Resveratrol inhibits LPS-induced epithelial-mesenchymal transition in mouse melanoma model

Innate Immun. 2012 Oct;18(5):685-93. doi: 10.1177/1753425912436589. Epub 2012 Feb 16.

Abstract

Epithelial to mesenchymal transition (EMT) has been linked to metastasis. Resveratrol exhibits potential antitumor activities; however, the inhibitory effects of resveratrol on the EMT of melanoma have not been demonstrated. Here, a new role for LPS in promoting EMT is described. LPS-induced EMT was identified by examining the markers of EMT. To assess the activation of NF-κB signal transduction pathway, we performed a reporter assay by using tumor cells transfected with the luciferase gene under the control of NF-κB response elements. The antitumor effects of resveratrol were evaluated in an experimental mouse metastasis tumor model. LPS increased N-cadherin and Snail expression and decreased zonula occludens-1 expression in a dose- and time-dependent manner. Meanwhile, LPS stimulated cell migration through activation of TLR4/NF-κB signal pathway. LPS-induced EMT is critical for inflammation-initiated metastasis. Nuclear translocation and transcriptional activity of p65 NF-κB, an important inducer of EMT, were inhibited by resveratrol. Resveratrol inhibited LPS-induced tumor migration and markers of EMT, significantly prolonged animal survival and reduced the tumor size. Thus, resveratrol plays an important role in the inhibition of LPS-induced EMT in mouse melanoma through the down-regulation of NF-κB activity. The data provide an insight into the mechanisms on the function of resveratrol during the processes of EMT.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / administration & dosage*
  • Biomarkers, Tumor / metabolism
  • Cadherins / genetics
  • Cadherins / metabolism
  • Disease Models, Animal
  • Epithelial-Mesenchymal Transition / drug effects*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Lipopolysaccharides / metabolism
  • Male
  • Melanoma / drug therapy*
  • Melanoma / secondary
  • Mice
  • Mice, Inbred C3H
  • NF-kappa B / metabolism
  • Resveratrol
  • Signal Transduction
  • Skin Neoplasms / drug therapy*
  • Skin Neoplasms / pathology
  • Snail Family Transcription Factors
  • Stilbenes / administration & dosage*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Antineoplastic Agents, Phytogenic
  • Biomarkers, Tumor
  • Cadherins
  • Lipopolysaccharides
  • NF-kappa B
  • Snail Family Transcription Factors
  • Stilbenes
  • Transcription Factors
  • Resveratrol