Stromal fibroblasts activated by tumor cells promote angiogenesis in mouse gastric cancer

J Biol Chem. 2008 Jul 11;283(28):19864-71. doi: 10.1074/jbc.M800798200. Epub 2008 May 21.

Abstract

Myofibroblasts, also known as activated fibroblasts, constitute an important niche for tumor development through the promotion of angiogenesis. However, the mechanism of stromal fibroblast activation in tumor tissues has not been fully understood. A gastric cancer mouse model (Gan mice) was recently constructed by simultaneous activation of prostaglandin (PG) E2 and Wnt signaling in the gastric mucosa. Because both the PGE2 and Wnt pathways play a role in human gastric tumorigenesis, the Gan mouse model therefore recapitulates the molecular etiology of human gastric cancer. Microvessel density increased significantly in Gan mouse tumors. Moreover, the expression of vascular endothelial growth factor A (VEGFA) was predominantly induced in the stromal cells of gastric tumors. Immunohistochemistry suggested that VEGFA-expressing cells in the stroma were alpha-smooth muscle actin-positive myofibroblasts. Bone marrow transplantation experiments indicated that a subset of gastric myofibroblasts is derived from bone marrow. Importantly, the alpha-smooth muscle actin index in cultured fibroblasts increased significantly when stimulated with the conditioned medium of Gan mouse tumor cells, indicating that gastric tumor cells activate stromal fibroblasts. Furthermore, conditioned medium of Gan mouse tumor cells induced VEGFA expression both in embryonic and gastric fibroblasts, which further accelerated the tube formation of human umbilical vein endothelial cells in vitro. Notably, stimulation of fibroblasts with PGE2 and/or Wnt1 did not induce VEGFA expression, thus suggesting that factors secondarily induced by PGE2 and Wnt signaling in the tumor cells are responsible for activation of stromal fibroblasts. Such tumor cell-derived factors may therefore be an effective target for chemoprevention against gastric cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Animals
  • Dinoprostone / metabolism
  • Dinoprostone / pharmacology
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Fibroblasts / metabolism*
  • Fibroblasts / pathology
  • Gastric Mucosa / metabolism*
  • Gastric Mucosa / pathology
  • Gene Expression Regulation, Neoplastic* / drug effects
  • Gene Expression Regulation, Neoplastic* / genetics
  • Humans
  • Mice
  • Mice, Transgenic
  • Muscle, Smooth / metabolism
  • Muscle, Smooth / pathology
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Neoplasms, Experimental / genetics
  • Neoplasms, Experimental / metabolism
  • Neoplasms, Experimental / pathology
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / metabolism*
  • Neovascularization, Pathologic / pathology
  • Oxytocics / metabolism
  • Oxytocics / pharmacology
  • Stomach Neoplasms / genetics
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / pathology
  • Stromal Cells / metabolism
  • Stromal Cells / pathology
  • Tumor Cells, Cultured
  • Vascular Endothelial Growth Factor A / biosynthesis*
  • Vascular Endothelial Growth Factor A / genetics
  • Wnt1 Protein / genetics
  • Wnt1 Protein / metabolism
  • Wnt1 Protein / pharmacology

Substances

  • Actins
  • Neoplasm Proteins
  • Oxytocics
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • WNT1 protein, human
  • Wnt1 Protein
  • Wnt1 protein, mouse
  • vascular endothelial growth factor A, mouse
  • Dinoprostone