NF-κB p65 and p105 implicate in interleukin 1β-mediated COX-2 expression in melanoma cells

PLoS One. 2018 Dec 18;13(12):e0208955. doi: 10.1371/journal.pone.0208955. eCollection 2018.

Abstract

Inflammatory and microenvironmental factors produced by cancer cells are thought to directly or indirectly promote cancer cell growth. Prostaglandins, including prostaglandin E2, have key roles as a microenvironment factor in influencing the development of tumors, and are produced by the rate limiting enzyme cyclooxygenase 2 (COX-2). In this study, we used canine melanoma cells treated with the proinflammatory cytokine interleukin 1β (IL-1β) and investigated the transcriptional factor nuclear factor-κB (NF-κB) signaling in IL-1β-induced COX-2 expression. IL-1β induced prostaglandin E2 release and COX-2 mRNA expression in a time- and dose-dependent manner. In the cells treated with the NF-κB inhibitors BAY11-7082 and TPC-1, IL-1β-mediated prostaglandin E2 release and COX-2 mRNA expression were inhibited. IL-1β also provoked phosphorylation of p65/RelA and p105/NF-κB1, which are members of the NF-κB families. The IL-1β-induced phosphorylation of p65 and p105 was attenuated in the presence of both NF-κB inhibitors. In melanoma cells transfected with siRNA of p65 or p105, IL-1β-mediated COX-2 mRNA expression was inhibited. These findings suggest that canonical activation of NF-κB signaling plays a crucial role for inflammatory states in melanoma cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Nuclear / genetics*
  • Chromosomal Proteins, Non-Histone / genetics*
  • Cyclooxygenase 2 / genetics*
  • Disease Models, Animal
  • Dogs
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Interleukin-1beta / genetics
  • Melanoma / genetics*
  • Melanoma / pathology
  • Nitriles / pharmacology
  • Phosphorylation / drug effects
  • Signal Transduction / genetics
  • Sulfones / pharmacology
  • Transcription Factor RelA / genetics*

Substances

  • 3-(4-methylphenylsulfonyl)-2-propenenitrile
  • Antigens, Nuclear
  • Chromosomal Proteins, Non-Histone
  • Interleukin-1beta
  • Nitriles
  • P105 antigen, human
  • Sulfones
  • Transcription Factor RelA
  • Cyclooxygenase 2

Grants and funding

This study was funded by the Ministry of Education, Science, Sports, and Culture of Japan (#18K14594) to Rei Nakano and Nihon University Multidisciplinary Research Grant for 2017 (17-019) Tomohiro Nakayama. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.