Clinical Relevance of the Constitutive Androstane Receptor.


Journal

Drug metabolism and disposition: the biological fate of chemicals
ISSN: 1521-009X
Titre abrégé: Drug Metab Dispos
Pays: United States
ID NLM: 9421550

Informations de publication

Date de publication:
07 2022
Historique:
received: 22 03 2021
accepted: 10 02 2022
pubmed: 4 3 2022
medline: 14 7 2022
entrez: 3 3 2022
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 35236665
pii: dmd.121.000483
doi: 10.1124/dmd.121.000483
doi:

Substances chimiques

Constitutive Androstane Receptor 0
Receptors, Cytoplasmic and Nuclear 0
Transcription Factors 0
Xenobiotics 0
Glucose IY9XDZ35W2

Types de publication

Journal Article Review Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1010-1018

Subventions

Organisme : NCI NIH HHS
ID : R01 CA262084
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM121550
Pays : United States
Organisme : NIAAA NIH HHS
ID : R21 AA028521
Pays : United States

Informations de copyright

Copyright © 2022 by The American Society for Pharmacology and Experimental Therapeutics.

Auteurs

Sydney Stern (S)

Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland.

Ritika Kurian (R)

Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland.

Hongbing Wang (H)

Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland hongbing.wang@rx.umaryland.edu.

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Classifications MeSH