Theumer M G, Henneb Y, Khoury L, Snini S P, Tadrist S, Canlet C, Puel O, Oswald I P, Audebert M
Toxalim, Université de Toulouse, INRA, INP-ENVT, INP-EI-Purpan, Université de Toulouse 3 Paul Sabatier, Toulouse, France.
Toxalim, Université de Toulouse, INRA, INP-ENVT, INP-EI-Purpan, Université de Toulouse 3 Paul Sabatier, Toulouse, France.
Toxicol Lett. 2018 May 1;287:100-107. doi: 10.1016/j.toxlet.2018.02.007. Epub 2018 Feb 5.
Aflatoxins are found as food contaminant and some of them demonstrate a carcinogenic effect. The aflatoxins biosynthetic pathway involves 15 successive steps. The aim of this study was to compare the toxicity of aflatoxins and their precursors in three human cell lines. We tested the four aflatoxins and two of their metabolites; three early metabolic precursors and two late biosynthetic precursors. Cyclopiazonic acid, synthesized in parallel with aflatoxins, was also tested. The cytotoxicity and the genotoxicity was evaluated with the γH2AX assay in three human cell lines with different bioactivation capacities. Our results indicated that the most genotoxic chemicals in the three cell lines were in decreasing order sterigmatocystin (ST), aflatoxin B1 (AFB1), aflatoxicol (AFL), aflatoxin G1 (AFG1) and versicolorin A (VERA). Aflatoxin M1 (AFM1) demonstrated genotoxic property in only one cell line. The other tested compounds did not demonstrate any genotoxic activity. Overall, our results suggested different genotoxic mechanisms of action for the tested compounds, involving specific bioactivation pathways. Moreover, some metabolic precursors of aflatoxins demonstrated genotoxic potential equivalent or greater to AFB1. This should be taking into account for the development of new strategies intended to reduce the aflatoxins exposure and for human risk assessment.
黄曲霉毒素是一种食品污染物,其中一些具有致癌作用。黄曲霉毒素的生物合成途径涉及15个连续步骤。本研究的目的是比较黄曲霉毒素及其前体在三种人类细胞系中的毒性。我们测试了四种黄曲霉毒素及其两种代谢产物;三种早期代谢前体和两种后期生物合成前体。与黄曲霉毒素同时合成的环匹阿尼酸也进行了测试。在三种具有不同生物活化能力的人类细胞系中,用γH2AX试验评估细胞毒性和遗传毒性。我们的结果表明,在这三种细胞系中,遗传毒性最强的化学物质依次为:柄曲霉素(ST)、黄曲霉毒素B1(AFB1)、黄曲霉毒素醇(AFL)、黄曲霉毒素G1(AFG1)和杂色曲霉素(VERA)。黄曲霉毒素M1(AFM1)仅在一种细胞系中表现出遗传毒性。其他测试化合物未表现出任何遗传毒性活性。总体而言,我们的结果表明,所测试化合物的遗传毒性作用机制不同,涉及特定的生物活化途径。此外,黄曲霉毒素的一些代谢前体表现出与AFB1相当或更强的遗传毒性潜力。在制定旨在减少黄曲霉毒素暴露的新策略和进行人类风险评估时,应考虑到这一点。