Phytochemical-induced changes in gene expression of carcinogen-metabolizing enzymes in cultured human primary hepatocytes

K. Gross-Steinmeyer, P. L. Stapleton, F. Liu, J. H. Tracy, T. K. Bammler, S. D. Quigley, F. M. Farin, D. R. Buhler, S. H. Safe, S. C. Strom, D. L. Eaton

Research output: Contribution to journalArticle

54 Scopus citations

Abstract

1. The naturally occurring compounds curcumin (CUR), 3,3′- diindolylmethane (DIM), isoxanthohumol (IXN), 8-prenylnaringenin (8PN), phenethyl isothiocyanate (PEITC) and sulforaphane (SFN) protect animals against chemically induced tumours. Putative chemoprotective mechanisms include modulated expression of hepatic biotransformation enzymes. However, few, if any, studies have used human primary cells as test models. 2. The present study investigated the effects of these phytochemicals on the expression of four carcinogenesis-relevant enzymes - cytochrome P450 (CYP)1A1 and 1A2, NAD(P)H:quinone oxidoreductase (NQO1) and glutathione S-transferase A1 (GSTA1) - in primary cultures of freshly isolated human hepatocytes. 3. Quantitative RT-PCR analyses demonstrated that CYP1A1 was up-regulated by PEITC and DIM in a dose-dependent manner. CYP1A2 transcription was significantly activated following DIM, IXN, 8PN and PEITC treatments. DIM exhibited a remarkably effective induction response of CYP1A1 (474-, 239- and 87-fold at 50, 25 and 10 μM, respectively) and CYP1A2 (113-, 70- and 31-fold at 50, 25 and 10 μM, respectively), that was semiquantitatively reflected in protein levels. NQO1 expression responded to PEITC (11 × at 25 μM), DIM (4.5 × at 50 μM) and SFN (5 × at 10 μM) treatments. No significant effects on GSTA1 transcription were seen. 4. The findings show novel and unexpected effects of these phytochemicals on the expression of human hepatic biotransformation enzymes that play key roles in chemical-induced carcinogenesis.

Original languageEnglish (US)
Pages (from-to)619-632
Number of pages14
JournalXenobiotica
Volume34
Issue number7
DOIs
StatePublished - Jul 2004

ASJC Scopus subject areas

  • Biochemistry
  • Toxicology
  • Pharmacology
  • Health, Toxicology and Mutagenesis

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