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Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient

Performing drug screening of tissue derived from cancer patient biopsies using physiologically relevant 3D tumour models presents challenges due to the limited amount of available cell material. Here, we present a microfluidic platform that enables drug screening of cancer cell-enriched multicellula...

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Autores principales: Mulholland, Theresa, McAllister, Milly, Patek, Samantha, Flint, David, Underwood, Mark, Sim, Alexander, Edwards, Joanne, Zagnoni, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168499/
https://www.ncbi.nlm.nih.gov/pubmed/30279484
http://dx.doi.org/10.1038/s41598-018-33055-0
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author Mulholland, Theresa
McAllister, Milly
Patek, Samantha
Flint, David
Underwood, Mark
Sim, Alexander
Edwards, Joanne
Zagnoni, Michele
author_facet Mulholland, Theresa
McAllister, Milly
Patek, Samantha
Flint, David
Underwood, Mark
Sim, Alexander
Edwards, Joanne
Zagnoni, Michele
author_sort Mulholland, Theresa
collection PubMed
description Performing drug screening of tissue derived from cancer patient biopsies using physiologically relevant 3D tumour models presents challenges due to the limited amount of available cell material. Here, we present a microfluidic platform that enables drug screening of cancer cell-enriched multicellular spheroids derived from tumour biopsies, allowing extensive anticancer compound screening prior to treatment. This technology was validated using cell lines and then used to screen primary human prostate cancer cells, grown in 3D as a heterogeneous culture from biopsy-derived tissue. The technology enabled the formation of repeatable drug concentration gradients across an array of spheroids without external fluid actuation, delivering simultaneously a range of drug concentrations to multiple sized spheroids, as well as replicates for each concentration. As proof-of-concept screening, spheroids were generated from two patient biopsies and a panel of standard-of-care compounds for prostate cancer were tested. Brightfield and fluorescence images were analysed to provide readouts of spheroid growth and health, as well as drug efficacy over time. Overall, this technology could prove a useful tool for personalised medicine and future drug development, with the potential to provide cost- and time-reduction in the healthcare delivery.
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spelling pubmed-61684992018-10-05 Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient Mulholland, Theresa McAllister, Milly Patek, Samantha Flint, David Underwood, Mark Sim, Alexander Edwards, Joanne Zagnoni, Michele Sci Rep Article Performing drug screening of tissue derived from cancer patient biopsies using physiologically relevant 3D tumour models presents challenges due to the limited amount of available cell material. Here, we present a microfluidic platform that enables drug screening of cancer cell-enriched multicellular spheroids derived from tumour biopsies, allowing extensive anticancer compound screening prior to treatment. This technology was validated using cell lines and then used to screen primary human prostate cancer cells, grown in 3D as a heterogeneous culture from biopsy-derived tissue. The technology enabled the formation of repeatable drug concentration gradients across an array of spheroids without external fluid actuation, delivering simultaneously a range of drug concentrations to multiple sized spheroids, as well as replicates for each concentration. As proof-of-concept screening, spheroids were generated from two patient biopsies and a panel of standard-of-care compounds for prostate cancer were tested. Brightfield and fluorescence images were analysed to provide readouts of spheroid growth and health, as well as drug efficacy over time. Overall, this technology could prove a useful tool for personalised medicine and future drug development, with the potential to provide cost- and time-reduction in the healthcare delivery. Nature Publishing Group UK 2018-10-02 /pmc/articles/PMC6168499/ /pubmed/30279484 http://dx.doi.org/10.1038/s41598-018-33055-0 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mulholland, Theresa
McAllister, Milly
Patek, Samantha
Flint, David
Underwood, Mark
Sim, Alexander
Edwards, Joanne
Zagnoni, Michele
Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient
title Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient
title_full Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient
title_fullStr Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient
title_full_unstemmed Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient
title_short Drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient
title_sort drug screening of biopsy-derived spheroids using a self-generated microfluidic concentration gradient
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168499/
https://www.ncbi.nlm.nih.gov/pubmed/30279484
http://dx.doi.org/10.1038/s41598-018-33055-0
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