Toll-like receptor 9 agonists promote IL-8 and TGF-beta1 production via activation of nuclear factor kappaB in PC-3 cells

Cancer Genet Cytogenet. 2009 Jul 15;192(2):60-7. doi: 10.1016/j.cancergencyto.2009.03.006.

Abstract

Chronic infection and resulting inflammation promote tumor development and progression, and Toll-like receptors (TLRs) may play an important role in this process. The aim of this study was to determine whether CpG oligonucleotides (CpG-ODN), which are Toll-like receptor 9 (TLR9) agonists, can promote inflammatory cytokines release from the prostate cancer PC-3 cells through activation of nuclear factor-kappaB (NF-kappaB). Flow cytometry, semiquantitative real-time reverse transcriptase-polymerase chain reaction, enzyme-linked immunosorbent assay, and immunofluorescence analysis were used to detect the transforming growth factor-beta1 (TGF-beta1) and interleukin-8 (IL-8) release and NF-kappaB activation in PC-3 cells after CpG-ODN stimulation. CpG-ODN promoted the expression and secretion of immunosuppressive cytokines TGF-beta1 and IL-8 from PC-3 cells. In addition, after CpG-ODN stimulation, NF-kappaB nuclear translocation was also observed in PC-3 cells, contributing to CpG-induced upregulation of IL-8 and TGF-beta1. Thus, TLR9 agonists may promote IL-8 and TGF-beta1 production in human prostate cancer cells through NF-kappaB activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Chloroquine / pharmacology
  • Humans
  • Interleukin-8 / biosynthesis*
  • Male
  • NF-kappa B / metabolism*
  • Oligodeoxyribonucleotides / pharmacology*
  • Proline / analogs & derivatives
  • Proline / pharmacology
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology*
  • Protein Transport / drug effects
  • Signal Transduction / drug effects
  • Thiocarbamates / pharmacology
  • Toll-Like Receptor 9 / agonists*
  • Toll-Like Receptor 9 / metabolism
  • Transforming Growth Factor beta1 / biosynthesis*

Substances

  • CPG-oligonucleotide
  • Interleukin-8
  • NF-kappa B
  • Oligodeoxyribonucleotides
  • Thiocarbamates
  • Toll-Like Receptor 9
  • Transforming Growth Factor beta1
  • prolinedithiocarbamate
  • Chloroquine
  • Proline