Regulation of CAR and PXR Expression in Health and Disease

Cells. 2020 Oct 31;9(11):2395. doi: 10.3390/cells9112395.

Abstract

Pregnane X receptor (PXR, NR1I2) and constitutive androstane receptor (CAR, NR1I3) are members of the nuclear receptor superfamily that mainly act as ligand-activated transcription factors. Their functions have long been associated with the regulation of drug metabolism and disposition, and it is now well established that they are implicated in physiological and pathological conditions. Considerable efforts have been made to understand the regulation of their activity by their cognate ligand; however, additional regulatory mechanisms, among which the regulation of their expression, modulate their pleiotropic effects. This review summarizes the current knowledge on CAR and PXR expression during development and adult life; tissue distribution; spatial, temporal, and metabolic regulations; as well as in pathological situations, including chronic diseases and cancers. The expression of CAR and PXR is modulated by complex regulatory mechanisms that involve the interplay of transcription factors and also post-transcriptional and epigenetic modifications. Moreover, many environmental stimuli affect CAR and PXR expression through mechanisms that have not been elucidated.

Keywords: CAR; PXR; expression; regulation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alternative Splicing
  • Animals
  • Biological Clocks
  • Constitutive Androstane Receptor
  • Energy Metabolism
  • Epigenesis, Genetic*
  • Gene Expression Regulation, Developmental*
  • Hepatocytes / physiology
  • Humans
  • Inactivation, Metabolic
  • Mice
  • Pregnane X Receptor / physiology*
  • Protein Isoforms
  • Receptors, Cytoplasmic and Nuclear / physiology*
  • Tissue Distribution
  • Transcription Factors

Substances

  • Constitutive Androstane Receptor
  • NR1I2 protein, human
  • NR1I3 protein, human
  • Nr1i3 protein, mouse
  • Pregnane X Receptor
  • Protein Isoforms
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors