Literature DB >> 23176305

Fetal mesenchymal stem cells in cancer therapy.

Vasiliki Bitsika1, Antonia Vlahou, Maria G Roubelakis.   

Abstract

There is compelling evidence that mesenchymal stem cells (MSCs) can be utilized as delivery vehicles for cancer therapeutics. During the last decade, bone marrow MSCs have been used as delivery vehicles for the local production of therapeutic proteins in multiple tumor types, taking advantage of their innate tropism to the tumor site and their low immunogenicity. More recently, MSCs have been isolated from fetal tissues during gestation or after birth. Fetal MSCs derived from amniotic fluid, amniotic membrane, umbilical cord matrix (Wharton's jelly) and umbilical cord blood are more advantageous than adult MSCs, as they can be isolated noninvasively in large numbers without the ethical reservations associated with embryo research. Several studies have documented that fetal MSCs harbor a therapeutic potential in cancer treatment, as they can home to the tumor site and reduce tumor burden. This natural tumor tropism together with their low immunogenicity renders fetal MSCs as powerful therapeutic tools in gene therapy-based cancer therapeutic schemes. This review summarizes various approaches where the tumor-homing capacity of fetal MSCs has been employed for the localized delivery of anti-tumor therapeutic agents.

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Year:  2013        PMID: 23176305     DOI: 10.2174/1574888x11308020004

Source DB:  PubMed          Journal:  Curr Stem Cell Res Ther        ISSN: 1574-888X            Impact factor:   3.828


  2 in total

1.  Platelet-rich plasma (PRP) promotes fetal mesenchymal stem/stromal cell migration and wound healing process.

Authors:  Maria G Roubelakis; Ourania Trohatou; Apostolos Roubelakis; Evgenia Mili; Ioannis Kalaitzopoulos; Georgios Papazoglou; Kalliopi I Pappa; Nicholas P Anagnou
Journal:  Stem Cell Rev Rep       Date:  2014-06       Impact factor: 5.739

2.  The targeted inhibitory effects of human amniotic fluid stem cells carrying CXCR4 promoter and DAL-1 on non-small cell lung carcinoma growth.

Authors:  L Li; S Li; T Cai; H Wang; X Xie; Z Liu; Y Zhang
Journal:  Gene Ther       Date:  2015-08-17       Impact factor: 5.250

  2 in total

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