Peterson L A, Naruko K C, Predecki D P
Division of Environmental and Occupational Health and Cancer Center, University of Minnesota, Minneapolis 55455, USA.
Chem Res Toxicol. 2000 Jul;13(7):531-4. doi: 10.1021/tx000065f.
Furan is classified as a nongenotoxic hepatocarcinogen. It is thought to be activated to a toxic metabolite, cis-2-butene-1,4-dial, which is acutely toxic to liver cells. The resulting cytotoxicity is followed by compensatory cell proliferation, increasing the likelihood of tumor production. We examined the genotoxic activity of cis-2-butene-1,4-dial in several strains of Salmonella typhimurium commonly used in the Ames assay. This reactive compound tested positive in TA104, a strain that is sensitive to aldehydes. Mutagenic activity was concentration-dependent (1000 +/- 180 revertants/micromol). Incubation of cis-2-butene-1,4-dial with glutathione prior to addition of bacteria inhibited both the acute toxic and genotoxic activity of this compound. No evidence of mutagenic activity was seen at nontoxic concentrations in TA97, TA98, TA100, and TA102. Our findings are consistent with the hypothesis that cis-2-butene-1,4-dial reacts with DNA to form mutagenic adducts. Our data suggest that cis-2-butene-1,4-dial may be an important genotoxic as well as toxic intermediate in furan-induced tumorigenesis.
呋喃被归类为非遗传毒性肝癌致癌物。它被认为会被激活形成一种有毒代谢物,顺式-2-丁烯-1,4-二醛,这种物质对肝细胞具有急性毒性。由此产生的细胞毒性之后会伴随代偿性细胞增殖,增加肿瘤产生的可能性。我们检测了顺式-2-丁烯-1,4-二醛在艾姆斯试验中常用的几种鼠伤寒沙门氏菌菌株中的遗传毒性活性。这种反应性化合物在对醛敏感的TA104菌株中检测呈阳性。诱变活性呈浓度依赖性(1000±180回复突变体/微摩尔)。在加入细菌之前,将顺式-2-丁烯-1,4-二醛与谷胱甘肽一起孵育可抑制该化合物的急性毒性和遗传毒性活性。在TA97、TA98、TA100和TA102的无毒浓度下未观察到诱变活性的证据。我们的研究结果与顺式-2-丁烯-1,4-二醛与DNA反应形成诱变加合物的假设一致。我们的数据表明,顺式-2-丁烯-1,4-二醛可能是呋喃诱导肿瘤发生过程中一种重要的遗传毒性以及毒性中间体。