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The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis

INTRODUCTION: Understanding the multiple biological functions played by human mesenchymal stem cells (hMSCs) as well as their development as therapeutics in regenerative medicine or in cancer treatment are major fields of research. Indeed, it has been established that hMSCs play a central role in th...

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Autores principales: Kéramidas, Michelle, de Fraipont, Florence, Karageorgis, Anastassia, Moisan, Anaïck, Persoons, Virginie, Richard, Marie-Jeanne, Coll, Jean-Luc, Rome, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706993/
https://www.ncbi.nlm.nih.gov/pubmed/23628074
http://dx.doi.org/10.1186/scrt195
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author Kéramidas, Michelle
de Fraipont, Florence
Karageorgis, Anastassia
Moisan, Anaïck
Persoons, Virginie
Richard, Marie-Jeanne
Coll, Jean-Luc
Rome, Claire
author_facet Kéramidas, Michelle
de Fraipont, Florence
Karageorgis, Anastassia
Moisan, Anaïck
Persoons, Virginie
Richard, Marie-Jeanne
Coll, Jean-Luc
Rome, Claire
author_sort Kéramidas, Michelle
collection PubMed
description INTRODUCTION: Understanding the multiple biological functions played by human mesenchymal stem cells (hMSCs) as well as their development as therapeutics in regenerative medicine or in cancer treatment are major fields of research. Indeed, it has been established that hMSCs play a central role in the pathogenesis and progression of tumours, but their impact on tumour growth remains controversial. METHODS: In this study, we investigated the influence of hMSCs on the growth of pre-established tumours. We engrafted nude mice with luciferase-positive mouse adenocarcinoma cells (TSA-Luc(+)) to obtain subcutaneous or lung tumours. When tumour presence was confirmed by non-invasive bioluminescence imaging, hMSCs were injected into the periphery of the SC tumours or delivered by systemic intravenous injection in mice bearing either SC tumours or lung metastasis. RESULTS: Regardless of the tumour model and mode of hMSC injection, hMSC administration was always associated with decreased tumour growth due to an inhibition of tumour cell proliferation, likely resulting from deep modifications of the tumour angiogenesis. Indeed, we established that although hMSCs can induce the formation of new blood vessels in a non-tumoural cellulose sponge model in mice, they do not modify the overall amount of haemoglobin delivered into the SC tumours or lung metastasis. We observed that these tumour vessels were reduced in number but were longer. CONCLUSIONS: Our results suggest that hMSCs injection decreased solid tumour growth in mice and modified tumour vasculature, which confirms hMSCs could be interesting to use for the treatment of pre-established tumours.
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spelling pubmed-37069932013-07-15 The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis Kéramidas, Michelle de Fraipont, Florence Karageorgis, Anastassia Moisan, Anaïck Persoons, Virginie Richard, Marie-Jeanne Coll, Jean-Luc Rome, Claire Stem Cell Res Ther Research INTRODUCTION: Understanding the multiple biological functions played by human mesenchymal stem cells (hMSCs) as well as their development as therapeutics in regenerative medicine or in cancer treatment are major fields of research. Indeed, it has been established that hMSCs play a central role in the pathogenesis and progression of tumours, but their impact on tumour growth remains controversial. METHODS: In this study, we investigated the influence of hMSCs on the growth of pre-established tumours. We engrafted nude mice with luciferase-positive mouse adenocarcinoma cells (TSA-Luc(+)) to obtain subcutaneous or lung tumours. When tumour presence was confirmed by non-invasive bioluminescence imaging, hMSCs were injected into the periphery of the SC tumours or delivered by systemic intravenous injection in mice bearing either SC tumours or lung metastasis. RESULTS: Regardless of the tumour model and mode of hMSC injection, hMSC administration was always associated with decreased tumour growth due to an inhibition of tumour cell proliferation, likely resulting from deep modifications of the tumour angiogenesis. Indeed, we established that although hMSCs can induce the formation of new blood vessels in a non-tumoural cellulose sponge model in mice, they do not modify the overall amount of haemoglobin delivered into the SC tumours or lung metastasis. We observed that these tumour vessels were reduced in number but were longer. CONCLUSIONS: Our results suggest that hMSCs injection decreased solid tumour growth in mice and modified tumour vasculature, which confirms hMSCs could be interesting to use for the treatment of pre-established tumours. BioMed Central 2013-04-29 /pmc/articles/PMC3706993/ /pubmed/23628074 http://dx.doi.org/10.1186/scrt195 Text en Copyright © 2013 Kéramidas et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kéramidas, Michelle
de Fraipont, Florence
Karageorgis, Anastassia
Moisan, Anaïck
Persoons, Virginie
Richard, Marie-Jeanne
Coll, Jean-Luc
Rome, Claire
The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis
title The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis
title_full The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis
title_fullStr The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis
title_full_unstemmed The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis
title_short The dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis
title_sort dual effect of mesenchymal stem cells on tumour growth and tumour angiogenesis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706993/
https://www.ncbi.nlm.nih.gov/pubmed/23628074
http://dx.doi.org/10.1186/scrt195
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