Elevated stromelysin-1 and reduced collagenase-IV expression in invasive rat embryo fibroblasts expressing E1A deletion mutants + T24-H-ras

Int J Cancer. 1992 Jul 9;51(5):761-6. doi: 10.1002/ijc.2910510516.

Abstract

We have studied the in vitro invasive properties of 3 cell lines derived from the co-transfection of rat embryo fibroblasts (REF) with EIA genes deficient in exon 2 and T24-ras. All 3 cell lines showed invasive properties at passage 10 after isolation. Invasive cells expressed elevated levels of stromelysin-1 and reduced levels of 68-kDa type-IV collagenase compared with untransfected REF. In 2 cell lines the invasive capacity increased during in vitro propagation. The expression of stromelysin-1 increased during this process, whereas 68-kDa type-IV collagenase was persistently expressed at reduced levels. In the third clone analyzed, the invasive capacity decreased during culture, in parallel with decreased expression of stromelysin-1. The low level of stromelysin-1 expression observed in this cell line did not result from loss of AP-1-transcription-factor activity, and was not reversed by phorbol-ester treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenovirus Early Proteins
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cell Transformation, Neoplastic / genetics*
  • Embryo, Mammalian
  • Exons
  • Fibroblasts / metabolism*
  • Fibroblasts / pathology
  • Fibrosarcoma / genetics
  • Fibrosarcoma / pathology
  • Gene Expression
  • Genes, ras*
  • Matrix Metalloproteinase 3
  • Matrix Metalloproteinase 9
  • Metalloendopeptidases / genetics
  • Metalloendopeptidases / metabolism*
  • Microbial Collagenase / genetics
  • Microbial Collagenase / metabolism*
  • Molecular Sequence Data
  • Mutation
  • Neoplasm Metastasis
  • Oncogene Proteins, Viral / genetics*
  • Proto-Oncogene Proteins c-jun / metabolism
  • Rats
  • Transfection

Substances

  • Adenovirus Early Proteins
  • Oncogene Proteins, Viral
  • Proto-Oncogene Proteins c-jun
  • Metalloendopeptidases
  • Matrix Metalloproteinase 3
  • Microbial Collagenase
  • Matrix Metalloproteinase 9