Inhibition of p185c-erbB-2 proto-oncogene expression by antisense oligodeoxynucleotides down-regulates p185-associated tyrosine-kinase activity and strongly inhibits mammary tumor-cell proliferation

Cancer Gene Ther. 1994 Jun;1(2):99-105.

Abstract

The c-erbB-2 proto-oncogene codes for a 185-kd putative growth factor receptor that is highly homologous to but distinct from the epidermal growth factor (EGF) receptor. Amplification and overexpression of c-erbB-2 occurs in a number of human tumors, in some of which it is a negative prognostic factor. This study investigates the possibility of inhibiting tumor-cell proliferation by blocking c-erbB-2 expression in the human mammary carcinoma cell line SK-Br-3 using chemically modified antisense oligodeoxynucleotides. Expression of the p185c-erbB-2 protein product was selectively reduced within 48 hours and resulted in a growth arrest of SK-Br-3 cells. Biochemical studies of tyrosine-kinase and S6-kinase activities after antisense inhibition of c-erbB-2 show that p185c-erbB-2 activates the S6-kinase signalling pathway in a nonlinear, dose-dependent manner. This may be relevant for the design of therapeutic strategies involving the inhibition of c-erbB-2 (proto)- oncogene expression.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / pathology*
  • Cell Division / drug effects
  • Down-Regulation* / drug effects
  • Gene Amplification
  • Gene Expression Regulation, Neoplastic* / drug effects
  • Humans
  • Molecular Sequence Data
  • Oligonucleotides, Antisense / genetics
  • Oligonucleotides, Antisense / pharmacology*
  • Phosphorylation / drug effects
  • Protein Processing, Post-Translational / drug effects*
  • Proto-Oncogene Mas
  • Proto-Oncogenes* / drug effects
  • Receptor Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Receptor, ErbB-2 / antagonists & inhibitors*
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism
  • Thionucleotides / pharmacology
  • Tumor Cells, Cultured

Substances

  • MAS1 protein, human
  • Oligonucleotides, Antisense
  • Proto-Oncogene Mas
  • Thionucleotides
  • Receptor Protein-Tyrosine Kinases
  • Receptor, ErbB-2