Differential effects of extracellular vesicles secreted by mesenchymal stem cells from different sources on glioblastoma cells. (April 2015)
- Record Type:
- Journal Article
- Title:
- Differential effects of extracellular vesicles secreted by mesenchymal stem cells from different sources on glioblastoma cells. (April 2015)
- Main Title:
- Differential effects of extracellular vesicles secreted by mesenchymal stem cells from different sources on glioblastoma cells
- Authors:
- Del Fattore, Andrea
Luciano, Rosa
Saracino, Rossana
Battafarano, Giulia
Rizzo, Cristiano
Pascucci, Luisa
Alessandri, Giulio
Pessina, Augusto
Perrotta, Antonio
Fierabracci, Alessandra
Muraca, Maurizio - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold> <italic>Background:</italic> </bold> Malignant glial tumors, including glioblastoma multiforme, account for 15 – 20% of pediatric CNS malignancies. They are most resistant to therapy and are associated with a poor prognosis.</p> <p> <italic> <bold>Objective:</bold> </italic> Given the ability of mesenchymal stem cells (MSCs) to affect glioma growth, we investigated the effects of extracellular vesicles (EVs) derived from MSCs on U87MG glioblastoma cells line.</p> <p> <bold> <italic>Methods:</italic> </bold> EVs were isolated from culture media of MSCs from different sources, including bone marrow (BM), umbilical cord (UC) and adipose tissue (AT) and added to U87MG culture. The internalization and the effects of BM-, UC- and AT-MSC-EVs on proliferation and apoptosis of tumor cells were evaluated.</p> <p> <bold> <italic>Results:</italic> </bold> Both confocal microscopy and FACS analysis showed internalization of EVs into tumor cells. BM- and UC-MSC-EVs decreased cell proliferation, while an opposite effect was observed with AT-MSC-EVs. Moreover, both BM- and UC-MSC-EVs induced apoptosis of glioblastoma cells, while AT-MSC-EVs had no effect. Loading UC-MSC-EVs with Vincristine further increased cytotoxicity when compared both to the free drug and to untreated EVs.</p> <p> <bold> <italic>Conclusions:</italic> </bold> Different effects of MSC-EVs on cancer cells were observed depending on their tissue of<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold> <italic>Background:</italic> </bold> Malignant glial tumors, including glioblastoma multiforme, account for 15 – 20% of pediatric CNS malignancies. They are most resistant to therapy and are associated with a poor prognosis.</p> <p> <italic> <bold>Objective:</bold> </italic> Given the ability of mesenchymal stem cells (MSCs) to affect glioma growth, we investigated the effects of extracellular vesicles (EVs) derived from MSCs on U87MG glioblastoma cells line.</p> <p> <bold> <italic>Methods:</italic> </bold> EVs were isolated from culture media of MSCs from different sources, including bone marrow (BM), umbilical cord (UC) and adipose tissue (AT) and added to U87MG culture. The internalization and the effects of BM-, UC- and AT-MSC-EVs on proliferation and apoptosis of tumor cells were evaluated.</p> <p> <bold> <italic>Results:</italic> </bold> Both confocal microscopy and FACS analysis showed internalization of EVs into tumor cells. BM- and UC-MSC-EVs decreased cell proliferation, while an opposite effect was observed with AT-MSC-EVs. Moreover, both BM- and UC-MSC-EVs induced apoptosis of glioblastoma cells, while AT-MSC-EVs had no effect. Loading UC-MSC-EVs with Vincristine further increased cytotoxicity when compared both to the free drug and to untreated EVs.</p> <p> <bold> <italic>Conclusions:</italic> </bold> Different effects of MSC-EVs on cancer cells were observed depending on their tissue of origin. Moreover, MSC-EVs can deliver antiblastic drugs to glioblastoma cells.</p> </abstract> … (more)
- Is Part Of:
- Expert opinion on biological therapy. Volume 15:Number 4(2015:Apr.)
- Journal:
- Expert opinion on biological therapy
- Issue:
- Volume 15:Number 4(2015:Apr.)
- Issue Display:
- Volume 15, Issue 4 (2015)
- Year:
- 2015
- Volume:
- 15
- Issue:
- 4
- Issue Sort Value:
- 2015-0015-0004-0000
- Page Start:
- 495
- Page End:
- 504
- Publication Date:
- 2015-04
- Subjects:
- Gene therapy -- Periodicals
Protein drugs -- Periodicals
Peptide drugs -- Periodicals
Immunotherapy -- Periodicals
Drug delivery systems -- Periodicals
615.5 - Journal URLs:
- http://informahealthcare.com/journal/ebt ↗
http://www.ashley-pub.com/loi/ebt ↗
http://www.tandfonline.com/toc/iebt20/current ↗
http://informahealthcare.com ↗
http://miranda.ashley-pub.com/vl=2623054/cl=18/nw=1/rpsv/journal/journal1_home.htm ↗ - DOI:
- 10.1517/14712598.2015.997706 ↗
- Languages:
- English
- ISSNs:
- 1471-2598
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3842.002940
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3114.xml