Modulation of epidermal growth factor receptor in endocrine-resistant, estrogen-receptor-positive breast cancer

Ann N Y Acad Sci. 2002 Jun;963:104-15. doi: 10.1111/j.1749-6632.2002.tb04101.x.

Abstract

An increasing body of evidence demonstrates that growth factor networks are highly interactive with estrogen receptor signaling in the control of breast cancer growth. As such, tumor responses to antihormones are likely to be a composite of the estrogen receptor and growth factor inhibitory activity of these agents. The modulation of growth factor networks during endocrine response is examined, and in vitro and clinical evidence is presented that epidermal growth factor receptor signaling, maintained in either an estrogen receptor-dependent or a receptor-independent manner, is critical to antihormone-resistant breast cancer cell growth. The considerable potential of the epidermal growth factor receptor-selective tyrosine kinase inhibitor Iressa (ZD 1839) to efficiently treat, and perhaps even prevent, endocrine-resistant breast cancer is highlighted.

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents / pharmacology*
  • Breast Neoplasms / metabolism*
  • Cell Division / drug effects
  • Drug Resistance, Neoplasm / physiology*
  • Endocrine Glands
  • ErbB Receptors / metabolism*
  • Estradiol / analogs & derivatives*
  • Estradiol / pharmacology
  • Estrogen Receptor Modulators / pharmacology
  • Female
  • Fulvestrant
  • Gefitinib
  • Humans
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Quinazolines / pharmacology
  • Receptor, ErbB-2 / physiology
  • Receptors, Estrogen / metabolism*
  • Signal Transduction / drug effects*
  • Signal Transduction / physiology
  • Tamoxifen / pharmacology
  • Trastuzumab
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Estrogen Receptor Modulators
  • Quinazolines
  • Receptors, Estrogen
  • Tamoxifen
  • Fulvestrant
  • Estradiol
  • ErbB Receptors
  • Protein-Tyrosine Kinases
  • Receptor, ErbB-2
  • Trastuzumab
  • Gefitinib