Exosomes derived from human bone marrow mesenchymal stem cells promote tumor growth in vivo

Cancer Lett. 2012 Feb 1;315(1):28-37. doi: 10.1016/j.canlet.2011.10.002. Epub 2011 Oct 14.

Abstract

Mesenchymal stem cells (MSCs) can promote tumor growth in a mouse xenograft model, but the exact mechanism remains unclear. In this study, we investigated the effects of bone marrow MSC-derived exosomes (MSC-exosomes) on tumor growth in vitro and in vivo. Our results showed that MSC-exosomes promoted tumor growth in vivo. MSC-exosomes enhanced vascular endothelial growth factor (VEGF) expression in tumor cells by activating extracellular signal-regulated kinase1/2 (ERK1/2) pathway. Inhibition of ERK1/2 activation reserved the increase of VEGF level by MSC-exosomes. Our findings demonstrate a new mechanism through which MSC-exosome-mediated cell-cell interactions may contribute to tumor progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells / cytology*
  • Bone Marrow Cells / metabolism
  • Cell Differentiation / physiology
  • Cell Growth Processes / physiology
  • Exosomes / physiology*
  • Humans
  • Immunohistochemistry
  • Male
  • Mesenchymal Stem Cells / cytology*
  • Mice
  • Mice, Inbred BALB C
  • Neoplasms / pathology*
  • Xenograft Model Antitumor Assays