Cross-talk between signal transducer and activator of transcription 3 and estrogen receptor signaling

Tetsuya Yamamoto, Tadashi Matsuda*, Akira Junicho, Hiroyuki Kishi, Fahri Saatcioglu, Atsushi Muraguchi

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

81 Scopus citations

Abstract

Interleukin-6 (IL-6) is a multifunctional cytokine that plays important roles in the immune system, hematopoiesis, and acute phase reactions. Estrogens have significant roles in a variety of biological events, such as the development and maintenance of female reproductive organs, and bone and lipid metabolism. Previous studies demonstrated that estrogens suppress IL-6-induced osteoporosis and the growth of multiple myeloma cells by repressing IL-6 and IL-6 receptor gene expression. Here we present a novel mechanism for the inhibitory effect of estrogens on IL-6 function. IL-6-induced activation of signal transducer and activator of transcription 3 (STAT3) activity and STAT3-mediated gene expression were suppressed by 17β-estradiol (E2) in breast cancer cells. E2-mediated inhibition of STAT3 activation was reversed by tamoxifen, an estrogen receptor (ER) antagonist. We provide evidence that the inhibitory action of ER on STAT3 activity was due to direct physical interactions between STAT3 and ER which represents a novel form of cross-talk between STAT3 and ER signaling pathways. (C) 2000 Federation of European Biochemical Societies.

Original languageEnglish
Pages (from-to)143-148
Number of pages6
JournalFEBS Letters
Volume486
Issue number2
DOIs
StatePublished - 2000/12/08

Keywords

  • 17β-Estradiol
  • Cross-talk
  • Estrogen receptor
  • Interleukin-6
  • Signal transducer and activator of transcription 3
  • Transcription

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Biochemistry
  • Molecular Biology
  • Genetics
  • Cell Biology

Fingerprint

Dive into the research topics of 'Cross-talk between signal transducer and activator of transcription 3 and estrogen receptor signaling'. Together they form a unique fingerprint.

Cite this