1.00-2.88), 1.07 (0.62-1.84), 1.48 (0.86-2.53), and 2.34 (1.33-4.11), respectively, relative to the lowest quartile (P(trend) = 0.023) after adjustment for self-reported smoking intensity and duration and urinary total NNAL and total cotinine. This study also confirmed that urinary total NNAL and total cotinine are independently related to lung cancer risk.

Conflict of interest statement

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

©2011 AACR.

Source: PubMed

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