Jagged1-mediated Notch activation induces epithelial-to-mesenchymal transition through Slug-induced repression of E-cadherin

J Exp Med. 2007 Nov 26;204(12):2935-48. doi: 10.1084/jem.20071082. Epub 2007 Nov 5.

Abstract

Aberrant expression of Jagged1 and Notch1 are associated with poor outcome in breast cancer. However, the reason that Jagged1 and/or Notch overexpression portends a poor prognosis is unknown. We identify Slug, a transcriptional repressor, as a novel Notch target and show that elevated levels of Slug correlate with increased expression of Jagged1 in various human cancers. Slug was essential for Notch-mediated repression of E-cadherin, which resulted in beta-catenin activation and resistance to anoikis. Inhibition of ligand-induced Notch signaling in xenografted Slug-positive/E-cadherin-negative breast tumors promoted apoptosis and inhibited tumor growth and metastasis. This response was associated with down-regulated Slug expression, reexpression of E-cadherin, and suppression of active beta-catenin. Our findings suggest that ligand-induced Notch activation, through the induction of Slug, promotes tumor growth and metastasis characterized by epithelial-to-mesenchymal transition and inhibition of anoikis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Binding Sites
  • Breast / cytology
  • Breast Neoplasms / genetics
  • Cadherins / antagonists & inhibitors*
  • Cadherins / genetics
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / physiology*
  • Cell Line
  • Epithelial Cells / physiology*
  • Female
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / physiology*
  • Jagged-1 Protein
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology*
  • Mesoderm / cytology
  • Mesoderm / physiology*
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / physiology*
  • Serrate-Jagged Proteins
  • Snail Family Transcription Factors
  • Transcription Factors / genetics
  • Transcription Factors / physiology*

Substances

  • Cadherins
  • Calcium-Binding Proteins
  • Intercellular Signaling Peptides and Proteins
  • JAG1 protein, human
  • Jagged-1 Protein
  • Membrane Proteins
  • NOTCH1 protein, human
  • Receptor, Notch1
  • SNAI1 protein, human
  • Serrate-Jagged Proteins
  • Snail Family Transcription Factors
  • Transcription Factors