miR-98 suppresses melanoma metastasis through a negative feedback loop with its target gene IL-6

Exp Mol Med. 2014 Oct 3;46(10):e116. doi: 10.1038/emm.2014.63.

Abstract

Dysregulated microRNA (miRNA) expression has a critical role in tumor development and metastasis. However, the mechanism by which miRNAs control melanoma metastasis is unknown. Here, we report reduced miR-98 expression in melanoma tissues with increasing tumor stage as well as metastasis; its expression is also negatively associated with melanoma patient survival. Furthermore, we demonstrate that miR-98 inhibits melanoma cell migration in vitro as well as metastatic tumor size in vivo. We also found that IL-6 is a target gene of miR-98, and IL-6 represses miR-98 levels via the Stat3-NF-κB-lin28B pathway. In an in vivo melanoma model, we demonstrate that miR-98 reduces melanoma metastasis and increases survival in part by reducing IL-6 levels; it also decreases Stat3 and p65 phosphorylation as well as lin28B mRNA levels. These results suggest that miR-98 inhibits melanoma metastasis in part through a novel miR-98-IL-6-negative feedback loop.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Down-Regulation
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Interleukin-6 / genetics*
  • Male
  • Melanoma / epidemiology
  • Melanoma / genetics*
  • Melanoma / pathology*
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / genetics*
  • Neoplasm Metastasis / genetics
  • Neoplasm Metastasis / pathology
  • Signal Transduction
  • Survival Analysis

Substances

  • Interleukin-6
  • MIRN98 microRNA, human
  • MIRN98 microRNA, mouse
  • MicroRNAs