Artikel ; Online: Regulation of PXR in drug metabolism: chemical and structural perspectives.
Expert opinion on drug metabolism & toxicology
2024 Band 20, Heft 1-2, Seite(n) 9–23
Abstract: Introduction: Pregnane X receptor (PXR) is a master xenobiotic sensor that transcriptionally controls drug metabolism and disposition pathways. PXR activation by pharmaceutical drugs, natural products, environmental toxins, etc. may decrease drug ... ...
Abstract | Introduction: Pregnane X receptor (PXR) is a master xenobiotic sensor that transcriptionally controls drug metabolism and disposition pathways. PXR activation by pharmaceutical drugs, natural products, environmental toxins, etc. may decrease drug efficacy and increase drug-drug interactions and drug toxicity, indicating a therapeutic value for PXR antagonists. However, PXR's functions in physiological events, such as intestinal inflammation, indicate that PXR activators may be useful in certain disease contexts. Areas covered: We review the reported roles of PXR in various physiological and pathological processes including drug metabolism, cancer, inflammation, energy metabolism, and endobiotic homeostasis. We then highlight specific cellular and chemical routes that modulate PXR activity and discuss the functional consequences. Databases searched and inclusive dates: PubMed, 1 January 1980 to 10 January 2024. Expert opinion: Knowledge of PXR's drug metabolism function has helped drug developers produce small molecules without PXR-mediated metabolic liabilities, and further understanding of PXR's cellular functions may offer drug development opportunities in multiple disease settings. |
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Mesh-Begriff(e) | Humans ; Pregnane X Receptor/metabolism ; Receptors, Steroid/metabolism ; Inactivation, Metabolic ; Inflammation |
Chemische Substanzen | Pregnane X Receptor ; Receptors, Steroid |
Sprache | Englisch |
Erscheinungsdatum | 2024-01-28 |
Erscheinungsland | England |
Dokumenttyp | Journal Article ; Review |
ZDB-ID | 2214462-6 |
ISSN | 1744-7607 ; 1742-5255 |
ISSN (online) | 1744-7607 |
ISSN | 1742-5255 |
DOI | 10.1080/17425255.2024.2309212 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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