Deoxycholic acid activates epidermal growth factor receptor and promotes intestinal carcinogenesis by ADAM17-dependent ligand release

J Cell Mol Med. 2018 Sep;22(9):4263-4273. doi: 10.1111/jcmm.13709. Epub 2018 Jun 29.

Abstract

High fat diet is implicated in the elevated deoxycholic acid (DCA) in the intestine and correlated with increased colon cancer risk. However, the potential mechanisms of intestinal carcinogenesis by DCA remain unclarified. Here, we investigated the carcinogenic effects and mechanisms of DCA using the intestinal tumour cells and Apcmin/+ mice model. We found that DCA could activate epidermal growth factor receptor (EGFR) and promote the release of EGFR ligand amphiregulin (AREG), but not HB-EGF or TGF-α in intestinal tumour cells. Moreover, ADAM-17 was required in DCA-induced promotion of shedding of AREG and activation of EGFR/Akt signalling pathway. DCA significantly increased the multiplicity of intestinal tumours and accelerated adenoma-carcinoma sequence in Apcmin/+ mice. ADAM-17/EGFR signalling axis was also activated in intestinal tumours of DCA-treated Apcmin/+ mice, whereas no significant change occurred in tumour adjacent tissues after DCA exposure. Conclusively, DCA activated EGFR and promoted intestinal carcinogenesis by ADAM17-dependent ligand release.

Keywords: a disintegrin and metalloprotease-17; deoxycholic acid; epidermal growth factor receptor; intestinal carcinogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM17 Protein / genetics*
  • ADAM17 Protein / metabolism
  • Adenoma / chemically induced
  • Adenoma / genetics*
  • Adenoma / metabolism
  • Adenoma / pathology
  • Adenomatous Polyposis Coli Protein / deficiency
  • Adenomatous Polyposis Coli Protein / genetics
  • Amphiregulin / genetics*
  • Amphiregulin / metabolism
  • Animals
  • Carcinogenesis / genetics
  • Carcinogenesis / metabolism
  • Carcinogenesis / pathology
  • Cell Line, Tumor
  • Deoxycholic Acid / administration & dosage*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • ErbB Receptors / genetics*
  • ErbB Receptors / metabolism
  • Gene Expression Regulation, Neoplastic*
  • HCT116 Cells
  • Humans
  • Intestinal Neoplasms / chemically induced
  • Intestinal Neoplasms / genetics*
  • Intestinal Neoplasms / metabolism
  • Intestinal Neoplasms / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Protein Binding
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction

Substances

  • Adenomatous Polyposis Coli Protein
  • Amphiregulin
  • Areg protein, mouse
  • adenomatous polyposis coli protein, mouse
  • Deoxycholic Acid
  • EGFR protein, mouse
  • ErbB Receptors
  • Proto-Oncogene Proteins c-akt
  • ADAM17 Protein
  • Adam17 protein, mouse