Stephen B Stanfill, Stephen S Hecht, Andreas C Joerger, Pablo J González, Luisa B Maia, Maria G Rivas, José J G Moura, Alpana K Gupta, Nick E Le Brun, Jason C Crack, Pierre Hainaut, Courtney Sparacino-Watkins, Robert E Tyx, Suresh D Pillai, Ghazi S Zaatari, S Jane Henley, Benjamin C Blount, Clifford H Watson, Bernd Kaina, Ravi Mehrotra
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This review covers the series of biochemical and chemical transformations, related to TSNAs, leading from tobacco cultivation to cancer initiation. A key aim of this review is to provide a greater understanding of TSNAs: their precursors, the microbial and chemical mechanisms that contribute to their formation in ST, their mutagenicity leading to cancer due to ST use, and potential means of lowering TSNA levels in tobacco products. TSNAs are not present in harvested tobacco but can form due to nitrosating agents reacting with tobacco alkaloids present in tobacco during certain types of curing. TSNAs can also form during or following ST production when certain microorganisms perform nitrate metabolism, with dissimilatory nitrate reductases converting nitrate to nitrite that is then released into tobacco and reacts chemically with tobacco alkaloids. When ST usage occurs, TSNAs are absorbed and metabolized to reactive compounds that form DNA adducts leading to mutations in critical target genes, including the <i>RAS</i> oncogenes and the p53 tumor suppressor gene. DNA repair mechanisms remove most adducts induced by carcinogens, thus preventing many but not all mutations. Lastly, because TSNAs and other agents cause cancer, previously documented strategies for lowering their levels in ST products are discussed, including using tobacco with lower nornicotine levels, pasteurization and other means of eliminating microorganisms, omitting fermentation and fire-curing, refrigerating ST products, and including nitrite scavenging chemicals as ST ingredients.</p>","PeriodicalId":10869,"journal":{"name":"Critical Reviews in Toxicology","volume":" ","pages":"658-701"},"PeriodicalIF":5.7000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"From cultivation to cancer: formation of <i>N</i>-nitrosamines and other carcinogens in smokeless tobacco and their mutagenic implications.\",\"authors\":\"Stephen B Stanfill, Stephen S Hecht, Andreas C Joerger, Pablo J González, Luisa B Maia, Maria G Rivas, José J G Moura, Alpana K Gupta, Nick E Le Brun, Jason C Crack, Pierre Hainaut, Courtney Sparacino-Watkins, Robert E Tyx, Suresh D Pillai, Ghazi S Zaatari, S Jane Henley, Benjamin C Blount, Clifford H Watson, Bernd Kaina, Ravi Mehrotra\",\"doi\":\"10.1080/10408444.2023.2264327\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Tobacco use is a major cause of preventable morbidity and mortality globally. 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引用次数: 0
摘要
烟草使用是全球可预防的发病和死亡的主要原因。包括无烟烟草(ST)在内的烟草制品通常含有烟草特有的 N-亚硝胺(TSNAs),如 N'-亚硝基烟碱(NNN)和 4-(甲基亚硝基氨基)-1-(3-吡啶基)-丁酮(NNK),这些物质是强致癌物,会导致人类 DNA 中的关键基因发生突变。本综述涵盖了从烟草种植到引发癌症的一系列与 TSNA 有关的生化转化过程。本综述的一个主要目的是加深对 TSNA 的了解:TSNA 的前体、促使其在 ST 中形成的微生物和化学机制、因使用 ST 而导致癌症的致突变性,以及降低烟草产品中 TSNA 含量的潜在方法。TSNA 不存在于采收的烟草中,但在某些类型的腌制过程中,亚硝酸化剂与烟草中的烟草生物碱发生反应会形成 TSNA。某些微生物在进行硝酸盐代谢时,会将硝酸盐转化为亚硝酸盐,然后释放到烟草中并与烟草生物碱发生化学反应。当使用 ST 时,TSNA 被吸收并代谢为活性化合物,形成 DNA 加合物,导致关键靶基因突变,包括 RAS 致癌基因和 p53 抑癌基因。DNA 修复机制可清除致癌物质诱导的大多数加合物,从而防止许多但并非所有基因突变。最后,由于 TSNAs 和其他致癌物质会致癌,我们讨论了以前记录的降低 ST 产品中 TSNAs 和其他致癌物质含量的策略,包括使用烟草中烟碱含量较低的烟草、巴氏杀菌和其他消除微生物的方法、避免发酵和火腌制、冷藏 ST 产品以及将亚硝酸盐清除化学物作为 ST 成分。
From cultivation to cancer: formation of N-nitrosamines and other carcinogens in smokeless tobacco and their mutagenic implications.
Tobacco use is a major cause of preventable morbidity and mortality globally. Tobacco products, including smokeless tobacco (ST), generally contain tobacco-specific N-nitrosamines (TSNAs), such as N'-nitrosonornicotine (NNN) and 4-(methylnitrosamino)-1-(3-pyridyl)-butanone (NNK), which are potent carcinogens that cause mutations in critical genes in human DNA. This review covers the series of biochemical and chemical transformations, related to TSNAs, leading from tobacco cultivation to cancer initiation. A key aim of this review is to provide a greater understanding of TSNAs: their precursors, the microbial and chemical mechanisms that contribute to their formation in ST, their mutagenicity leading to cancer due to ST use, and potential means of lowering TSNA levels in tobacco products. TSNAs are not present in harvested tobacco but can form due to nitrosating agents reacting with tobacco alkaloids present in tobacco during certain types of curing. TSNAs can also form during or following ST production when certain microorganisms perform nitrate metabolism, with dissimilatory nitrate reductases converting nitrate to nitrite that is then released into tobacco and reacts chemically with tobacco alkaloids. When ST usage occurs, TSNAs are absorbed and metabolized to reactive compounds that form DNA adducts leading to mutations in critical target genes, including the RAS oncogenes and the p53 tumor suppressor gene. DNA repair mechanisms remove most adducts induced by carcinogens, thus preventing many but not all mutations. Lastly, because TSNAs and other agents cause cancer, previously documented strategies for lowering their levels in ST products are discussed, including using tobacco with lower nornicotine levels, pasteurization and other means of eliminating microorganisms, omitting fermentation and fire-curing, refrigerating ST products, and including nitrite scavenging chemicals as ST ingredients.
期刊介绍:
Critical Reviews in Toxicology provides up-to-date, objective analyses of topics related to the mechanisms of action, responses, and assessment of health risks due to toxicant exposure. The journal publishes critical, comprehensive reviews of research findings in toxicology and the application of toxicological information in assessing human health hazards and risks. Toxicants of concern include commodity and specialty chemicals such as formaldehyde, acrylonitrile, and pesticides; pharmaceutical agents of all types; consumer products such as macronutrients and food additives; environmental agents such as ambient ozone; and occupational exposures such as asbestos and benzene.