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Retinoid X Receptor agonists as selective modulators of the immune system for the treatment of cancer.

Abstract
Upon heterodimerizing with other nuclear receptors, retinoid X receptors (RXR) act as ligand-dependent transcription factors, regulating transcription of critical signaling pathways that impact numerous hallmarks of cancer. By controlling both inflammation and immune responses, ligands that activate RXR can modulate the tumor microenvironment. Several small molecule agonists of these essential receptors have been synthesized. Historically, RXR agonists were tested for inhibition of growth in cancer cells, but more recent drug discovery programs screen new molecules for inhibition of inflammation or activation of immune cells. Bexarotene is the first successful example of an effective therapeutic that molecularly targets RXR; this drug was approved to treat cutaneous T cell lymphoma and is still used as a standard of care treatment for this disease. No additional RXR agonists have yet achieved FDA approval, but several promising novel compounds are being developed. In this review, we provide an overview of the multiple mechanisms by which RXR signaling regulates inflammation and tumor immunity. We also discuss the potential of RXR-dependent immune cell modulation for the treatment or prevention of cancer and concomitant challenges and opportunities.
AuthorsAna S Leal, Pei-Yu Hung, Afrin Sultana Chowdhury, Karen T Liby
JournalPharmacology & therapeutics (Pharmacol Ther) Vol. 252 Pg. 108561 (Dec 2023) ISSN: 1879-016X [Electronic] England
PMID37952906 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2023 Elsevier Inc. All rights reserved.
Chemical References
  • Retinoid X Receptors
  • Bexarotene
Topics
  • Humans
  • Retinoid X Receptors (agonists, metabolism)
  • Bexarotene (pharmacology, therapeutic use)
  • Neoplasms (drug therapy)
  • Inflammation
  • Immune System (metabolism)
  • Tumor Microenvironment

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