Neural Regeneration Research ›› 2013, Vol. 8 ›› Issue (22): 2093-2102.doi: 10.3969/j.issn.1673-5374.2013.22.009

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Migration capacity of human umbilical cord mesenchymal stem cells towards glioma in vivo

Cungang Fan, Dongliang Wang, Qingjun Zhang, Jingru Zhou   

  1. Department of Neurosurgery, Peking University People’s Hospital, Beijing 100044, China
  • Received:2013-04-25 Revised:2013-06-30 Online:2013-08-05 Published:2013-08-05
  • Contact: Qingjun Zhang, Chief physician, Professor, Doctoral supervisor, Department of Neurosurgery, Peking University People’s Hospital, Beijing 100044, China, zhangqjhb@ yahoo.com.
  • About author:Cungang Fan, Master, Attending physician, Principal investigator.
  • Supported by:

    国家自然科学基金(No.81001009)。

Abstract:

High-grade glioma is the most common malignant primary brain tumor in adults. The poor prognosis of glioma, combined with a resistance to currently available treatments, necessitates the develop-ment of more effective tumor-selective therapies. Stem cell-based therapies are emerging as novel cell-based delivery vehicle for therapeutic agents. In the present study, we successfully isolated human umbilical cord mesenchymal stem cells by explant culture. The human umbilical cord mesenchymal stem cells were adherent to plastic surfaces, expressed specific surface phenotypes of mesenchymal stem cells as demonstrated by flow cytometry, and possessed multi-differentiation potentials in permissive induction media in vitro. Furthermore, human umbilical cord mesenchymal stem cells demonstrated excellent glioma-specific targeting capacity in established rat glioma models after intratumoral injection or contralateral ventricular administration in vivo. The excellent glioma-specific targeting ability and extensive intratumoral distribution of human umbilical cord mesenchymal stem cells indicate that they may serve as a novel cellular vehicle for delivering therapeutic molecules in glioma therapy.

Key words: neural regeneration, umbilical cord, mesenchymal stem cell, glioma, migration, cell-based therapy, grants-supported paper, neuroregeneration