Dose- and time-dependent effects of phenobarbital on gene expression profiling in human hepatoma HepaRG cells

Toxicol Appl Pharmacol. 2009 Feb 1;234(3):345-60. doi: 10.1016/j.taap.2008.11.008. Epub 2008 Nov 21.

Abstract

Phenobarbital (PB) induces or represses a wide spectrum of genes in rodent liver. Much less is known about its effects in human liver. We used pangenomic cDNA microarrays to analyze concentration- and time-dependent gene expression profile changes induced by PB in the well-differentiated human HepaRG cell line. Changes in gene expression profiles clustered at specific concentration ranges and treatment times. The number of correctly annotated genes significantly modulated by at least three different PB concentration ranges (spanning 0.5 to 3.2 mM) at 20 h exposure amounted to 77 and 128 genes (p< or =0.01) at 2- and 1.8-fold filter changes, respectively. At low concentrations (0.5 and 1 mM), PB-responsive genes included the well-recognized CAR- and PXR-dependent responsive cytochromes P450 (CYP2B6, CYP3A4), sulfotransferase 2A1 and plasma transporters (ABCB1, ABCC2), as well as a number of genes critically involved in various metabolic pathways, including lipid (CYP4A11, CYP4F3), vitamin D (CYP24A1) and bile (CYP7A1 and CYP8B1) metabolism. At concentrations of 3.2 mM or higher after 20 h, and especially 48 h, increased cytotoxic effects were associated with disregulation of numerous genes related to oxidative stress, DNA repair and apoptosis. Primary human hepatocyte cultures were also exposed to 1 and 3.2 mM PB for 20 h and the changes were comparable to those found in HepaRG cells treated under the same conditions. Taken altogether, our data provide further evidence that HepaRG cells closely resemble primary human hepatocytes and provide new information on the effects of PB in human liver. These data also emphasize the importance of investigating dose- and time-dependent effects of chemicals when using toxicogenomic approaches.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Carcinoma, Hepatocellular / enzymology
  • Carcinoma, Hepatocellular / genetics*
  • Cell Line, Tumor
  • Cluster Analysis
  • Cytochrome P-450 Enzyme System / drug effects
  • Cytochrome P-450 Enzyme System / genetics
  • Dose-Response Relationship, Drug
  • Gene Expression Profiling* / methods
  • Gene Expression Regulation, Enzymologic / drug effects*
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Hepatocytes / drug effects*
  • Hepatocytes / enzymology
  • Humans
  • Liver Neoplasms / enzymology
  • Liver Neoplasms / genetics*
  • Oligonucleotide Array Sequence Analysis
  • Phenobarbital / pharmacology*
  • Phenobarbital / toxicity
  • Principal Component Analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors

Substances

  • Adenosine Triphosphate
  • Cytochrome P-450 Enzyme System
  • Phenobarbital