Soluble IL6R represents a miR-34a target: potential implications for the recently identified IL-6R/STAT3/miR-34a feed-back loop

Oncotarget. 2015 Jun 10;6(16):14026-32. doi: 10.18632/oncotarget.4334.

Abstract

We previously reported that IL-6R, STAT3 and miR-34a form a positive feedback-loop, which promotes epithelial to mesenchymal transition (EMT), invasion, and metastasis of colorectal cancer (CRC) [1]. In that study only the membrane-bound form of the IL-6R was shown to be repressed by miR-34a. Here, we show that also the mRNA encoding the soluble IL6R (s-IL-6R) is directly targeted and repressed by miR-34a. Accordingly, the concentration of s-IL6R protein was decreased in conditioned media of CRC cell lines ectopically expressing miR-34a. The s-IL-6R mediates IL-6 trans-signaling, which also affects cells that do not express the IL-6R. Since IL-6 trans-signaling is involved in numerous inflammatory disease states these findings may be relevant for future therapeutic approaches.

Keywords: IL-6R; STAT3; colorectal cancer; inflammation; miR-34a.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Caco-2 Cells
  • Cell Line, Tumor
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology
  • Feedback
  • HT29 Cells
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Receptors, Interleukin-6 / genetics*
  • Receptors, Interleukin-6 / metabolism
  • STAT3 Transcription Factor / genetics*
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction

Substances

  • IL6R protein, human
  • MIRN34 microRNA, human
  • MicroRNAs
  • Receptors, Interleukin-6
  • STAT3 Transcription Factor
  • STAT3 protein, human