Breast cancer cells induce stromal fibroblasts to express MMP-9 via secretion of TNF-alpha and TGF-beta

J Cell Sci. 2005 May 15;118(Pt 10):2143-53. doi: 10.1242/jcs.02334. Epub 2005 Apr 26.

Abstract

We used 2D-cocultures employing fibroblasts of different genetic backgrounds and MCF10A-derived human breast epithelial cells of increasingly malignant potential to investigate tumor-stroma interactions in breast cancer and to identify possible signaling pathways involved. Tumor cells induced expression of matrix-metalloproteinase 9 (MMP-9) in fibroblasts in a pattern dependent on the degree of their malignancy. In-situ zymography localized the main gelatinolytic activity around stromal cells in cocultures and xenografted tumors. Use of Smad3 knockout fibroblasts, small molecule inhibitors, and neutralizing antibodies showed that MMP-9 expression was induced by tumor cell-derived TNF-alpha and TGF-beta, dependent on Smad-, Ras-, and PI3-kinase-signaling, and likewise modulated by subsequent HGF- and EGF-signaling. Together, our results indicate that MMP-9 levels in tumor fibroblasts are regulated by a complex tumor-stroma cross-talk, involving multiple ligands and cellular signaling pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Coculture Techniques
  • Epidermal Growth Factor / physiology
  • Epithelial Cells / metabolism
  • Fibroblasts / metabolism*
  • Humans
  • Matrix Metalloproteinase 9 / metabolism*
  • Mice
  • Mice, Knockout
  • Mitogen-Activated Protein Kinases / physiology
  • Neoplasm Transplantation
  • Phosphatidylinositol 3-Kinases / physiology
  • Protein Kinases / metabolism
  • Signal Transduction / physiology
  • Smad3 Protein / genetics
  • Stromal Cells / metabolism
  • Transforming Growth Factor beta / metabolism*
  • Transplantation, Heterologous
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Smad3 Protein
  • Smad3 protein, mouse
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Epidermal Growth Factor
  • Protein Kinases
  • Phosphatidylinositol 3-Kinases
  • Mitogen-Activated Protein Kinases
  • Matrix Metalloproteinase 9