Authors' Affiliations: Division of Cancer Control and Population Sciences, University of Pittsburgh Cancer Institute; Department of Epidemiology, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania; and Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Cancer Res. 2014 Jan 15;74(2):401-11. doi: 10.1158/0008-5472.CAN-13-3178. Epub 2014 Jan 9.
Tobacco-constituent biomarkers are metabolites of specific compounds present in tobacco or tobacco smoke. Highly reliable analytic methods, based mainly on mass spectrometry, have been developed for quantitation of these biomarkers in both urine and blood specimens. There is substantial interindividual variation in smoking-related lung cancer risk that is determined in part by individual variability in the uptake and metabolism of tobacco smoke carcinogens. Thus, by incorporating these biomarkers in epidemiologic studies, we can potentially obtain a more valid and precise measure of in vivo carcinogen dose than by using self-reported smoking history, ultimately improving the estimation of smoking-related lung cancer risk. Indeed, we have demonstrated this by using a prospective study design comparing biomarker levels in urine samples collected from smokers many years before their development of cancer versus those in their smoking counterparts without a cancer diagnosis. The following urinary metabolites were associated with lung cancer risk, independent of smoking intensity and duration: cotinine plus its glucuronide, a biomarker of nicotine uptake; 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol and its glucuronides (total NNAL), a biomarker of the tobacco carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK); and r-1-,t-2,3,c-4-tetrahydroxy-1,2,3,4-tetrahydrophenanthrene (PheT), a biomarker of polycyclic aromatic hydrocarbons (PAH). These results provide several possible new directions for using tobacco smoke-constituent biomarkers in lung cancer prevention, including improved lung cancer risk assessment, intermediate outcome determination in prevention trials, and regulation of tobacco products.
烟草成分生物标志物是烟草或烟草烟雾中特定化合物的代谢物。已经开发出了高度可靠的分析方法,主要基于质谱法,用于定量检测尿液和血液样本中的这些生物标志物。吸烟相关肺癌风险存在很大的个体间差异,部分原因是个体对烟草烟雾致癌物的吸收和代谢存在个体差异。因此,通过将这些生物标志物纳入流行病学研究中,我们可以潜在地获得比使用自我报告的吸烟史更有效和更精确的体内致癌物剂量测量,从而最终改善对吸烟相关肺癌风险的估计。事实上,我们通过使用前瞻性研究设计,比较了多年前吸烟者尿液样本中的生物标志物水平与未患癌症的吸烟对照者的水平,证明了这一点。以下尿代谢物与肺癌风险相关,独立于吸烟强度和持续时间:可替宁及其葡萄糖醛酸,尼古丁吸收的生物标志物;4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁醇及其葡萄糖醛酸(总 NNAL),烟草致癌物 4-(甲基亚硝氨基)-1-(3-吡啶基)-1-丁酮(NNK)的生物标志物;和 r-1-,t-2,3,c-4-四羟基-1,2,3,4-四氢菲(PheT),多环芳烃(PAH)的生物标志物。这些结果为使用烟草成分生物标志物预防肺癌提供了几个可能的新方向,包括改善肺癌风险评估、预防试验中的中间结果确定以及烟草产品监管。