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Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments
Breast cancer is a heterogeneous disease where the tumor microenvironment, including extracellular components, plays a crucial role in tumor progression, potentially modulating treatment response. Different approaches have been used to develop three‐dimensional models able to recapitulate the comple...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049042/ https://www.ncbi.nlm.nih.gov/pubmed/33368325 http://dx.doi.org/10.1002/jcp.30191 |
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author | Leiva, Maria Carmen Garre, Elena Gustafsson, Anna Svanström, Andreas Bogestål, Yalda Håkansson, Joakim Ståhlberg, Anders Landberg, Göran |
author_facet | Leiva, Maria Carmen Garre, Elena Gustafsson, Anna Svanström, Andreas Bogestål, Yalda Håkansson, Joakim Ståhlberg, Anders Landberg, Göran |
author_sort | Leiva, Maria Carmen |
collection | PubMed |
description | Breast cancer is a heterogeneous disease where the tumor microenvironment, including extracellular components, plays a crucial role in tumor progression, potentially modulating treatment response. Different approaches have been used to develop three‐dimensional models able to recapitulate the complexity of the extracellular matrix. Here, we use cell‐free patient‐derived scaffolds (PDSs) generated from breast cancer samples that were recellularized with cancer cell lines as an in vivo‐like culture system for drug testing. We show that PDS cultured MCF7 cancer cells increased their resistance against the front‐line chemotherapy drugs 5‐fluorouracil, doxorubicin and paclitaxel in comparison to traditional two‐dimensional cell cultures. The gene expression of the environmentally adapted cancer cells was modulated in different ways depending on the drug and the concentration used. High doses of doxorubicin reduced cancer stem cell features, whereas 5‐fluorouracil increased stemness and decreased the proliferative phenotype. By using PDSs repopulated with other breast cancer cell lines, T‐47D and MDA‐MB‐231, we observed both general and cell line specific drug responses. In summary, PDSs can be used to examine the extracellular matrix influence on cancer drug responses and for testing novel compounds in in vivo‐like microenvironments. |
format | Online Article Text |
id | pubmed-8049042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80490422021-04-21 Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments Leiva, Maria Carmen Garre, Elena Gustafsson, Anna Svanström, Andreas Bogestål, Yalda Håkansson, Joakim Ståhlberg, Anders Landberg, Göran J Cell Physiol Original Research Articles Breast cancer is a heterogeneous disease where the tumor microenvironment, including extracellular components, plays a crucial role in tumor progression, potentially modulating treatment response. Different approaches have been used to develop three‐dimensional models able to recapitulate the complexity of the extracellular matrix. Here, we use cell‐free patient‐derived scaffolds (PDSs) generated from breast cancer samples that were recellularized with cancer cell lines as an in vivo‐like culture system for drug testing. We show that PDS cultured MCF7 cancer cells increased their resistance against the front‐line chemotherapy drugs 5‐fluorouracil, doxorubicin and paclitaxel in comparison to traditional two‐dimensional cell cultures. The gene expression of the environmentally adapted cancer cells was modulated in different ways depending on the drug and the concentration used. High doses of doxorubicin reduced cancer stem cell features, whereas 5‐fluorouracil increased stemness and decreased the proliferative phenotype. By using PDSs repopulated with other breast cancer cell lines, T‐47D and MDA‐MB‐231, we observed both general and cell line specific drug responses. In summary, PDSs can be used to examine the extracellular matrix influence on cancer drug responses and for testing novel compounds in in vivo‐like microenvironments. John Wiley and Sons Inc. 2020-12-23 2021-06 /pmc/articles/PMC8049042/ /pubmed/33368325 http://dx.doi.org/10.1002/jcp.30191 Text en © 2020 The Authors. Journal of Cellular Physiology published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Articles Leiva, Maria Carmen Garre, Elena Gustafsson, Anna Svanström, Andreas Bogestål, Yalda Håkansson, Joakim Ståhlberg, Anders Landberg, Göran Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments |
title | Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments |
title_full | Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments |
title_fullStr | Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments |
title_full_unstemmed | Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments |
title_short | Breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments |
title_sort | breast cancer patient‐derived scaffolds as a tool to monitor chemotherapy responses in human tumor microenvironments |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049042/ https://www.ncbi.nlm.nih.gov/pubmed/33368325 http://dx.doi.org/10.1002/jcp.30191 |
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