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TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population
BACKGROUND: Tumours contain stem-like, side population (SP) cells, which have increased tumorigenic potential, resistance to traditional therapies and may be responsible for treatment failures and relapse in patients. METHODS: Mesenchymal stem cells (MSCs) were engineered to express the apoptotic li...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994223/ https://www.ncbi.nlm.nih.gov/pubmed/21063402 http://dx.doi.org/10.1038/sj.bjc.6605952 |
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author | Loebinger, M R Sage, E K Davies, D Janes, S M |
author_facet | Loebinger, M R Sage, E K Davies, D Janes, S M |
author_sort | Loebinger, M R |
collection | PubMed |
description | BACKGROUND: Tumours contain stem-like, side population (SP) cells, which have increased tumorigenic potential, resistance to traditional therapies and may be responsible for treatment failures and relapse in patients. METHODS: Mesenchymal stem cells (MSCs) were engineered to express the apoptotic ligand, TNF-related apoptosis-inducing ligand (TRAIL). Squamous (H357) and lung (A549) cancer cell lines were sorted into side and non-side populations (non-SP) by Hoechst flow cytometry. The survival and growth of both SP and non-SP cancer populations, in conjunction with TRAIL-expressing MSCs and mitoxantrone chemotherapy, were assessed by flow cytometry and colony forming ability. RESULTS: Mesenchymal stem cells expressing TRAIL migrate to tumours and reduce the growth of primary cancers and metastases. This report demonstrates that these cells cause apoptosis, death and reduced colony formation of the SP of squamous and adenocarcinoma lung cancer cells and are synergistic when combined with traditional chemotherapy in apoptosis induction. CONCLUSIONS: The sensitivity of putative cancer stem cells to TRAIL-expressing MSCs, suggests their possible role in the prevention of cancer relapse. |
format | Text |
id | pubmed-2994223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-29942232011-11-01 TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population Loebinger, M R Sage, E K Davies, D Janes, S M Br J Cancer Translational Therapeutics BACKGROUND: Tumours contain stem-like, side population (SP) cells, which have increased tumorigenic potential, resistance to traditional therapies and may be responsible for treatment failures and relapse in patients. METHODS: Mesenchymal stem cells (MSCs) were engineered to express the apoptotic ligand, TNF-related apoptosis-inducing ligand (TRAIL). Squamous (H357) and lung (A549) cancer cell lines were sorted into side and non-side populations (non-SP) by Hoechst flow cytometry. The survival and growth of both SP and non-SP cancer populations, in conjunction with TRAIL-expressing MSCs and mitoxantrone chemotherapy, were assessed by flow cytometry and colony forming ability. RESULTS: Mesenchymal stem cells expressing TRAIL migrate to tumours and reduce the growth of primary cancers and metastases. This report demonstrates that these cells cause apoptosis, death and reduced colony formation of the SP of squamous and adenocarcinoma lung cancer cells and are synergistic when combined with traditional chemotherapy in apoptosis induction. CONCLUSIONS: The sensitivity of putative cancer stem cells to TRAIL-expressing MSCs, suggests their possible role in the prevention of cancer relapse. Nature Publishing Group 2010-11 2010-11-09 /pmc/articles/PMC2994223/ /pubmed/21063402 http://dx.doi.org/10.1038/sj.bjc.6605952 Text en Copyright © 2010 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Translational Therapeutics Loebinger, M R Sage, E K Davies, D Janes, S M TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population |
title | TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population |
title_full | TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population |
title_fullStr | TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population |
title_full_unstemmed | TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population |
title_short | TRAIL-expressing mesenchymal stem cells kill the putative cancer stem cell population |
title_sort | trail-expressing mesenchymal stem cells kill the putative cancer stem cell population |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994223/ https://www.ncbi.nlm.nih.gov/pubmed/21063402 http://dx.doi.org/10.1038/sj.bjc.6605952 |
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