Selective regulation of steroid receptor expression in MCF-7 breast cancer cells by a novel member of the heregulin family

Biochem Biophys Res Commun. 1995 Dec 26;217(3):1271-8. doi: 10.1006/bbrc.1995.2905.

Abstract

A 52 kDa heregulin secreted by estrogen receptor (ER)-negative human breast cancer cells induced rapid growth of ER-positive MCF-7 breast cancer cells with a stimulatory effect observed at 10(-11)M. This heregulin down-regulated the message for ER in MCF-7 cells within 24 hours after stimulation. Similarly the ER protein was down-regulated within 24 to 48 hours after stimulation of cells. However, this down-regulation occurred without activation of the ER, since the progesterone receptor (PR) level of cells stimulated with the 52 kDa heregulin did not increase over the time period measured. As a control, estradiol down-regulated and activated ER as shown by a pronounced increase in PR content of MCF-7 cells. This finding indicates an important role of this heregulin in the down-regulation of ER in estrogen-dependent human breast cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / pathology*
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • Genes, fos
  • Genes, myc
  • Glycoproteins / pharmacology*
  • Growth Substances / pharmacology*
  • Humans
  • Neuregulin-1
  • RNA, Messenger / genetics
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism*
  • Receptors, Progesterone / metabolism*
  • Tumor Cells, Cultured

Substances

  • Glycoproteins
  • Growth Substances
  • Neuregulin-1
  • RNA, Messenger
  • Receptors, Estrogen
  • Receptors, Progesterone