Cargando…

Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids

Three-dimensional (3D) cell culture technologies, such as organoids, are physiologically relevant models for basic and clinical applications. Automated microfluidics offers advantages in high-throughput and precision analysis of cells but is not yet compatible with organoids. Here, we present an aut...

Descripción completa

Detalles Bibliográficos
Autores principales: Schuster, Brooke, Junkin, Michael, Kashaf, Sara Saheb, Romero-Calvo, Isabel, Kirby, Kori, Matthews, Jonathan, Weber, Christopher R., Rzhetsky, Andrey, White, Kevin P., Tay, Savaş
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573629/
https://www.ncbi.nlm.nih.gov/pubmed/33077832
http://dx.doi.org/10.1038/s41467-020-19058-4
_version_ 1783597483420549120
author Schuster, Brooke
Junkin, Michael
Kashaf, Sara Saheb
Romero-Calvo, Isabel
Kirby, Kori
Matthews, Jonathan
Weber, Christopher R.
Rzhetsky, Andrey
White, Kevin P.
Tay, Savaş
author_facet Schuster, Brooke
Junkin, Michael
Kashaf, Sara Saheb
Romero-Calvo, Isabel
Kirby, Kori
Matthews, Jonathan
Weber, Christopher R.
Rzhetsky, Andrey
White, Kevin P.
Tay, Savaş
author_sort Schuster, Brooke
collection PubMed
description Three-dimensional (3D) cell culture technologies, such as organoids, are physiologically relevant models for basic and clinical applications. Automated microfluidics offers advantages in high-throughput and precision analysis of cells but is not yet compatible with organoids. Here, we present an automated, high-throughput, microfluidic 3D organoid culture and analysis system to facilitate preclinical research and personalized therapies. Our system provides combinatorial and dynamic drug treatments to hundreds of cultures and enables real-time analysis of organoids. We validate our system by performing individual, combinatorial, and sequential drug screens on human-derived pancreatic tumor organoids. We observe significant differences in the response of individual patient-based organoids to drug treatments and find that temporally-modified drug treatments can be more effective than constant-dose monotherapy or combination therapy in vitro. This integrated platform advances organoids models to screen and mirror real patient treatment courses with potential to facilitate treatment decisions for personalized therapy.
format Online
Article
Text
id pubmed-7573629
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75736292020-10-21 Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids Schuster, Brooke Junkin, Michael Kashaf, Sara Saheb Romero-Calvo, Isabel Kirby, Kori Matthews, Jonathan Weber, Christopher R. Rzhetsky, Andrey White, Kevin P. Tay, Savaş Nat Commun Article Three-dimensional (3D) cell culture technologies, such as organoids, are physiologically relevant models for basic and clinical applications. Automated microfluidics offers advantages in high-throughput and precision analysis of cells but is not yet compatible with organoids. Here, we present an automated, high-throughput, microfluidic 3D organoid culture and analysis system to facilitate preclinical research and personalized therapies. Our system provides combinatorial and dynamic drug treatments to hundreds of cultures and enables real-time analysis of organoids. We validate our system by performing individual, combinatorial, and sequential drug screens on human-derived pancreatic tumor organoids. We observe significant differences in the response of individual patient-based organoids to drug treatments and find that temporally-modified drug treatments can be more effective than constant-dose monotherapy or combination therapy in vitro. This integrated platform advances organoids models to screen and mirror real patient treatment courses with potential to facilitate treatment decisions for personalized therapy. Nature Publishing Group UK 2020-10-19 /pmc/articles/PMC7573629/ /pubmed/33077832 http://dx.doi.org/10.1038/s41467-020-19058-4 Text en © The Author(s) 2020 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
Schuster, Brooke
Junkin, Michael
Kashaf, Sara Saheb
Romero-Calvo, Isabel
Kirby, Kori
Matthews, Jonathan
Weber, Christopher R.
Rzhetsky, Andrey
White, Kevin P.
Tay, Savaş
Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids
title Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids
title_full Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids
title_fullStr Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids
title_full_unstemmed Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids
title_short Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids
title_sort automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7573629/
https://www.ncbi.nlm.nih.gov/pubmed/33077832
http://dx.doi.org/10.1038/s41467-020-19058-4
work_keys_str_mv AT schusterbrooke automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT junkinmichael automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT kashafsarasaheb automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT romerocalvoisabel automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT kirbykori automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT matthewsjonathan automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT weberchristopherr automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT rzhetskyandrey automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT whitekevinp automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids
AT taysavas automatedmicrofluidicplatformfordynamicandcombinatorialdrugscreeningoftumororganoids