Mesenchymal stem cells: A promising targeted-delivery vehicle in cancer gene therapy
The targeting drug delivery systems (TDDS) have attracted extensive attention of researchers in recent years. More and more drug/gene targeted delivery carriers, such as liposome, magnetic nanoparticles, ligand-conjugated nanoparticles, microbubbles, etc., have been developed and under investigation...
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Published in | Journal of controlled release Vol. 147; no. 2; pp. 154 - 162 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier B.V
15.10.2010
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | The targeting drug delivery systems (TDDS) have attracted extensive attention of researchers in recent years. More and more drug/gene targeted delivery carriers, such as liposome, magnetic nanoparticles, ligand-conjugated nanoparticles, microbubbles, etc., have been developed and under investigation for their application. However, the currently investigated drug/gene carriers have several disadvantages, which limit their future use in clinical practice. Therefore, design and development of novel drug/gene delivery vehicles has been a hot area of research. Recent studies have shown the ability of mesenchymal stem cells (MSCs) to migrate towards and engraft into the tumor sites, which make them a great hope for efficient targeted-delivery vehicles in cancer gene therapy. In this review article, we examine the promising of using mesenchymal stem cells as a targeted-delivery vehicle for cancer gene therapy, and summarize various challenges and concerns regarding these therapies.
The review describes the potential of using of mesenchymal stem cells as a targeted-delivery vehicle in cancer gene therapy and they mat serve as an effective platform for delivering biological agents into tumors. Schematic of nanocarrier systems and MSCs for site-targeted drug/gene delivery (modified from [5,92]). Folate receptor; EGFR: Epidermal growth factor receptor.
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 ObjectType-Feature-1 |
ISSN: | 0168-3659 1873-4995 |
DOI: | 10.1016/j.jconrel.2010.05.015 |