Prostate-specific IL-6 transgene autonomously induce prostate neoplasm through amplifying inflammation in the prostate and peri-prostatic adipose tissue

J Hematol Oncol. 2017 Jan 11;10(1):14. doi: 10.1186/s13045-016-0386-7.

Abstract

Background: The causative role of the pro-inflammatory cytokine IL-6 in prostate cancer progression has been well established at molecular level. However, whether and how IL-6 may play a role in prostate cancer risk and development is not well defined. One limitation factor to acquiring this knowledge is the lack of appropriate animal models.

Methods: We generated a novel line of prostate-specific IL-6 transgenic mouse model. We compared the prostate pathology, tumorigenic signaling components, and prostate tumor microenvironment of the IL-6 transgenic mice with wild type littermates.

Results: With this model, we demonstrate that IL-6 induces prostate neoplasm autonomously. We further demonstrate that transgenic expression of IL-6 in the prostate activates oncogenic pathways, induces autocrine IL-6 secretion and steadily-state of STAT3 activation in the prostate tissue, upregulates paracrine insulin-like growth factor (IGF) signaling axis, reprograms prostate oncogenic gene expression, and more intriguingly, amplifies inflammation in the prostate and peri-prostatic adipose tissue.

Conclusions: The pro-inflammatory IL-6 is autonomous oncogene for the prostate. IL-6 induces prostate oncogenesis through amplifying local inflammation. We also presented a valuable animal model to study inflammation and prostate cancer development.

Keywords: IL-6; Inflammation; Prostate neoplasm; Transgenic mouse.

MeSH terms

  • Adipose Tissue / pathology
  • Animals
  • Cell Transformation, Neoplastic
  • Disease Models, Animal*
  • Inflammation / chemically induced*
  • Insulin-Like Growth Factor I / metabolism
  • Interleukin-6 / genetics*
  • Interleukin-6 / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • Oncogenes
  • Prostate / pathology
  • Prostatic Neoplasms / chemically induced*
  • Prostatic Neoplasms / pathology
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • Transgenes

Substances

  • Interleukin-6
  • STAT3 Transcription Factor
  • interleukin-6, mouse
  • Insulin-Like Growth Factor I