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Evaluation of the mode of action and human relevance of liver tumors in male mice treated with epyrifenacil.

Authors :
Fukunaga S
Ogata K
Eguchi A
Matsunaga K
Sakurai K
Abe J
Cohen SM
Asano H
Source :
Regulatory toxicology and pharmacology : RTP [Regul Toxicol Pharmacol] 2022 Dec; Vol. 136, pp. 105268. Date of Electronic Publication: 2022 Oct 06.
Publication Year :
2022

Abstract

Epyrifenacil (trademark name: Rapidicil®), a novel protoporphyrinogen oxidase (PPO)-inhibiting herbicide, induces hepatocellular adenomas and carcinomas in male CD-1 mice after 78 weeks treatment. The mode of action (MOA) of these mouse liver tumors and their relevance to humans was assessed based on the 2006 International Programme on Chemical Safety (IPCS) Human Relevance Framework. Epyrifenacil is not genotoxic and induced liver tumors via the postulated porphyria-mediated cytotoxicity MOA with the following key events: (#1) PPO inhibition; (#2) porphyrin accumulation; (#3) hepatocellular injury; with (#4) subsequent regenerative cell proliferation; and ultimately (#5) development of liver tumors. This article evaluates the weight of evidence for this MOA based on the modified Bradford Hill criteria. The MOA data were aligned with the dose and temporal concordance, biological plausibility, coherence, strength, consistency, and specificity for a porphyria-mediated cytotoxicity MOA while excluding other alternative MOAs. Although the postulated MOA could qualitatively potentially occur in humans, we demonstrate that it is unlikely to occur in humans because of quantitative toxicodynamic and toxicokinetic differences between mice and humans. Therefore, this MOA is considered not relevant to humans, utilizing the IPCS Human Relevance Framework; consequently, a nonlinear, threshold dose response would be appropriate for human risk assessment.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: All authors reports financial support was provided by Sumitomo Chemical Co Ltd. Satoki Fukunaga reports a relationship with Sumitomo Chemical Co Ltd that includes: employment. Keiko Ogata, Ayumi Eguchi, Kohei Matsunaga, Kengo Sakurai, Jun Abe and Hiroyuki Asano reports a relationship with Sumitomo Chemical Co Ltd that includes: employment. Samuel M Cohen reports a relationship with Sumitomo Chemical Co Ltd that includes: consulting or advisory.<br /> (Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1096-0295
Volume :
136
Database :
MEDLINE
Journal :
Regulatory toxicology and pharmacology : RTP
Publication Type :
Academic Journal
Accession number :
36210011
Full Text :
https://doi.org/10.1016/j.yrtph.2022.105268