Ursodeoxycholic acid suppresses Cox-2 expression in colon cancer: roles of Ras, p38, and CCAAT/enhancer-binding protein

Nutr Cancer. 2008;60(3):389-400. doi: 10.1080/01635580701883003.

Abstract

In the azoxymethane (AOM) model of experimental rodent colon cancer, cholic acid and its colonic metabolite deoxycholic acid (DCA) strongly promote tumorigenesis. In contrast, we showed that ursodeoxycholic acid (UDCA), a low abundance bile acid, inhibited AOM tumorigenesis. Dietary UDCA also blocked the development of tumors with activated Ras and suppressed cyclooxygenase-2 (Cox-2) upregulation in AOM tumors. In this study, we compared the effect of dietary supplementation with tumor-promoting cholic acid to chemopreventive UDCA on Cox-2 expression in AOM tumors. Cholic acid enhanced Cox-2 upregulation in AOM tumors, whereas UDCA inhibited this increase and concomitantly decreased CCAAT/enhancer binding protein beta (C/EBPbeta), a transcriptional regulator of Cox-2. In HCA-7 colon cancer cells, DCA activated Ras and increased C/EBPbeta and Cox-2 by a mechanism requiring the mitogen-activated protein kinase p38. UDCA inhibited DCA-induced p38 activation and decreased C/EBPbeta and Cox-2 upregulation. Using transient transfections, UDCA inhibited Cox-2 promoter and C/EBP reporter activation by DCA. Transfection with dominant-negative (17)N-Ras abolished DCA-induced p38 activation and C/EBPbeta and Cox-2 upregulation. Taken together, these studies have identified a transcriptional pathway regulating Cox-2 expression involving Ras, p38, and C/EBPbeta that is inhibited by UDCA. These signal transducers are novel targets of UDCA's chemopreventive actions.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Azoxymethane / toxicity
  • CCAAT-Enhancer-Binding Protein-beta / metabolism*
  • Cells, Cultured
  • Chemoprevention
  • Cholic Acid / toxicity
  • Colonic Neoplasms / chemically induced
  • Colonic Neoplasms / enzymology*
  • Cyclooxygenase 2 / drug effects
  • Cyclooxygenase 2 / metabolism*
  • Cyclooxygenase 2 Inhibitors / pharmacology
  • Dietary Supplements
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Genes, ras* / drug effects
  • Genes, ras* / physiology
  • Signal Transduction
  • Transcription Factors / metabolism
  • Transfection
  • Ursodeoxycholic Acid / pharmacology*
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • Cyclooxygenase 2 Inhibitors
  • Transcription Factors
  • Ursodeoxycholic Acid
  • Cyclooxygenase 2
  • p38 Mitogen-Activated Protein Kinases
  • Cholic Acid
  • Azoxymethane