Gauthier Thierry, Duarte-Hospital Carolina, Vignard Julien, Boutet-Robinet Elisa, Sulyok Michael, Snini Selma P, Alassane-Kpembi Imourana, Lippi Yannick, Puel Sylvie, Oswald Isabelle P, Puel Olivier
Toxalim (Research Centre in Food Toxicology), Université de Toulouse, INRA, ENVT, INP-Purpan, UPS, Toulouse, France.
Toxalim (Research Centre in Food Toxicology), Université de Toulouse, INRA, ENVT, INP-Purpan, UPS, Toulouse, France.
Environ Int. 2020 Apr;137:105568. doi: 10.1016/j.envint.2020.105568. Epub 2020 Feb 24.
Aflatoxin B (AFB) is the most potent carcinogen among mycotoxins. Its biosynthesis involves the formation of versicolorin A (VerA), whose chemical structure shares many features with AFB. Our data revealed significant levels of VerA in foodstuff from Central Asia and Africa. Given this emerging food risk, it was of prime interest to compare the toxic effects of the two mycotoxins against cells originating from the intestinal tract. We used human colon cell lines (Caco-2, HCT116) to investigate the cytotoxic process induced by the two mycotoxins. Contrary to AFB, a low dose of VerA (1 µM) disturbed the expression level of thousands of genes (18 002 genes). We show that the cytotoxic effects of low doses of VerA (1-20 µM) were stronger than the same low doses of AFB in both Caco-2 and HCT116 cell lines. In Caco-2 cells, VerA induced DNA strand breaks that led to apoptosis and reduced DNA replication of dividing cells, consequently inhibiting cell proliferation. Although VerA was able to induce the p53 signaling pathway in p53 wild-type HCT116 cells, its toxicity process did not mainly rely on p53 expression since similar cytotoxic effects were also observed in HCT116 cells that do not express p53. In conclusion, this study provides evidence of the risk of food contamination by VerA and shed light on its toxicological effect on human colon cells.
黄曲霉毒素B(AFB)是霉菌毒素中最具致癌性的物质。其生物合成涉及杂色曲霉素A(VerA)的形成,杂色曲霉素A的化学结构与AFB有许多共同特征。我们的数据显示,中亚和非洲的食品中存在大量的VerA。鉴于这种新出现的食品风险,比较这两种霉菌毒素对肠道来源细胞的毒性作用成为首要关注的问题。我们使用人结肠癌细胞系(Caco-2、HCT116)来研究这两种霉菌毒素诱导的细胞毒性过程。与AFB不同,低剂量的VerA(1 μM)会干扰数千个基因(18002个基因)的表达水平。我们发现,在Caco-2和HCT116细胞系中,低剂量的VerA(1-20 μM)的细胞毒性作用比相同低剂量的AFB更强。在Caco-2细胞中,VerA诱导DNA链断裂,导致细胞凋亡,并减少分裂细胞的DNA复制,从而抑制细胞增殖。尽管VerA能够在p53野生型HCT116细胞中诱导p53信号通路,但其毒性过程并不主要依赖于p53的表达,因为在不表达p53的HCT116细胞中也观察到了类似的细胞毒性作用。总之,本研究提供了VerA污染食品的风险证据,并阐明了其对人结肠细胞的毒理学效应。