Suppression of Cytochrome P450 Cyp1A-1 Induction in Murine Hepatoma 1c1c7-Cells by 12-O-Tetradecanoylphorbol-13-Acetate and Inhibitors of Protein Kinase C

Treatment of murine hepatoma lclc7 cultures with dibenz[a,c]anthracene (DB[a,c]A)-induced P450 Cyp1a-1, as indicated by analyses of CYP1A1 mRNA and 7-ethoxyresorufin O-deethylase (EROD) activity. Pretreatment of cultures with 12-O-tetradecanoylphorbol-13-acetate (TPA) for as short as 1 h reduced protein kinase C (PKC) activity and resulted in a temporary suppression of EROD induction. The dose-response curves defining the TPA-dependent suppression of EROD induction and PKC down-regulation were very similar, as were the initial kinetics of PKC loss and the times of TPA pretreatment required for suppression of EROD induction. The effects of TPA could not be mimicked by 4α-TPA, an analog incapable of activating and down-regulating PKC. Pretreatment of cultures with the protein kinase inhibitors staurosporine, calphostin C, or H7 resulted in dose-dependent suppressions of EROD induction. However, the suppressive and cytotoxic effects of these agents could be separated from one another in the case of only H7. HA 1004, an analog of H7 that inhibits the same spectrum of protein kinases as H7 except for PKC, did not inhibit DBIa,clA induction of EROD. Pretreatment of cultures with H7, but not HA 1004, suppressed the accumulation of CYP1A1 mRNA that normally occurred following treatment with DBIa,cIA. Collectively, these studies suggest that PKC plays a role in the processes involved in the induction of Cyp1a-1.