首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Smoking related carcinogen-DNA adducts in biopsy samples of human urinary bladder: identification of N-(deoxyguanosin-8-yl)-4-aminobiphenyl as a major adduct.
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Smoking related carcinogen-DNA adducts in biopsy samples of human urinary bladder: identification of N-(deoxyguanosin-8-yl)-4-aminobiphenyl as a major adduct.

机译:人膀​​胱活检样本中与吸烟相关的致癌物-DNA加合物:N-(脱氧鸟苷-8-基)-4-氨基联苯的鉴定为主要加合物。

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摘要

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.
机译:通过32P后标记方法研究了42种人膀胱活检样品中共价修饰DNA(致癌物-DNA加合物)的普遍性,并通过核酸酶P1处理和1-丁醇萃取增强了共价修饰。在13位目前吸烟者的DNA样本中,总平均致癌物-DNA加合物水平和几种特定加合物的平均水平显着升高,而从未吸烟者或20位戒烟者(戒烟5年)明显相反。后两组之间没有显着差异。经核酸酶P1处理增强的几种DNA加合物在色谱上类似于先前报道的从吸烟者那里获得的胎盘和肺部DNA样品中推测的烃类DNA加合物。通过1-丁醇萃取检测到假定的芳香胺加合物,当用核酸酶P1处理样品时不存在。其中一种显示出的色谱行为与香烟中存在的人膀胱致癌物4-氨基联苯诱导的主要加合物相同。该加合物在几个具有合成的N-(脱氧鸟苷-8-基)-4-氨基[2,2'-3H]联苯-3',5'-双磷酸酯标记的薄层色谱系统中发生。此外,当从数个个体的薄层色谱图中洗脱该加合物并将其注入HPLC系统时,人膀胱DNA样品中的32P与synthetic化的合成N-(脱氧鸟苷-8-基)- 4-氨基联苯标记。这些数据加强了吸烟与DNA损伤之间的联系,并提出了通过吸烟引发人类膀胱癌的分子基础。

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