The present study has determined the effects of 6-nitrochrysene (6-NC) on h
uman cytochrome P450-dependent monooxygenases in human hepatoma HepG2 cells
. Treatment of HepG2 cells with 6-NC increased the activities of microsomal
benzo[a]pyrene hydroxylase, 7-ethoxycoumarin and 7-ethoxyresorufin O-deeth
ylases, cytosolic glutathione S-transferase and N-acetyltransferase, and S9
metabolic activation of 6-NC in the Ames mutagenicity test. Immunoblot and
RNA blot analyses revealed that 6-NC induced CYP1A1 protein and mRNA level
s in the hepatoma cells. Nuclear transcription assay demonstrated that 6-NC
increased the transcription rate of CYP1A1 gene in HepG2 cells. Treatment
of human lung carcinoma NCI-H322 cells with 6-NC increased benzo[a]pyrene h
ydroxylase activity and CYP1A1 protein and mRNA levels. These results demon
strate that 6-NC is an inducer of human CYP1A1 and the induction occurs at
a transcriptional level in HepG2 cells. The ability of 6-NC to induce liver
and lung CYP1A1 may be an important factor to consider in assessing 6-NC m
etabolism and toxicity in humans. (C) 2000 Elsevier Science Ireland Ltd. Al
l rights reserved.