Chemopreventive effect of oleuropein in colitis-associated colorectal cancer in c57bl/6 mice

Mol Nutr Food Res. 2016 Feb;60(2):242-55. doi: 10.1002/mnfr.201500605. Epub 2015 Oct 26.

Abstract

Scope: The main phenolic secoiridoid oleuropein and active constituent from olive tree (Olea europaea, Oleaceae), has demonstrated anti-inflammatory properties in intestinal inflammation and anti-tumoral effects in different cancer cells. In this study, we evaluated the chemoprevention of oleuropein in a model of azoxymethane (AOM)/Dextran sulfate sodium (DSS)-induced colorectal cancer (CRC) in C57BL/6 mice and the modulatory effect on the Th17 response in DSS acute colitis.

Methods and results: Oleuropein protected from AOM/DSS-induced CRC by improving clinical symptoms, disease activity index score as well as suppressed the growth and multiplicity of colonic tumors. Treatment with oleuropein reduced intestinal IL-6, IFN-γ, TNF-α, and IL-17A concentration, and decreased cyclooxygenase-2, Bax and proliferating cell nuclear antigen protein expression. Western blot analysis also showed a markedly downregulation of CRC-related pathways as nuclear factor-κB (NF-κB), Wnt/β-catenin, phosphatidylinositol-3-kinase (P3IK)/Akt, and signal transducer and activators of transcription (STAT)3. In DSS acute model, oleuropein inhibited Th17 response, by decreasing CD4(+) Rorγt(+) IL-17(+) IFN-γ(+) T-cell subsets in the lamina propria, as well as IL-17A and IFN-γ expression.

Conclusion: Oleuropein as a dietary supplementation could be a promising protective agent against colitis-associated CRC.

Keywords: Azoxymethane/dextran sulphate sodium; Chemoprevention; Colitis-associated colorectal cancer; Oleuropein; Th17 response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology*
  • Azoxymethane / toxicity
  • Cell Proliferation / drug effects
  • Colitis / chemically induced
  • Colitis / complications
  • Colitis / drug therapy*
  • Colon / drug effects*
  • Colon / metabolism
  • Colon / pathology
  • Colorectal Neoplasms / etiology
  • Colorectal Neoplasms / pathology
  • Colorectal Neoplasms / prevention & control*
  • Cytokines / metabolism
  • Dextran Sulfate / toxicity
  • Female
  • Iridoid Glucosides
  • Iridoids / pharmacology*
  • Mice, Inbred C57BL
  • Neoplasms, Experimental / prevention & control
  • Th17 Cells / drug effects

Substances

  • Anticarcinogenic Agents
  • Cytokines
  • Iridoid Glucosides
  • Iridoids
  • oleuropein
  • Dextran Sulfate
  • Azoxymethane