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Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells
Conventional 2D cell culture, a traditional tool in pre-clinical studies, can hardly be regarded as a representation of a natural cell microenvironment. In this respect, it might result in altered cellular behaviors. To overcome such a limitation, different approaches have been tested to conduct mor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455496/ https://www.ncbi.nlm.nih.gov/pubmed/33543395 http://dx.doi.org/10.1007/s10439-021-02727-w |
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author | Pasini, Alice Lovecchio, Joseph Cortesi, Marilisa Liverani, Chiara Spadazzi, Chiara Mercatali, Laura Ibrahim, Toni Giordano, Emanuele |
author_facet | Pasini, Alice Lovecchio, Joseph Cortesi, Marilisa Liverani, Chiara Spadazzi, Chiara Mercatali, Laura Ibrahim, Toni Giordano, Emanuele |
author_sort | Pasini, Alice |
collection | PubMed |
description | Conventional 2D cell culture, a traditional tool in pre-clinical studies, can hardly be regarded as a representation of a natural cell microenvironment. In this respect, it might result in altered cellular behaviors. To overcome such a limitation, different approaches have been tested to conduct more representative in vitro studies. In particular, the use of 3D cell culture introduces variables, such as cell-cell and cell-extracellular matrix interactions; cell features such as survival, proliferation and migration are consequently influenced. For an example, an enhanced drug resistance and increased invasiveness are shown by cancer cells when cultured in 3D versus 2D conventional culture models. In this setting however, non-uniform cell distribution and biological behaviors appear throughout the scaffold, due to reduced diffusion of oxygen and nutrients. Perfusion in bioreactor systems can be used to improve medium transport. In this line of reasoning, this study proposes a breast cancer cell culture model sustained by an integrated approach that couples a 3D environment and a fluid perfusion. This model improves viability and uniformness of cell distribution, while inducing morphological, functional and molecular cancer cell remodeling. |
format | Online Article Text |
id | pubmed-8455496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-84554962021-10-07 Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells Pasini, Alice Lovecchio, Joseph Cortesi, Marilisa Liverani, Chiara Spadazzi, Chiara Mercatali, Laura Ibrahim, Toni Giordano, Emanuele Ann Biomed Eng Original Article Conventional 2D cell culture, a traditional tool in pre-clinical studies, can hardly be regarded as a representation of a natural cell microenvironment. In this respect, it might result in altered cellular behaviors. To overcome such a limitation, different approaches have been tested to conduct more representative in vitro studies. In particular, the use of 3D cell culture introduces variables, such as cell-cell and cell-extracellular matrix interactions; cell features such as survival, proliferation and migration are consequently influenced. For an example, an enhanced drug resistance and increased invasiveness are shown by cancer cells when cultured in 3D versus 2D conventional culture models. In this setting however, non-uniform cell distribution and biological behaviors appear throughout the scaffold, due to reduced diffusion of oxygen and nutrients. Perfusion in bioreactor systems can be used to improve medium transport. In this line of reasoning, this study proposes a breast cancer cell culture model sustained by an integrated approach that couples a 3D environment and a fluid perfusion. This model improves viability and uniformness of cell distribution, while inducing morphological, functional and molecular cancer cell remodeling. Springer International Publishing 2021-02-04 2021 /pmc/articles/PMC8455496/ /pubmed/33543395 http://dx.doi.org/10.1007/s10439-021-02727-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Pasini, Alice Lovecchio, Joseph Cortesi, Marilisa Liverani, Chiara Spadazzi, Chiara Mercatali, Laura Ibrahim, Toni Giordano, Emanuele Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells |
title | Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells |
title_full | Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells |
title_fullStr | Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells |
title_full_unstemmed | Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells |
title_short | Perfusion Flow Enhances Viability and Migratory Phenotype in 3D-Cultured Breast Cancer Cells |
title_sort | perfusion flow enhances viability and migratory phenotype in 3d-cultured breast cancer cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455496/ https://www.ncbi.nlm.nih.gov/pubmed/33543395 http://dx.doi.org/10.1007/s10439-021-02727-w |
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