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Inhibiting estrogen responses in breast cancer cells using a fusion protein encoding estrogen receptor-α and the transcriptional repressor PLZF

  • L. Buluwela
  • , J. Pike
  • , D. Mazhar
  • , T. Kamalati
  • , S. M. Hart
  • , R. Al-jehani
  • , H. Yahaya
  • , Nisha Patel
  • , N. Sarwarl
  • , D. A. Heathcote
  • , O. Schwickerath
  • , F. Phoenix
  • , R. Hill
  • , E. Aboagye
  • , S. Shousha
  • , Jonathan Waxman
  • , N. R. Lemoine
  • , A. Zelent
  • , R. Charles Coombes
  • , S. Ali

Research output: Contribution to journalArticlepeer-review

Abstract

Estrogen receptor α (ERα) is a ligand-inducible transcription factor that acts to regulate gene expression by binding to palindromic DNA sequence, known as the estrogen response element, in promoters of estrogen-regulated genes. In breast cancer ERα plays a central role, where estrogen-regulated gene expression leads to tumor initiation, growth and survival. As an approach to silencing estrogen-regulated genes, we have studied the activities of a fusion protein between ERα and the promyelocytic leukemia zinc-finger (PLZF) protein, a transcriptional repressor that acts through chromatin remodeling. To do this, we have developed lines from the estrogen-responsive MCF-7 breast cancer cell line in which the expression of the fusion protein PLZF-ERα is conditionally regulated by tetracycline and shows that these feature long-term silencing of the expression of several well-characterized estrogen-regulated genes, namely pS2, cathepsin-D and the progesterone receptor. However, the estrogen-regulated growth of these cells is not inhibited unless PLZF-ERα expression is induced, an observation that we have confirmed both in vitro and in vivo. Taken together, these results show that PLZF-ERα is a potent repressor of estrogen-regulated gene expression and could be useful in distinguishing estrogen-regulated genes required for the growth of breast cancer cells.
Original languageEnglish
Pages (from-to)452-460
Number of pages9
JournalGene Therapy
Volume12
Issue number5
DOIs
Publication statusPublished - 1 Mar 2005
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • breast cancer
  • estrogen receptor
  • PLZF
  • gene expression

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