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Inhibition of intracranial glioma growth by endometrial regenerative cells

Xiaodi Han, Xiaolong Meng, Zhenglian Yin, Andrea Rogers, Jie Zhong, Paul Rillema, James A. Jackson, Thomas E. Ichim, Boris Minev, Ewa Carrier, Amit N. Patel, Michael P. Murphy, Wei-Ping Min and Neil H. Riordan
Volume 8, Issue 4
February 15, 2009
Pages 606 - 610

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Animal studies have demonstrated that selective tropism of mesenchymal stem cells (MSC) for glioma may be used as a means of selective delivery of cytotoxic payloads.  Endometrial Regenerative Cells (ERC) are a population of mesenchymal-like cells which possesse pluripotent differentiation capacity and is characterized by unique surface markers and growth factor production.  In this study we sought to determine whether unmanipulated ERC would alter the growth of glioma using the aggressive C6/LacZ7 (C6) into Sprague Dawley rat model.  ERC administration by intravenous (i.v.) or intratumoral (i.t.) showed significant inhibition of glioma: volume reduction of 49% after i.v. treatment (p<0.05), and about 46% i.t. treatment (p<0.05). Tumor reduction was associated with inhibition of angiogenesis and reduced numbers of CD133 positive cells in the incranial tumor.  Despite the angiogenic potential of ERC in the hindlimb ischemia model, these data support a paradoxical tumor inhibitory activity of ERC.  Further studies are needed to determine the qualitative differences between physiological angiogenesis, which seems to be supported by ERC and tumor angiogenesis which appeared to be inhibited.


Authors

Xiaodi Han
Bio-Communications Research Institute; Wichita, Kansas
Xiaolong Meng
Bio-Communications Research Institute; Wichita, Kansas
Zhenglian Yin
Bio-Communications Research Institute; Wichita, Kansas
Andrea Rogers
Bio-Communications Research Institute; Wichita, Kansas
Jie Zhong
Bio-Communications Research Institute; Wichita, Kansas
Paul Rillema
Wichita State University; Wichita, Kansas
James A. Jackson
Bio-Communication Research Institute; Wichita, Kansas
Thomas E. Ichim Corresponding author: Thomas.ichim@gmail.com
Medistem Inc.; San Diego, CA
Boris Minev
Moores UCSD Cancer Centre; San Diego, CA
Ewa Carrier
Moores UCSD Cancer Centre; San Diego, CA
Amit N. Patel
University of Utah; Salt Lake City, UT
Michael P. Murphy
Indiana University School of Medicine; Indianapolis, IN
Wei-Ping Min
University of Western Ontario; Ontario, Canada
Neil H. Riordan
Bio-Communications Research Institute; Wichita, Kansas

We now provide open access to journal articles published online for one year or more. This article may be downloaded at the following link:

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If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.

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