Clinical Relevance of the Constitutive Androstane Receptor

Drug Metab Dispos. 2022 Jul;50(7):1010-1018. doi: 10.1124/dmd.121.000483. Epub 2022 Mar 2.

Abstract

Constitutive androstane receptor (CAR) (NR1I3), a xenobiotic receptor, has long been considered a master mediator of drug disposition and detoxification. Accumulating evidence indicates that CAR also participates in various physiologic and pathophysiological pathways regulating the homeostasis of glucose, lipid, and bile acids, and contributing to cell proliferation, tissue regeneration and repair, as well as cancer development. The expression and activity of CAR can be regulated by various factors, including small molecular modulators, CAR interaction with other transcription factors, and naturally occurring genetic variants. Given that the influence of CAR has extended beyond the realm of drug metabolism and disposition and has expanded into a potential modulator of human diseases, growing efforts have centered on understanding its clinical relevance and impact on human pathophysiology. This review highlights the current information available regarding the contribution of CAR to various metabolic disorders and cancers and ponders the possible challenges that might arise from pursuing CAR as a potential therapeutic target for these diseases. SIGNIFICANCE STATEMENT: The growing importance of the constitutive androstane receptor (CAR) in glucose and lipid metabolism as well as its potential implication in cell proliferation emphasizes a need to keenly understand the biological function and clinical impact of CAR. This minireview captures the clinical relevance of CAR by highlighting its role in metabolic disorders and cancer development.

Publication types

  • Review
  • Research Support, N.I.H., Extramural

MeSH terms

  • Constitutive Androstane Receptor*
  • Glucose
  • Humans
  • Receptors, Cytoplasmic and Nuclear*
  • Transcription Factors
  • Xenobiotics / metabolism

Substances

  • Constitutive Androstane Receptor
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Xenobiotics
  • Glucose