A signal transducer and activator of transcription 3·Nuclear Factor κB (Stat3·NFκB) complex is necessary for the expression of fascin in metastatic breast cancer cells in response to interleukin (IL)-6 and tumor necrosis factor (TNF)-α. Academic Article uri icon

Overview

abstract

  • IL-6 mediated activation of Stat3 is a major signaling pathway in the process of breast cancer metastasis. One important mechanism by which the IL-6/Stat3 pathway promotes metastasis is through transcriptional regulation of the actin-bundling protein fascin. In this study, we further analyzed the transcriptional regulation of the fascin gene promoter. We show that in addition to IL-6, TNF-α increases Stat3 and NFκB binding to the fascin promoter to induce its expression. We also show that NFκB is required for Stat3 recruitment to the fascin promoter in response to IL-6. Furthermore, Stat3 and NFκB form a protein complex in response to cytokine stimulation. Finally, we demonstrate that an overlapping STAT/NFκB site in a highly conserved 160-bp region of the fascin promoter is sufficient and necessary to induce transcription in response to IL-6 and TNF-α.

publication date

  • September 11, 2014

Research

keywords

  • Carrier Proteins
  • Interleukin-6
  • Microfilament Proteins
  • NF-kappa B
  • STAT3 Transcription Factor
  • Tumor Necrosis Factor-alpha

Identity

PubMed Central ID

  • PMC4208015

Scopus Document Identifier

  • 84908424369

Digital Object Identifier (DOI)

  • 10.1074/jbc.M114.591719

PubMed ID

  • 25213863

Additional Document Info

volume

  • 289

issue

  • 43