Bone marrow mesenchymal stem cells ameliorate colitis-associated tumorigenesis in mice

Biochem Biophys Res Commun. 2014 Aug 8;450(4):1402-8. doi: 10.1016/j.bbrc.2014.07.002. Epub 2014 Jul 7.

Abstract

Background and aims: Bone marrow-derived mesenchymal stem cell (MSC) is widely studied in inflammatory bowel disease (IBD) in basic and clinical research. However, patients with IBD have higher risk of developing colorectal cancer and MSC has dual effect on tumorigenesis. This study aims to evaluate the role of MSC on tumorigenesis of IBD.

Methods: MSCs were isolated from the bone marrow of allogenic mice and identified by flow cytometry. Mice in the model of colitis-associated tumorigenesis induced by azoxymethane and dextran sulfate sodium were injected with MSCs. Colon length, spleen size and tumors formation were assessed macroscopically. Pro-inflammatory cytokines and STAT3 phosphorylation in colon tissues were analyzed.

Results: MSCs ameliorated the severity of colitis associated tumorigenesis compared with PBS control, with attenuated weight loss, longer colons and smaller spleens. Tumor number and tumor load were significantly less in the MSC group while tumor size remained comparable. Histological assessment indicated MSCs could reduce histological damage of the colon tissue. Decreased expression of pro-inflammatory cytokines (TNF-α, IL-1β and IL-6), and down-regulation of STAT3 phosphorylation in colon tissue were found after MSC treatment.

Conclusion: MSCs might ameliorate the tumorigenesis of inflammatory bowel disease by suppression of expression of pro-inflammatory cytokines and STAT3 activation.

Keywords: Colitis; Inflammatory bowel disease; Mesenchymal stem cells; Mice; Tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Bone Marrow Cells / cytology*
  • Cells, Cultured
  • Colitis / complications*
  • Colorectal Neoplasms / etiology
  • Colorectal Neoplasms / surgery*
  • Cytokines / metabolism
  • Female
  • Flow Cytometry
  • Inflammation Mediators / metabolism
  • Mesenchymal Stem Cells / chemistry*
  • Mice
  • Mice, Inbred C57BL
  • Phosphorylation
  • Real-Time Polymerase Chain Reaction
  • STAT3 Transcription Factor / metabolism
  • Stem Cell Transplantation*

Substances

  • Cytokines
  • Inflammation Mediators
  • STAT3 Transcription Factor
  • Stat3 protein, mouse