Spontaneous transformation of adult mesenchymal stem cells from cynomolgus macaques in vitro

Exp Cell Res. 2011 Dec 10;317(20):2950-7. doi: 10.1016/j.yexcr.2011.09.008. Epub 2011 Sep 22.

Abstract

Mesenchymal stem cells (MSCs) have shown potential clinical utility in cell therapy and tissue engineering, due to their ability to proliferate as well as to differentiate into multiple lineages, including osteogenic, adipogenic, and chondrogenic specifications. Therefore, it is crucial to assess the safety of MSCs while extensive expansion ex vivo is a prerequisite to obtain the cell numbers for cell transplantation. Here we show that MSCs derived from adult cynomolgus monkey can undergo spontaneous transformation following in vitro culture. In comparison with MSCs, the spontaneously transformed mesenchymal cells (TMCs) display significantly different growth pattern and morphology, reminiscent of the characteristics of tumor cells. Importantly, TMCs are highly tumorigenic, causing subcutaneous tumors when injected into NOD/SCID mice. Moreover, no multiple differentiation potential of TMCs is observed in vitro or in vivo, suggesting that spontaneously transformed adult stem cells may not necessarily turn into cancer stem cells. These data indicate a direct transformation of cynomolgus monkey MSCs into tumor cells following long-term expansion in vitro. The spontaneous transformation of the cultured cynomolgus monkey MSCs may have important implications for ongoing clinical trials and for models of oncogenesis, thus warranting a more strict assessment of MSCs prior to cell therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult Stem Cells / pathology*
  • Animals
  • Antigens, Surface / genetics
  • Cell Differentiation / physiology
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / pathology*
  • Karyotype
  • Macaca
  • Macaca fascicularis
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / pathology*
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Telomerase / metabolism

Substances

  • Antigens, Surface
  • Telomerase