The flavonoid apigenin suppresses vitamin D receptor expression and vitamin D responsiveness in normal human keratinocytes

Biochem Biophys Res Commun. 2000 Feb 5;268(1):237-41. doi: 10.1006/bbrc.2000.2099.

Abstract

Apigenin, a flavonoid with chemopreventive properties, induces cellular growth arrest, with concomitant inhibition of intracellular signaling cascades and decreased proto-oncogene expression. We report that apigenin potently inhibited vitamin D receptor (VDR) mRNA and protein expression in human keratinocytes without changes in VDR mRNA half-life. Concurrently, downregulation of retinoid X receptor alpha, a dramatic loss of c-myc mRNA, and upregulation of p21(WAF1) took place. Furthermore, a nearly complete suppression of vitamin D responsiveness was observed as estimated by induction of 24-hydroxylase mRNA. The apigenin effect on VDR expression was shared by some other (quercetine and fisetine) but not all tested flavonoids. Interestingly, the apigenin-mediated VDR suppression was counteracted by the NFkappaB inhibitors sodium salicylate and caffeic acid phenethyl ester. The presented results propose suppression of nuclear receptor levels as a novel mechanism whereby flavonoids exert their pleiotropic effects. This study may also contribute to the understanding of the regulation of VDR expression in epidermal keratinocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apigenin
  • Cells, Cultured
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / genetics
  • Flavonoids / pharmacology*
  • Gene Expression / drug effects
  • Half-Life
  • Humans
  • Keratinocytes / drug effects*
  • Keratinocytes / metabolism*
  • NF-kappa B / metabolism
  • Proto-Oncogene Mas
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Calcitriol / genetics*
  • Receptors, Calcitriol / metabolism*
  • Receptors, Retinoic Acid / genetics
  • Retinoid X Receptors
  • Signal Transduction / drug effects
  • Transcription Factors / genetics
  • Vitamin D / pharmacology*

Substances

  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Flavonoids
  • MAS1 protein, human
  • NF-kappa B
  • Proto-Oncogene Mas
  • RNA, Messenger
  • Receptors, Calcitriol
  • Receptors, Retinoic Acid
  • Retinoid X Receptors
  • Transcription Factors
  • Vitamin D
  • Apigenin