Inhibition of aromatase expression by a psoralen-linked triplex-forming oligonucleotide targeted to a coding sequence

FEBS Lett. 1995 Sep 25;372(2-3):222-8. doi: 10.1016/0014-5793(95)00987-k.

Abstract

The cytochrome P450 enzyme aromatase (P450arom) is an important target in breast cancer treatment. We have designed a 20-base pyrimidine oligodeoxynucleotide (ODN) which forms a sequence-specific triple helix (triplex) with a purine-rich tract in the P450arom coding sequence. The psoralen-linked ODN (Pso20T) formed photo-induced cross-linked products with target double-stranded DNA. Cross-linked adducts formed in vitro between ODNs and P450arom expression constructs were used to transfect COS and human MCF-7 breast cancer cells. Levels of aromatase transcripts and enzyme activity were significantly lower in cultures transfected with Pso20T-treated cDNA relative to controls. Pso20T had a lesser inhibitory effect on aromatase expression from a mutant P450arom construct, consistent with predicted effects of the mutations on triplex formation. These results are compatible with triplex-mediated interruption of transcription within intact cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aromatase / biosynthesis*
  • Base Sequence
  • Binding Sites
  • Ficusin / metabolism*
  • Humans
  • Molecular Sequence Data
  • Oligonucleotides / pharmacology*
  • Protein Synthesis Inhibitors / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Oligonucleotides
  • Protein Synthesis Inhibitors
  • Aromatase
  • Ficusin