Ornithine decarboxylase over-expression stimulates mitogen-activated protein kinase and anchorage-independent growth of human breast epithelial cells

Int J Cancer. 1997 Jan 17;70(2):175-82. doi: 10.1002/(sici)1097-0215(19970117)70:2<175::aid-ijc7>3.0.co;2-u.

Abstract

In these experiments we tested the hypothesis that constitutive activation of polyamine(PA) biosynthesis may contribute to mammary carcinogenesis. Spontaneously immortalized normal human MCF-10A breast epithelial cells were infected with the retroviral vector pLOSN containing a cDNA which codes for a truncated and more stable ornithine decarboxylase (ODC), the rate-limiting enzyme in PA synthesis. Upon chronic selective pressure with alpha-difluoromethyl-ornithine (DFMO) (an irreversible inhibitor of ODC), infected MCF-10A cells exhibited an approximately 250-fold increase in ODC activity, which persisted despite discontinuation of DFMO. ODC-over-expressing MCF-10A cells showed a modest decrease in S-adenosylmethionine decarboxylase and an increase in spermidine/spermineN1-acetyltransferase. Analysis of cellular PA profile revealed a selective accumulation of putrescine without alterations in spermidine and spermine contents. Lesser degrees of increased ODC activity were obtained reproducibly by re-exposing the cells to incremental small doses of DFMO. We observed a bell-shaped dose-related positive effect of ODC activity on clonogenicity in soft agar of MCF-10A cells. Since anchorage-dependent growth was actually reduced, such positive influence on this feature of transformation was not a non-specific consequence of a growth advantage provided by ODC over-expression. In addition, we observed a close parallelism between the dose-dependent effects of ODC expression on clonogenicity and activity of the ERK-2 kinase, a central element of the MAPK cascade. Our data demonstrate an interaction between PA and the MAPK signalling pathway and suggest that the latter may be involved in ODC-induced transformation of mammary epithelial cells.

Publication types

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

MeSH terms

  • Acetyltransferases / metabolism
  • Adenosylmethionine Decarboxylase / metabolism
  • Breast / cytology*
  • Breast / drug effects
  • Breast / enzymology
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic / genetics*
  • Colony-Forming Units Assay
  • DNA, Complementary / genetics
  • Eflornithine / pharmacology
  • Enzyme Induction
  • Epithelial Cells
  • Epithelium / drug effects
  • Epithelium / enzymology
  • Female
  • Genes, ras
  • Humans
  • Mitogen-Activated Protein Kinase 1
  • Ornithine Decarboxylase / biosynthesis
  • Ornithine Decarboxylase / chemistry
  • Ornithine Decarboxylase / genetics
  • Ornithine Decarboxylase / physiology*
  • Ornithine Decarboxylase Inhibitors
  • Polyamines / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction / physiology
  • Transfection

Substances

  • DNA, Complementary
  • Ornithine Decarboxylase Inhibitors
  • Polyamines
  • Recombinant Fusion Proteins
  • Acetyltransferases
  • diamine N-acetyltransferase
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Mitogen-Activated Protein Kinase 1
  • Ornithine Decarboxylase
  • Adenosylmethionine Decarboxylase
  • Eflornithine