Mode of action and human relevance of THF-induced mouse liver tumors.

Toxicol Lett

BASF Corporation, 1609 Biddle Avenue, DZ 40, Wyandotte, MI 48192, USA. Electronic address:

Published: July 2017

AI Article Synopsis

  • Inhalation of tetrahydrofuran (THF) caused liver tumors in female B6C3F mice, suggesting a non-genotoxic mechanism since no tumors were found in male mice or rats of either sex.
  • The study investigated the role of CAR activation in THF-induced tumors using Car/Pxr knock-out mice, revealing that only wild type female mice showed increases in liver enzyme activities and cell proliferation after exposure to THF.
  • The findings point to CAR activation as a likely mediator of THF's carcinogenic effects, with these results having limited relevance to human health.

Article Abstract

In a National Toxicology Program (NTP) bioassay, inhalation of tetrahydrofuran (THF) induced liver tumors in female B6C3F mice but not in male mice or rats of either sex. Since THF is not genotoxic, the NTP concluded this carcinogenic activity was likely mediated via non-genotoxic modes of action (MOA). Based on evidence that THF and phenobarbital share a similar MOA, female Car/Pxr knock-out mice were orally exposed to THF to evaluate the potential role of CAR activation in the MOA for THF-induced liver tumors. Because data from this oral study with Car/Pxr knock-out mice (C57Bl/6) and the inhalation studies with wild type mice (B6C3F) reported by NTP and others were derived from different strains, oral studies with wild type B6C3F and C57Bl/6 mice were conducted to ensure THF responses in both strains were comparable. As seen in inhalation studies with THF, oral exposure of wild type female mice to a maximum tolerated dose of THF increased total P450 content, CAR-related P450 activities, and hepatocyte proliferation; these effects were not observed in Car/Pxr knock-out female mice. This finding supports the hypothesis THF-induced carcinogenicity is likely mediated via CAR activation that has limited, if any, relevance to humans.

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Source
http://dx.doi.org/10.1016/j.toxlet.2017.05.006DOI Listing

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