The liver histology in this group was consistent with multiple nodules of

regeneration (small nodules in 100% of animals) and preneoplastic foci (Figure 1). Distorted lobular architecture was also observed, with increased mitotic index and hepatocellular damage such fibrosis and cirrhosis. The cytologic criteria included nuclear and cytoplasmic changes, multinucleation, centrally located nuclei, prominent nucleoli and increased cell density [22]. The percentage of fibrosis in the liver tissue was determined by morphometric measurement of picrosirius red-stained samples. Data obtained indicate that the extent of fibrotic tissue increased slightly in rats with precancerous lesions and augmented markedly in animals with advanced HCC (control: 1.7 ± 0.1; precancerous lesions: 3.8 ± 1.5; advanced HCC: 12.3 ± 2.9; Y-27632 in vitro p < .05). Determination of lipid peroxidation in liver tissue was performed by the TBARS method, which showed a significant increase of malondialdehyde formation in both groups of DEN-treated rats. TBARS increased by 81% in the PL group when compared to control animals, while rats with advanced HCC had values approximately 25% lower than that of PL group. Liver activity of the antioxidant enzyme SOD was significantly increased in PL rats (+13%) and reduced in the advanced HCC group (-32%) when compared to control animals Selleck Dabrafenib (Table

1). To evaluate the effects of early and advanced HCC on development of fibrosis, the expression of TGF-1β was quantified by measurement of protein expression. Both PL and advanced HCC animals exhibited a significant induction of TGF-1β, which reached a higher extent in the first group (+98%) (Figure 2). Concerning markers of inflammation, eNOS expression was reduced (-60%), whereas iNOS expression increased strongly in animals with advanced HCC (Figure 2). Protein markers related to oxidative stress were also evaluated. The advanced HCC group exhibited a significant induction of NQO1 protein as compared with the control group

(+82%). Rats in the PL group overexpressed nuclear factor Nrf2 (+260%), while in the advanced HCC group Nrf-2 expression was reduced (-56%) and Keap-1 was markedly overexpressed (+308%). Expression of the main isoforms ever of the HSP family (constitutive HSP 73 and stress-inducible HSP72) decreased significantly in animals with advanced HCC (-32% and -74%, respectively) (Figure 3). This study provides evidence of the activation/inhibition of different proteins involved in oxidative stress and cell damage in a multistage animal model of hepatic carcinogenesis. Blood chemistry, liver histology, markers of oxidative stress and expression of different proteins related to HCC pathogenic mechanisms were measured in rats with early/precancerous lesions (PL) or late-stage HCC reached through different protocols of DEN administration. DEN is a potent hepatocarcinogenic agent [23], which is hydrolyzed to nitrosamine, generating an electrophilic radical.