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Bioprinting Decellularized Breast Tissue for the Development of Three-Dimensional Breast Cancer Models
[Image: see text] The tumor extracellular matrix (ECM) plays a vital role in tumor progression and drug resistance. Previous studies have shown that breast tissue-derived matrices could be an important biomaterial to recreate the complexity of the tumor ECM. We have developed a method for decellular...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264314/ https://www.ncbi.nlm.nih.gov/pubmed/35735173 http://dx.doi.org/10.1021/acsami.2c00920 |
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author | Blanco-Fernandez, Barbara Rey-Vinolas, Sergi Bağcı, Gülsün Rubi-Sans, Gerard Otero, Jorge Navajas, Daniel Perez-Amodio, Soledad Engel, Elisabeth |
author_facet | Blanco-Fernandez, Barbara Rey-Vinolas, Sergi Bağcı, Gülsün Rubi-Sans, Gerard Otero, Jorge Navajas, Daniel Perez-Amodio, Soledad Engel, Elisabeth |
author_sort | Blanco-Fernandez, Barbara |
collection | PubMed |
description | [Image: see text] The tumor extracellular matrix (ECM) plays a vital role in tumor progression and drug resistance. Previous studies have shown that breast tissue-derived matrices could be an important biomaterial to recreate the complexity of the tumor ECM. We have developed a method for decellularizing and delipidating a porcine breast tissue (TDM) compatible with hydrogel formation. The addition of gelatin methacrylamide and alginate allows this TDM to be bioprinted by itself with good printability, shape fidelity, and cytocompatibility. Furthermore, this bioink has been tuned to more closely recreate the breast tumor by incorporating collagen type I (Col1). Breast cancer cells (BCCs) proliferate in both TDM bioinks forming cell clusters and spheroids. The addition of Col1 improves the printability of the bioink as well as increases BCC proliferation and reduces doxorubicin sensitivity due to a downregulation of HSP90. TDM bioinks also allow a precise three-dimensional printing of scaffolds containing BCCs and stromal cells and could be used to fabricate artificial tumors. Taken together, we have proven that these novel bioinks are good candidates for biofabricating breast cancer models. |
format | Online Article Text |
id | pubmed-9264314 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92643142022-07-09 Bioprinting Decellularized Breast Tissue for the Development of Three-Dimensional Breast Cancer Models Blanco-Fernandez, Barbara Rey-Vinolas, Sergi Bağcı, Gülsün Rubi-Sans, Gerard Otero, Jorge Navajas, Daniel Perez-Amodio, Soledad Engel, Elisabeth ACS Appl Mater Interfaces [Image: see text] The tumor extracellular matrix (ECM) plays a vital role in tumor progression and drug resistance. Previous studies have shown that breast tissue-derived matrices could be an important biomaterial to recreate the complexity of the tumor ECM. We have developed a method for decellularizing and delipidating a porcine breast tissue (TDM) compatible with hydrogel formation. The addition of gelatin methacrylamide and alginate allows this TDM to be bioprinted by itself with good printability, shape fidelity, and cytocompatibility. Furthermore, this bioink has been tuned to more closely recreate the breast tumor by incorporating collagen type I (Col1). Breast cancer cells (BCCs) proliferate in both TDM bioinks forming cell clusters and spheroids. The addition of Col1 improves the printability of the bioink as well as increases BCC proliferation and reduces doxorubicin sensitivity due to a downregulation of HSP90. TDM bioinks also allow a precise three-dimensional printing of scaffolds containing BCCs and stromal cells and could be used to fabricate artificial tumors. Taken together, we have proven that these novel bioinks are good candidates for biofabricating breast cancer models. American Chemical Society 2022-06-23 2022-07-06 /pmc/articles/PMC9264314/ /pubmed/35735173 http://dx.doi.org/10.1021/acsami.2c00920 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Blanco-Fernandez, Barbara Rey-Vinolas, Sergi Bağcı, Gülsün Rubi-Sans, Gerard Otero, Jorge Navajas, Daniel Perez-Amodio, Soledad Engel, Elisabeth Bioprinting Decellularized Breast Tissue for the Development of Three-Dimensional Breast Cancer Models |
title | Bioprinting
Decellularized Breast Tissue for the Development
of Three-Dimensional Breast Cancer Models |
title_full | Bioprinting
Decellularized Breast Tissue for the Development
of Three-Dimensional Breast Cancer Models |
title_fullStr | Bioprinting
Decellularized Breast Tissue for the Development
of Three-Dimensional Breast Cancer Models |
title_full_unstemmed | Bioprinting
Decellularized Breast Tissue for the Development
of Three-Dimensional Breast Cancer Models |
title_short | Bioprinting
Decellularized Breast Tissue for the Development
of Three-Dimensional Breast Cancer Models |
title_sort | bioprinting
decellularized breast tissue for the development
of three-dimensional breast cancer models |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9264314/ https://www.ncbi.nlm.nih.gov/pubmed/35735173 http://dx.doi.org/10.1021/acsami.2c00920 |
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