RIG-I inhibits the MAPK-dependent proliferation of BRAF mutant melanoma cells via MKP-1

Cell Signal. 2016 May;28(5):335-347. doi: 10.1016/j.cellsig.2016.01.012. Epub 2016 Jan 29.

Abstract

Background: BRAF-mutant melanoma is characterized by aggressive metastatic potential and therapeutic resistance. The innate immune receptor RIG-I has emerged as a potential target in melanoma therapies but the contributing pathways involved in anti-cancer activity are poorly characterized.

Methods: Baseline and ATRA-induced expression of RIG-I in nine (3 wild type and 6 BRAF-mutant) melanoma cell lines was measured with Q-PCR and Western blot. Ligand-specific stimulation of RIG-I was detected by Q-PCR and ELISA. Activation of the RIG-I-coupled IRF3, NF-κB and MAPK pathways was tested with protein array and Western blot. Cell proliferation and apoptosis was monitored by flow cytometry and cell counting. Down modulation of MKP-1 expression in melanoma cells was performed by specific siRNA.

Results: Short-term ATRA pre-treatment increases the expression of RIG-I in BRAF-mutant melanoma cells. Specific activation of RIG-I by 5'ppp-dsRNA leads to increased activity of the IRF3-IFNβ pathway but does not influence NF-κB signaling. RIG-I mediates the targeted dephosphorylation of several MAPKs (p38, RSK1, GSK-3α/β, HSP27) via the endogenous regulator MKP-1 resulting in decreased melanoma cell proliferation.

Conclusion: RIG-I has the potential to exert anticancer activity in BRAF-mutant melanoma via controlling IFNβ production and MAPK signaling. This is the first study showing that RIG-I activation results in MKP-1-mediated inhibition of cell proliferation via controlling the p38-HSP27, c-Jun and rpS6 pathways thus identifying RIG-I and MKP-1 as novel and promising therapeutical targets.

Keywords: BRAF; MAPK; MKP-1/DUSP1; Melanoma; Proliferation; RIG-I.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Proliferation
  • Cytokines / metabolism
  • DEAD Box Protein 58 / metabolism*
  • Dual Specificity Phosphatase 1 / metabolism*
  • Humans
  • Interferon Regulatory Factor-3 / metabolism
  • MAP Kinase Signaling System*
  • Melanoma / enzymology*
  • Melanoma / genetics
  • Melanoma / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Proto-Oncogene Proteins B-raf / genetics*
  • Receptors, Immunologic
  • Tretinoin / pharmacology

Substances

  • Cytokines
  • IRF3 protein, human
  • Interferon Regulatory Factor-3
  • NF-kappa B
  • Receptors, Immunologic
  • Tretinoin
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • Mitogen-Activated Protein Kinases
  • DUSP1 protein, human
  • Dual Specificity Phosphatase 1
  • RIGI protein, human
  • DEAD Box Protein 58