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Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells

BACKGROUND: Patients with triple negative breast cancer (TNBC) exhibit poor prognosis and are at high risk of tumour relapse, due to the resistance to chemotherapy. These aggressive phenotypes are in part attributed to the presence of breast cancer stem cells (BCSCs). Therefore, targeting BCSCs is a...

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Autores principales: Tian, Jun, Raffa, Fatmah Al, Dai, Meiou, Moamer, Alaa, Khadang, Baharak, Hachim, Ibrahim Y., Bakdounes, Khldoun, Ali, Suhad, Jean-Claude, Bertrand, Lebrun, Jean-Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288167/
https://www.ncbi.nlm.nih.gov/pubmed/30482914
http://dx.doi.org/10.1038/s41416-018-0287-3
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author Tian, Jun
Raffa, Fatmah Al
Dai, Meiou
Moamer, Alaa
Khadang, Baharak
Hachim, Ibrahim Y.
Bakdounes, Khldoun
Ali, Suhad
Jean-Claude, Bertrand
Lebrun, Jean-Jacques
author_facet Tian, Jun
Raffa, Fatmah Al
Dai, Meiou
Moamer, Alaa
Khadang, Baharak
Hachim, Ibrahim Y.
Bakdounes, Khldoun
Ali, Suhad
Jean-Claude, Bertrand
Lebrun, Jean-Jacques
author_sort Tian, Jun
collection PubMed
description BACKGROUND: Patients with triple negative breast cancer (TNBC) exhibit poor prognosis and are at high risk of tumour relapse, due to the resistance to chemotherapy. These aggressive phenotypes are in part attributed to the presence of breast cancer stem cells (BCSCs). Therefore, targeting BCSCs is a priority to overcoming chemotherapy failure in TNBCs. METHODS: We generated paclitaxel (pac)-resistant TNBC cells which displayed higher sphere forming potential and percentage of BCSC subpopulations compared to the parental cells. A screen with various kinase inhibitors revealed dasatinib, a Src kinase family inhibitor, as a potent suppressor of BCSC expansion/sphere formation in pac-resistant TNBC cells. RESULTS: We found dasatinib to block pac-induced BCSC enrichment and Src activation in both parental and pac-resistant TNBC cells. Interestingly, dasatinib induced an epithelial differentiation of the pac-resistant mesenchymal cells, resulting in their enhanced sensitivity to paclitaxel. The combination treatment of dasatinib and paclitaxel not only decreased the BCSCs numbers and their sphere forming capacity but also synergistically reduced cell viability of pac-resistant cells. Preclinical models of breast cancer further demonstrated the efficiency of the dasatinib/paclitaxel combination treatment in inhibiting tumour growth. CONCLUSIONS: Dasatinib is a promising anti-BCSC drug that could be used in combination with paclitaxel to overcome chemoresistance in TNBC.
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spelling pubmed-62881672019-11-28 Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells Tian, Jun Raffa, Fatmah Al Dai, Meiou Moamer, Alaa Khadang, Baharak Hachim, Ibrahim Y. Bakdounes, Khldoun Ali, Suhad Jean-Claude, Bertrand Lebrun, Jean-Jacques Br J Cancer Article BACKGROUND: Patients with triple negative breast cancer (TNBC) exhibit poor prognosis and are at high risk of tumour relapse, due to the resistance to chemotherapy. These aggressive phenotypes are in part attributed to the presence of breast cancer stem cells (BCSCs). Therefore, targeting BCSCs is a priority to overcoming chemotherapy failure in TNBCs. METHODS: We generated paclitaxel (pac)-resistant TNBC cells which displayed higher sphere forming potential and percentage of BCSC subpopulations compared to the parental cells. A screen with various kinase inhibitors revealed dasatinib, a Src kinase family inhibitor, as a potent suppressor of BCSC expansion/sphere formation in pac-resistant TNBC cells. RESULTS: We found dasatinib to block pac-induced BCSC enrichment and Src activation in both parental and pac-resistant TNBC cells. Interestingly, dasatinib induced an epithelial differentiation of the pac-resistant mesenchymal cells, resulting in their enhanced sensitivity to paclitaxel. The combination treatment of dasatinib and paclitaxel not only decreased the BCSCs numbers and their sphere forming capacity but also synergistically reduced cell viability of pac-resistant cells. Preclinical models of breast cancer further demonstrated the efficiency of the dasatinib/paclitaxel combination treatment in inhibiting tumour growth. CONCLUSIONS: Dasatinib is a promising anti-BCSC drug that could be used in combination with paclitaxel to overcome chemoresistance in TNBC. Nature Publishing Group UK 2018-11-28 2018-12-11 /pmc/articles/PMC6288167/ /pubmed/30482914 http://dx.doi.org/10.1038/s41416-018-0287-3 Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by-nc-sa/4.0/This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License.
spellingShingle Article
Tian, Jun
Raffa, Fatmah Al
Dai, Meiou
Moamer, Alaa
Khadang, Baharak
Hachim, Ibrahim Y.
Bakdounes, Khldoun
Ali, Suhad
Jean-Claude, Bertrand
Lebrun, Jean-Jacques
Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells
title Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells
title_full Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells
title_fullStr Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells
title_full_unstemmed Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells
title_short Dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells
title_sort dasatinib sensitises triple negative breast cancer cells to chemotherapy by targeting breast cancer stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288167/
https://www.ncbi.nlm.nih.gov/pubmed/30482914
http://dx.doi.org/10.1038/s41416-018-0287-3
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