AI Article Synopsis

  • GST-P foci serve as markers for early liver lesions in rat studies on liver cancer development, with furan and diethylnitrosamine (DEN) inducing them differently.
  • Furan exposure leads to a decrease in the number and size of GST-P foci after treatment, unlike DEN, which sees an increase.
  • Gene expression analysis reveals that furan-induced GST-P foci, particularly large ones, exhibit different molecular characteristics, including higher levels of SOX9, setting them apart from DEN-induced foci.

Article Abstract

Glutathione -transferase placental form-positive (GST-P) foci are markers of preneoplastic lesions in rat hepatocarcinogenesis. Our previous studies using reporter gene transgenic rats showed that furan, a hepatocarcinogen in rodents, rapidly induces the formation of GST-P foci after short exposure without reporter gene mutation. We hypothesized that GST-P foci induced by furan may have biological characteristics different from those induced by diethylnitrosamine (DEN), a genotoxic hepatocarcinogen. Accordingly, we compared the cell kinetics of GST-P foci after cessation of DEN treatment and performed comprehensive gene expression in DEN- or furan-induced GST-P foci. The number and area of DEN-induced GST-P foci were increased after cessation of treatment, whereas furan decreased these parameters. Size distribution analysis showed that large furan-induced GST-P foci disappeared after cessation of treatment. Hierarchical cluster analysis showed that all samples from GST-P foci induced by furan were separated from those induced by DEN. SOX9 expression was upregulated in furan-induced GST-P foci and was detected by immunohistochemistry in large furan-induced GST-P foci. Our results indicated that large furan-induced GST-P foci were quite different from DEN-induced GST-P foci at the molecular and cellular levels. And one of the properties of disappearing large GST-P foci were characterized by inclusion of hepatocytes expressing SOX9.

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http://dx.doi.org/10.1177/0192623320948782DOI Listing

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