The S100P/RAGE signaling pathway regulates expression of microRNA-21 in colon cancer cells

FEBS Lett. 2015 Aug 19;589(18):2388-93. doi: 10.1016/j.febslet.2015.07.010. Epub 2015 Jul 17.

Abstract

S100P signaling through the receptor for advanced glycation end-products (RAGE) contributes to colon cancer invasion and metastasis, but the mechanistic features of this process are obscure. Here, we investigate whether activation of S100P/RAGE signaling regulates oncogenic microRNA-21 (miR-21). We show that exogenous S100P up-regulates miR-21 levels in human colon cancer cells, whereas knockdown of S100P results in a decrease of miR-21. Furthermore, blockage of RAGE with anti-RAGE antibody suppresses S100P induction of miR-21. In addition, we found that S100P induction of miR-21 expression involves ERK and is suppressed by the MEK inhibitor U0126. Also, S100P treatment stimulates the enrichment of c-Fos, and AP-1 family members, at the miR-21 gene promoter.

Keywords: AP-1; Colon cancer; Inflammation; Metastasis; RAGE; RECK; TCGA; miR-21; microRNAs.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium-Binding Proteins / metabolism*
  • Cell Line, Tumor
  • Colonic Neoplasms / pathology*
  • Databases, Genetic
  • GPI-Linked Proteins / metabolism
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • MicroRNAs / genetics*
  • Neoplasm Proteins / metabolism*
  • Promoter Regions, Genetic / genetics
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic / metabolism*
  • Signal Transduction*
  • Transcription Factor AP-1 / metabolism
  • Transcription, Genetic
  • Up-Regulation

Substances

  • Calcium-Binding Proteins
  • GPI-Linked Proteins
  • MIRN21 microRNA, human
  • MicroRNAs
  • Neoplasm Proteins
  • RECK protein, human
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic
  • S100P protein, human
  • Transcription Factor AP-1