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[13C]标记的烟草烟雾与DNA的反应,以生成无需代谢活化即可形成的特定加合物。

Reactions of [13C]-labelled tobacco smoke with DNA to generate selected adducts formed without metabolic activation.

作者信息

Tang Mei-Kuen, Ostlund Trevor, Dameh Nour F, Alcheva Aleksandra, Cohen Jerry D, Hegeman Adrian D, Carmella Steven G, Stepanov Irina, Hecht Stephen S

机构信息

Masonic Cancer Center, University of Minnesota, 420 Delaware Street Southeast, Minneapolis, MN 55455, United States.

Graduate Program in Molecular Pharmacology and Therapeutics, University of Minnesota, 321 Chruch Street Southeast, Minneapolis, MN 55455, United States.

出版信息

Carcinogenesis. 2025 Apr 3;46(2). doi: 10.1093/carcin/bgaf008.

Abstract

DNA adducts are central in the carcinogenic process because they can cause miscoding leading to permanent mutations in important genes involved in carcinogenesis. While it is known that tobacco smoking leads to increased levels of multiple DNA adducts, most DNA adducts detected to date in humans cannot be explicitly attributed to smoking but instead have various possible exogenous and endogenous sources. We plan to probe the tobacco source of DNA adducts by providing carbon-13 labelled ([13C]-labelled) cigarettes to smokers and analyzing [13C]-labelled DNA adducts in their oral cells to determine which adducts arise from smoking. Prior to conducting studies in humans, we first report here proof-of-principle machine smoking experiments to evaluate carbon isotopologues of (a) selected carbonyls and (b) DNA adducts resulting from direct exposure of cigarette smoke vapour-phase to calf-thymus DNA. The smoke of the study cigarettes, made from a 50:50 mixture of [13C]-labelled tobacco and a popular commercial tobacco, yielded similar concentrations of carbonyl compounds and their respective DNA adducts compared with the smoke of 1R6F reference cigarettes and the popular brand of cigarettes. We detected [13C]-isotopologues of DNA adducts such as 1,N6-etheno-dA, (8R/S)-3-(2'-deoxyribos-1-yl)-5,6,7,8-tetrahydro-8-hydroxypyrimido[1,2-a]purine-10(3H)-one (γ-OH-Acr-dG), and (6S,8S and 6R,8R)-3-(2'-deoxyribos-1-yl)-5,6,7,8-tetrahydro-8-hydroxy-6-methylpyrimido[1,2-a]purine-10(3H)-one [(6S,8S)-γ-OH-Cro-dG and (6R,8R)-γ-OH-Cro-dG], proving that they have a direct source from tobacco smoke and providing important new insights regarding their mechanisms of formation. These unique results form the basis for further studies in cell culture and in cigarette smokers to establish how carcinogens in tobacco smoke cause DNA adduct formation.

摘要

DNA加合物在致癌过程中起着核心作用,因为它们可导致错配,进而在参与致癌作用的重要基因中引发永久性突变。虽然已知吸烟会导致多种DNA加合物水平升高,但迄今为止在人类中检测到的大多数DNA加合物不能明确归因于吸烟,而是有各种可能的外源性和内源性来源。我们计划通过向吸烟者提供碳-13标记([13C]标记)的香烟,并分析他们口腔细胞中的[13C]标记DNA加合物,来探究DNA加合物的烟草来源,以确定哪些加合物源自吸烟。在对人类进行研究之前,我们在此首先报告原理验证机器吸烟实验,以评估(a)选定羰基化合物的碳同位素异构体,以及(b)香烟烟雾气相直接暴露于小牛胸腺DNA所产生的DNA加合物的碳同位素异构体。由[13C]标记烟草和一种流行商业烟草按50:50比例混合制成的研究香烟所产生的烟雾,与1R6F参考香烟和流行品牌香烟的烟雾相比,产生的羰基化合物及其各自的DNA加合物浓度相似。我们检测到了DNA加合物的[13C]同位素异构体,如1,N6-乙烯基-dA、(8R/S)-3-(2'-脱氧核糖-1-基)-5,6,7,8-四氢-8-羟基嘧啶并[1,2-a]嘌呤-10(3H)-酮(γ-OH-Acr-dG),以及(6S,8S和6R,8R)-3-(2'-脱氧核糖-1-基)-5,6,7,8-四氢-8-羟基-6-甲基嘧啶并[1,2-a]嘌呤-10(3H)-酮[(6S,8S)-γ-OH-Cro-dG和(6R,8R)-γ-OH-Cro-dG],证明它们直接来源于烟草烟雾,并为其形成机制提供了重要的新见解。这些独特的结果为进一步开展细胞培养研究和对吸烟者的研究奠定了基础,以确定烟草烟雾中的致癌物如何导致DNA加合物的形成。

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