Fu Peter P
National Center for Toxicological Research, U.S. Food and Drug Administration , Jefferson, Arkansas 72079, United States.
Chem Res Toxicol. 2017 Jan 17;30(1):81-93. doi: 10.1021/acs.chemrestox.6b00297. Epub 2016 Nov 21.
Pyrrolizidine alkaloids (PAs) and PA N-oxides are a class of phytochemical carcinogens contained in over 6000 plant species spread around the world. It has been estimated that approximately half of the 660 PAs and PA N-oxides that have been characterized are cytotoxic, genotoxic, and tumorigenic. It was recently determined that a genotoxic mechanism of liver tumor initiation mediated by PA-derived DNA adducts is a common metabolic activation pathway of a number of PAs. We proposed this set of PA-derived DNA adducts could be a common biological biomarker of PA exposure and a potential biomarker of PA-induced liver tumor formation. We have also found that several reactive secondary pyrrolic metabolites can dissociate and interconvert to other secondary pyrrolic metabolites, resulting in the formation of the same exogenous DNA adducts. This present perspective reports the current progress on these new findings and proposes future research needed for obtaining a greater understanding of the role of this activation pathway and validating the use of this set of PA-derived DNA adducts as a biological biomarker of PA-induced liver tumor initiation.
吡咯里西啶生物碱(PAs)和PA N-氧化物是一类植物化学致癌物,存在于全球6000多种植物中。据估计,已被鉴定的660种PAs和PA N-氧化物中约有一半具有细胞毒性、基因毒性和致瘤性。最近确定,由PA衍生的DNA加合物介导的肝肿瘤起始的基因毒性机制是多种PAs常见的代谢激活途径。我们提出,这组PA衍生的DNA加合物可能是PA暴露的常见生物标志物以及PA诱导肝肿瘤形成的潜在生物标志物。我们还发现,几种具有反应活性的二级吡咯代谢产物可以解离并相互转化为其他二级吡咯代谢产物,从而形成相同的外源性DNA加合物。本综述报告了这些新发现的当前进展,并提出了未来研究的需求,以便更深入地了解这一激活途径的作用,并验证将这组PA衍生的DNA加合物用作PA诱导肝肿瘤起始的生物标志物的用途。