Mitogen-activated Protein Kinase Inhibits 1,25-dihydroxyvitamin D3-dependent Signal Transduction by Phosphorylating Human Retinoid X Receptor Alpha

J Clin Invest. 1999 Jun;103(12):1729-35. doi: 10.1172/JCI6871.

Abstract

Human retinoid X receptor alpha (hRXR alpha) is a member of the nuclear receptor family of transcriptional regulators. It regulates transcription through its association with several heterodimeric partners, including the vitamin D3 receptor (VDR). Signaling through the VDR is essential for normal calcium homeostasis and has been shown to inhibit the proliferation of cancer cells derived from a number of tissues. Here we show that phosphorylation of hRXR alpha in ras-transformed human keratinocytes through the activated Ras-Raf-mitogen-activated protein kinase (Ras-Raf-MAP kinase) pathway results in attenuated transactivation by the VDR and resistance to the growth inhibitory action of 1,25 dihydroxyvitamin D3 [1,25(OH)2D3] and RXR-specific agonist LG1069 (4-[1-(5,6,7, 8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl) ethenyl]-benzoic acid). Phosphorylation of hRXR alpha occurs at serine 260, a consensus MAP kinase site. Inhibition of MAP kinase activity or point mutagenesis of serine 260 of hRXR alpha reverses the observed resistance to 1,25(OH)2D3 and LG1069. Thus, hRXR alpha is a downstream target of MAP kinase, and its phosphorylation may play an important role in malignant transformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology
  • Bexarotene
  • COS Cells
  • Calcitriol / antagonists & inhibitors*
  • Calcitriol / metabolism
  • Calcitriol / pharmacology
  • Calcium-Calmodulin-Dependent Protein Kinases / antagonists & inhibitors
  • Calcium-Calmodulin-Dependent Protein Kinases / physiology*
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic / drug effects
  • Cell Transformation, Neoplastic / metabolism
  • Drug Resistance, Neoplasm
  • Genes, ras / physiology
  • Humans
  • Keratinocytes / drug effects
  • Keratinocytes / enzymology
  • Keratinocytes / metabolism
  • Mutagenesis, Site-Directed
  • Phenotype
  • Phosphorylation / drug effects
  • Receptors, Calcitriol / metabolism
  • Receptors, Retinoic Acid / metabolism*
  • Retinoid X Receptors
  • Serine / genetics
  • Serine / metabolism
  • Signal Transduction* / drug effects
  • Tetrahydronaphthalenes / pharmacology
  • Transcription Factors / metabolism*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Anticarcinogenic Agents
  • Receptors, Calcitriol
  • Receptors, Retinoic Acid
  • Retinoid X Receptors
  • Tetrahydronaphthalenes
  • Transcription Factors
  • Serine
  • Bexarotene
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Calcitriol