Butyrate-induced differentiation of Caco-2 cells is mediated by vitamin D receptor

Biochem Biophys Res Commun. 2001 Nov 2;288(3):690-6. doi: 10.1006/bbrc.2001.5832.

Abstract

Butyrate in combination with 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] produces a synergistic effect on cell differentiation of human colon cancer cells (Caco-2). The objective of this study was to confirm the role of the vitamin D receptor (VDR) in butyrate-induced cell differentiation of Caco-2. We studied the effects of the novel VDR antagonist ZK 191732 on butyrate-induced cell differentiation and on p21Waf1/Cip1 expression. Butyrate induced cell differentiation which was further enhanced after addition of 1,25-(OH)2D3. Experiments using ZK 191732 indicate that the synergistic effect of butyrate and 1,25-(OH)2D3 was due to butyrate-induced upregulation of VDR. While butyrate alone increased expression of p21Waf1/Cip1 and combined exposure of butyrate and 1,25-(OH)2D3 resulted in a synergistic amplification, p21Waf1/Cip1 expression did not change from the control level after treatment with butyrate plus ZK 191732. These data further imply that butyrate-induced differentiation and p21Waf1/Cip1 expression of Caco-2 cells occur via upregulation of VDR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Butyrates / pharmacology*
  • Caco-2 Cells
  • Cell Differentiation / drug effects*
  • Cell Differentiation / physiology
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins / metabolism
  • Drug Interactions
  • Gene Expression / drug effects
  • Humans
  • Receptors, Calcitriol / biosynthesis
  • Receptors, Calcitriol / drug effects
  • Receptors, Calcitriol / physiology*
  • Thiazoles / pharmacology*
  • Up-Regulation / drug effects

Substances

  • Butyrates
  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Receptors, Calcitriol
  • Thiazoles
  • ZK 191732