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Tissue Factor promotes breast cancer stem cell activity in vitro
Cancer stem cells (CSCs) are a subpopulation of cells that can self-renew and initiate tumours. The clotting-initiating protein Tissue Factor (TF) promotes metastasis and may be overexpressed in cancer cells with increased CSC activity. We sought to determine whether TF promotes breast CSC activity...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432226/ https://www.ncbi.nlm.nih.gov/pubmed/28033108 http://dx.doi.org/10.18632/oncotarget.13928 |
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author | Shaker, Hudhaifah Harrison, Hannah Clarke, Robert Landberg, Goran Bundred, Nigel J. Versteeg, Henri H. Kirwan, Cliona C. |
author_facet | Shaker, Hudhaifah Harrison, Hannah Clarke, Robert Landberg, Goran Bundred, Nigel J. Versteeg, Henri H. Kirwan, Cliona C. |
author_sort | Shaker, Hudhaifah |
collection | PubMed |
description | Cancer stem cells (CSCs) are a subpopulation of cells that can self-renew and initiate tumours. The clotting-initiating protein Tissue Factor (TF) promotes metastasis and may be overexpressed in cancer cells with increased CSC activity. We sought to determine whether TF promotes breast CSC activity in vitro using human breast cancer cell lines. TF expression was compared in anoikis-resistant (CSC-enriched) and unselected cells. In cells sorted into of TF-expressing and TF-negative (FACS), and in cells transfected to knockdown TF (siRNA) and overexpress TF (cDNA), CSC activity was compared by (i) mammosphere forming efficiency (MFE) (ii) holoclone colony formation (Hc) and (iii) ALDH1 activity. TF expression was increased in anoikis-resistant and high ALDH1-activity T47D cells compared to unselected cells. FACS sorted TF-expressing T47Ds and TF-overexpressing MCF7s had increased CSC activity compared to TF-low cells. TF siRNA cells (MDAMB231, T47D) had reduced CSC activity compared to control cells. FVIIa increased MFE and ALDH1 in a dose-dependent manner (MDAMB231, T47D). The effects of FVIIa on MFE were abrogated by TF siRNA (T47D). Breast CSCs (in vitro) demonstrate increased activity when selected for high TF expression, when induced to overexpress TF, and when stimulated (with FVIIa). Targeting the TF pathway in vivo may abrogate CSC activity. |
format | Online Article Text |
id | pubmed-5432226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-54322262017-05-17 Tissue Factor promotes breast cancer stem cell activity in vitro Shaker, Hudhaifah Harrison, Hannah Clarke, Robert Landberg, Goran Bundred, Nigel J. Versteeg, Henri H. Kirwan, Cliona C. Oncotarget Research Paper Cancer stem cells (CSCs) are a subpopulation of cells that can self-renew and initiate tumours. The clotting-initiating protein Tissue Factor (TF) promotes metastasis and may be overexpressed in cancer cells with increased CSC activity. We sought to determine whether TF promotes breast CSC activity in vitro using human breast cancer cell lines. TF expression was compared in anoikis-resistant (CSC-enriched) and unselected cells. In cells sorted into of TF-expressing and TF-negative (FACS), and in cells transfected to knockdown TF (siRNA) and overexpress TF (cDNA), CSC activity was compared by (i) mammosphere forming efficiency (MFE) (ii) holoclone colony formation (Hc) and (iii) ALDH1 activity. TF expression was increased in anoikis-resistant and high ALDH1-activity T47D cells compared to unselected cells. FACS sorted TF-expressing T47Ds and TF-overexpressing MCF7s had increased CSC activity compared to TF-low cells. TF siRNA cells (MDAMB231, T47D) had reduced CSC activity compared to control cells. FVIIa increased MFE and ALDH1 in a dose-dependent manner (MDAMB231, T47D). The effects of FVIIa on MFE were abrogated by TF siRNA (T47D). Breast CSCs (in vitro) demonstrate increased activity when selected for high TF expression, when induced to overexpress TF, and when stimulated (with FVIIa). Targeting the TF pathway in vivo may abrogate CSC activity. Impact Journals LLC 2016-12-13 /pmc/articles/PMC5432226/ /pubmed/28033108 http://dx.doi.org/10.18632/oncotarget.13928 Text en Copyright: © 2017 Shaker et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Shaker, Hudhaifah Harrison, Hannah Clarke, Robert Landberg, Goran Bundred, Nigel J. Versteeg, Henri H. Kirwan, Cliona C. Tissue Factor promotes breast cancer stem cell activity in vitro |
title | Tissue Factor promotes breast cancer stem cell activity in vitro |
title_full | Tissue Factor promotes breast cancer stem cell activity in vitro |
title_fullStr | Tissue Factor promotes breast cancer stem cell activity in vitro |
title_full_unstemmed | Tissue Factor promotes breast cancer stem cell activity in vitro |
title_short | Tissue Factor promotes breast cancer stem cell activity in vitro |
title_sort | tissue factor promotes breast cancer stem cell activity in vitro |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432226/ https://www.ncbi.nlm.nih.gov/pubmed/28033108 http://dx.doi.org/10.18632/oncotarget.13928 |
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