Hecht Stephen S
Masonic Cancer Center, University of Minnesota , Minneapolis, Minnesota 55455, United States.
Chem Res Toxicol. 2017 Jan 17;30(1):367-375. doi: 10.1021/acs.chemrestox.6b00372. Epub 2016 Dec 1.
This perspective considers the use of oral cell DNA adducts, together with exposure and genetic information, to potentially identify those cigarette smokers at highest risk for lung cancer, so that appropriate preventive measures could be initiated at a relatively young age before too much damage has been done. There are now well established and validated analytical methods for the quantitation of urinary and serum metabolites of tobacco smoke toxicants and carcinogens. These metabolites provide a profile of exposure and in some cases lung cancer risk, but they do not yield information on the critical DNA damage parameter that leads to mutations in cancer growth control genes such as KRAS and TP53. Studies demonstrate a correlation between changes in the oral cavity and lung in cigarette smokers, due to the field effect of tobacco smoke. Oral cell DNA is readily obtained in contrast to DNA samples from the lung. Studies in which oral cell DNA and salivary DNA have been analyzed for specific DNA adducts are reviewed; some of the adducts identified have also been previously reported in lung DNA from smokers. The multiple challenges of developing a panel of oral cell DNA adducts that could be routinely quantified by mass spectrometry are discussed.
这一观点考虑利用口腔细胞DNA加合物,结合暴露情况和遗传信息,来潜在地识别出肺癌风险最高的吸烟者,以便在造成过多损害之前,在相对年轻的时候就采取适当的预防措施。目前,对于烟草烟雾毒物和致癌物的尿液及血清代谢物的定量分析,已有完善且经过验证的分析方法。这些代谢物可提供暴露情况的概况,在某些情况下还能反映肺癌风险,但它们无法提供导致癌症生长控制基因(如KRAS和TP53)发生突变的关键DNA损伤参数的信息。研究表明,由于烟草烟雾的场效应,吸烟者口腔和肺部之间存在变化相关性。与从肺部获取的DNA样本相比,口腔细胞DNA很容易获得。本文综述了对口腔细胞DNA和唾液DNA进行特定DNA加合物分析的研究;其中一些鉴定出的加合物此前也曾在吸烟者的肺部DNA中报道过。本文还讨论了开发一组可通过质谱法进行常规定量的口腔细胞DNA加合物所面临的多重挑战。