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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...

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Autores principales: Leiva, Maria Carmen, Garre, Elena, Gustafsson, Anna, Svanström, Andreas, Bogestål, Yalda, Håkansson, Joakim, Ståhlberg, Anders, Landberg, Göran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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