Talaska G, al-Juburi A Z, Kadlubar F F
National Center for Toxicological Research, Jefferson, AR 72079.
Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5350-4. doi: 10.1073/pnas.88.12.5350.
The prevalence of covalent modifications to DNA (carcinogen-DNA adducts) in 42 human urinary bladder biopsy samples was investigated by 32P-postlabeling methods, with enhancement by both nuclease P1 treatment and 1-butanol extraction. Total mean carcinogen-DNA adduct levels and the mean levels of several specific adducts were significantly elevated in DNA samples of 13 current smokers, as opposed to 9 never smokers or 20 ex-smokers (5 years abstinence). There was no significant difference between the latter two groups. Several DNA adducts enhanced by nuclease P1 treatment were chromatographically similar to putative hydrocarbon DNA adducts reported earlier for placenta and lung DNA samples obtained from cigarette smokers. Putative aromatic amine adducts were detected by 1-butanol extraction that were not present when the samples were treated with nuclease P1. One of these displayed chromatographic behavior identical to the predominant adduct induced by the human urinary bladder carcinogen, 4-aminobiphenyl, which is present in cigarette smoke. This adduct comigrated in several thin-layer chromatographic systems with a synthetic N-(deoxyguanosin-8-yl)-4-amino[2,2'-3H]biphenyl-3',5'-bisphosphate marker. Moreover, when this adduct was eluted from the thin-layer chromatograms of several individuals and injected onto an HPLC system, the 32P from the human bladder DNA samples coeluted in the same fraction as the tritiated synthetic N-(deoxyguanosin-8-yl)-4-aminobiphenyl marker. These data reinforce an association between cigarette smoking and DNA damage and suggest a molecular basis for the initiation of human urinary bladder cancer by cigarette smoke.
采用³²P后标记法,通过核酸酶P1处理和1-丁醇萃取增强效果,对42份人膀胱活检样本中DNA的共价修饰(致癌物-DNA加合物)发生率进行了研究。13名当前吸烟者的DNA样本中,总平均致癌物-DNA加合物水平以及几种特定加合物的平均水平显著升高,与之形成对比的是9名从不吸烟者和20名已戒烟者(戒烟5年)。后两组之间无显著差异。经核酸酶P1处理增强的几种DNA加合物,在色谱上与先前报道的从吸烟者获得的胎盘和肺DNA样本中的推定烃类DNA加合物相似。通过1-丁醇萃取检测到推定的芳香胺加合物,而在样本经核酸酶P1处理时不存在。其中一种加合物的色谱行为与人类膀胱致癌物4-氨基联苯诱导的主要加合物相同,4-氨基联苯存在于香烟烟雾中。这种加合物在几个薄层色谱系统中与合成的N-(脱氧鸟苷-8-基)-4-氨基[2,2'-³H]联苯-3',5'-双磷酸标记物共迁移。此外,当从几个人的薄层色谱图中洗脱这种加合物并注入高效液相色谱系统时,人膀胱DNA样本中的³²P与氚标记的合成N-(脱氧鸟苷-8-基)-4-氨基联苯标记物在同一馏分中共洗脱。这些数据加强了吸烟与DNA损伤之间的关联,并提示了香烟烟雾引发人类膀胱癌的分子基础。