Ochratoxin A and Mitotic Disruption: Mode of Action Analysis of Renal Tumor Formation by Ochratoxin A

被引:79
作者
Mally, Angela [1 ]
机构
[1] Univ Wurzburg, Dept Toxicol, D-97078 Wurzburg, Germany
关键词
ochratoxin A; carcinogenesis; mitosis; MoA; OXIDATIVE DNA-DAMAGE; HUMAN PROXIMAL TUBULE; MYCOTOXIN OCHRATOXIN; IN-VITRO; SALMONELLA-TYPHIMURIUM; MESSENGER-RNA; HISTONE ACETYLTRANSFERASES; NEPHROTOXIN OCHRATOXIN; GENDER DIFFERENCE; URINARY-BLADDER;
D O I
10.1093/toxsci/kfs105
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The mycotoxin and food contaminant ochratoxin A (OTA) is a potent renal carcinogen in rodents, but its mode of action (MoA) is still poorly defined. In 2006, the European Food Safety Authority concluded that there is a "lack of evidence for the existence of OTA-DNA adducts" and thus insufficient evidence to establish DNA reactivity as a MoA for tumor formation by OTA. In reviewing the available database on OTA toxicity, a MoA for renal carcinogenicity of OTA is developed that involves a combination of genetic instability and increased proliferative drive as consequences of OTA-mediated disruption of mitosis, whereby the organ- and site-specificity of tumor formation by OTA is determined by selective renal uptake of OTA into the proximal tubule epithelium. The proposed MoA is critically assessed with respect to concordance of dose-response of the suggested key events and tumor formation, their temporal association, consistency, and biological plausibility. Uncertainties, data gaps and needs for further research are highlighted.
引用
收藏
页码:315 / 330
页数:16
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