Invasion of normal human fibroblasts induced by v-Fos is independent of proliferation, immortalization, and the tumor suppressors p16INK4a and p53

Mol Cell Biol. 2004 Feb;24(4):1540-59. doi: 10.1128/MCB.24.4.1540-1559.2004.

Abstract

Invasion is generally perceived to be a late event during the progression of human cancer, but to date there are no consistent reports of alterations specifically associated with malignant conversion. We provide evidence that the v-Fos oncogene induces changes in gene expression that render noninvasive normal human diploid fibroblasts highly invasive, without inducing changes in growth factor requirements or anchorage dependence for proliferation. Furthermore, v-Fos-stimulated invasion is independent of the pRb/p16(INK4a) and p53 tumor suppressor pathways and telomerase. We have performed microarray analysis using Affymetrix GeneChips, and the gene expression profile of v-Fos transformed cells supports its role in the regulation of invasion, independent from proliferation. We also demonstrate that invasion, but not proliferation, is dependent on the activity of the up-regulated epidermal growth factor receptor. Taken together, these results indicate that AP-1-directed invasion could precede deregulated proliferation during tumorigenesis and that sustained activation of AP-1 could be the epigenetic event required for conversion of a benign tumor into a malignant one, thereby explaining why many malignant human tumors present without an obvious premalignant hyperproliferative dysplastic lesion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / pathology*
  • Cyclin-Dependent Kinase Inhibitor p16 / metabolism*
  • DNA Damage
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Fibroblasts / metabolism*
  • Fibroblasts / pathology*
  • Gene Expression Profiling
  • Humans
  • Karyotyping
  • Mice
  • Neoplasm Invasiveness / genetics
  • Neoplasm Invasiveness / pathology*
  • Oncogene Proteins v-fos / genetics
  • Oncogene Proteins v-fos / metabolism*
  • Signal Transduction
  • Telomerase / genetics
  • Telomerase / metabolism
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*
  • Up-Regulation
  • Wound Healing

Substances

  • Cyclin-Dependent Kinase Inhibitor p16
  • Oncogene Proteins v-fos
  • Tumor Suppressor Protein p53
  • ErbB Receptors
  • Telomerase