Receptor mechanisms mediating differentiation and proliferation effects of retinoids on neuroblastoma cells

Neurosci Lett. 2000 Jan 28;279(2):113-6. doi: 10.1016/s0304-3940(99)00956-8.

Abstract

The aim of this study was to clarify retinoid receptor mechanisms mediating the effects of 9-cis retinoic acid (RA) and investigate the ability of RAR- and RXR-specific analogues to induce differentiation and inhibit proliferation in neuroblastoma cells. Differentiation and the inhibition of proliferation by 9-cis RA, but not all-trans RA, were inhibited by the RXR-homodimer antagonist LG745. The RXR-specific agonist LGD1069 was ineffective at inducing differentiation or inhibiting proliferation, but showed marked synergism with RAR-specific agonists with respect to inhibiting proliferation. These data suggest that the effects of 9-cis RA are mediated via both RXR-homodimers and heterodimers. However, combinations of RAR- and RXR-selective analogues were not as effective at promoting differentiation. This study indicates that different receptor mechanisms are involved in retinoid-induced differentiation and inhibition of proliferation in neuroblastoma cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alitretinoin
  • Bexarotene
  • Cell Differentiation / drug effects*
  • Cell Division / drug effects*
  • Dimerization
  • Humans
  • Neuroblastoma
  • Receptors, Retinoic Acid / physiology*
  • Retinoid X Receptors
  • Retinoids / pharmacology*
  • Tetrahydronaphthalenes / pharmacology
  • Transcription Factors / physiology*
  • Tretinoin / pharmacology
  • Tumor Cells, Cultured

Substances

  • Receptors, Retinoic Acid
  • Retinoid X Receptors
  • Retinoids
  • Tetrahydronaphthalenes
  • Transcription Factors
  • Alitretinoin
  • Tretinoin
  • Bexarotene