Characterization of liver injury, oval cell proliferation and cholangiocarcinogenesis in glutathione S-transferase A3 knockout mice

• Published in: Carcinogenesis (New York) 2017-07, Vol.38 (7), p.717-727
• Main Authors: Crawford, Dana R, Ilic, Zoran, Guest, Ian, Milne, Ginger L, Hayes, John D, Sell, Stewart
• Format: Article
• Language: English
• Subjects: Aflatoxin B1 - administration & dosage; Animals; Carcinogenesis - genetics; Cell Proliferation - drug effects; Cholangiocarcinoma - genetics; Cholangiocarcinoma - physiopathology; Cytochrome P-450 CYP1A2 - genetics; Cytochrome P-450 CYP3A - genetics; DNA Adducts - drug effects; F2-Isoprostanes - administration & dosage; Female; Glutathione Transferase - biosynthesis; Glutathione Transferase - genetics; Humans; Male; Membrane Proteins - genetics; Mice; Mice, Knockout; Original Manuscript; Oxidative Stress - drug effects; Sex Characteristics
• ISSN: 0143-3334; 1460-2180
• DOI: 10.1093/carcin/bgx048

We recently generated glutathione S-transferase (GST) A3 knockout (KO) mice as a novel model to study the risk factors for liver cancer. GSTA3 KO mice are sensitive to the acute cytotoxic and genotoxic effects of aflatoxin B1 (AFB1), confirming the crucial role of GSTA3 in resistance to AFB1. We now report histopathological changes, tumor formation, biochemical changes and gender response following AFB1 treatment as well as the contribution of oxidative stress. Using a protocol of weekly 0.5 mg AFB1/kg administration, we observed extensive oval (liver stem) cell (OC) proliferation within 1-3 weeks followed by microvesicular lipidosis, megahepatocytes, nuclear inclusions, cholangiomas and small nodules. Male and female GSTA3 KO mice treated with 12 and 24 weekly AFB1 injections followed by a rest period of 12 and 6 months, respectively, all had grossly distorted livers with macro- and microscopic cysts, hepatocellular nodules, cholangiomas and cholangiocarcinomas and OC proliferation. We postulate that the prolonged AFB1 treatment leads to inhibition of hepatocyte proliferation, which is compensated by OC proliferation and eventually formation of cholangiocarcinoma (CCA). At low-dose AFB1, male KO mice showed less extensive acute liver injury, OC proliferation and AFB1-DNA adducts than female KO mice. There were no significant compensatory changes in KO mice GST subunits, GST enzymatic activity, epoxide hydrolase, or CYP1A2 and CYP3A11 levels. Finally, there was a modest increase in F2-isoprostane and isofuran in KO mice that confirmed putative GSTA3 hydroperoxidase activity in vivo for the first time.