IL-6 secreted by cancer-associated fibroblasts promotes epithelial-mesenchymal transition and metastasis of gastric cancer via JAK2/STAT3 signaling pathway

Oncotarget. 2017 Mar 28;8(13):20741-20750. doi: 10.18632/oncotarget.15119.

Abstract

Cancer-associated fibroblasts (CAFs), as the activated fibroblasts in tumor stroma, are important modifiers of tumor progression. However, the molecular mechanisms underlying the tumor-promoting properties of CAFs in gastric cancer remain unclear. Here, we show that CAFs isolated from gastric cancer produce significant amounts of interleukin-6 (IL-6). CAFs enhances the migration and EMT of gastric cancer cells through the secretion of IL-6 that activates Janus kinase 2/signal transducers and activators of transcription (JAK2/STAT3) pathway in gastric cancer cells, while deprivation of IL-6 using a neutralizing antibody or inhibition of JAK/STAT3 pathway with specific inhibitor AG490 markedly attenuates these phenotypes in gastric cancer cells induced by CAFs. Moreover, silencing IL-6 expression in CAFs or inhibiting JAK2/STAT3 pathway in gastric cancer cells impairs tumor peritoneal metastasis induced by CAFs in vivo. Taken together, these results suggest that CAFs in the tumor microenvironment promote the progression of gastric cancer through IL-6/JAK2/STAT3 signaling, and IL-6 targeted therapy could be a complementary approach against gastric cancer by exerting their action on stromal fibroblasts.

Keywords: JAK/STAT3; cancer-associated fibroblasts; gastric cancer; interleukin-6.

MeSH terms

  • Animals
  • Blotting, Western
  • Cancer-Associated Fibroblasts / metabolism*
  • Cell Line, Tumor
  • Enzyme-Linked Immunosorbent Assay
  • Epithelial-Mesenchymal Transition / physiology*
  • Fluorescent Antibody Technique
  • Heterografts
  • Humans
  • Interleukin-6 / metabolism*
  • Janus Kinase 2 / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Neoplasm Invasiveness / pathology
  • Real-Time Polymerase Chain Reaction
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / physiology
  • Stomach Neoplasms / metabolism
  • Stomach Neoplasms / pathology*
  • Tumor Microenvironment / physiology*

Substances

  • IL6 protein, human
  • Interleukin-6
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • JAK2 protein, human
  • Janus Kinase 2