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3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity

Immunotherapy has emerged as a promising approach to treating several forms of cancer. Use of immune cells, such as natural killer (NK) cells, along with small molecule drugs and antibodies through antibody dependent cell-mediated cytotoxicity (ADCC) has been investigated as a potential combination...

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Autores principales: Gopal, Sneha, Kwon, Seok-Joon, Ku, Bosung, Lee, Dong Woo, Kim, Jungeun, Dordick, Jonathan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295284/
https://www.ncbi.nlm.nih.gov/pubmed/34290356
http://dx.doi.org/10.1038/s42003-021-02417-2
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author Gopal, Sneha
Kwon, Seok-Joon
Ku, Bosung
Lee, Dong Woo
Kim, Jungeun
Dordick, Jonathan S.
author_facet Gopal, Sneha
Kwon, Seok-Joon
Ku, Bosung
Lee, Dong Woo
Kim, Jungeun
Dordick, Jonathan S.
author_sort Gopal, Sneha
collection PubMed
description Immunotherapy has emerged as a promising approach to treating several forms of cancer. Use of immune cells, such as natural killer (NK) cells, along with small molecule drugs and antibodies through antibody dependent cell-mediated cytotoxicity (ADCC) has been investigated as a potential combination therapy for some difficult to treat solid tumors. Nevertheless, there remains a need to develop tools that support co-culture of target cancer cells and effector immune cells in a contextually relevant three-dimensional (3D) environment to provide a rapid means to screen for and optimize ADCC-drug combinations. To that end, here we have developed a high throughput 330 micropillar-microwell sandwich platform that enables 3D co-culture of NK92-CD16 cells with pancreatic (MiaPaCa-2) and breast cancer cell lines (MCF-7 and MDA-MB-231). The platform successfully mimicked hypoxic conditions found in a tumor microenvironment and was used to demonstrate NK-cell mediated cell cytotoxicity in combination with two monoclonal antibodies; Trastuzumab and Atezolizumab. The platform was also used to show dose response behavior of target cancer cells with reduced EC(50) values for paclitaxel (an anti-cancer chemotherapeutic) when treated with both NK cells and antibody. Such a platform may be used to develop more personalized cancer therapies using patient-derived cancer cells.
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spelling pubmed-82952842021-08-12 3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity Gopal, Sneha Kwon, Seok-Joon Ku, Bosung Lee, Dong Woo Kim, Jungeun Dordick, Jonathan S. Commun Biol Article Immunotherapy has emerged as a promising approach to treating several forms of cancer. Use of immune cells, such as natural killer (NK) cells, along with small molecule drugs and antibodies through antibody dependent cell-mediated cytotoxicity (ADCC) has been investigated as a potential combination therapy for some difficult to treat solid tumors. Nevertheless, there remains a need to develop tools that support co-culture of target cancer cells and effector immune cells in a contextually relevant three-dimensional (3D) environment to provide a rapid means to screen for and optimize ADCC-drug combinations. To that end, here we have developed a high throughput 330 micropillar-microwell sandwich platform that enables 3D co-culture of NK92-CD16 cells with pancreatic (MiaPaCa-2) and breast cancer cell lines (MCF-7 and MDA-MB-231). The platform successfully mimicked hypoxic conditions found in a tumor microenvironment and was used to demonstrate NK-cell mediated cell cytotoxicity in combination with two monoclonal antibodies; Trastuzumab and Atezolizumab. The platform was also used to show dose response behavior of target cancer cells with reduced EC(50) values for paclitaxel (an anti-cancer chemotherapeutic) when treated with both NK cells and antibody. Such a platform may be used to develop more personalized cancer therapies using patient-derived cancer cells. Nature Publishing Group UK 2021-07-21 /pmc/articles/PMC8295284/ /pubmed/34290356 http://dx.doi.org/10.1038/s42003-021-02417-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gopal, Sneha
Kwon, Seok-Joon
Ku, Bosung
Lee, Dong Woo
Kim, Jungeun
Dordick, Jonathan S.
3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity
title 3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity
title_full 3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity
title_fullStr 3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity
title_full_unstemmed 3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity
title_short 3D tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity
title_sort 3d tumor spheroid microarray for high-throughput, high-content natural killer cell-mediated cytotoxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295284/
https://www.ncbi.nlm.nih.gov/pubmed/34290356
http://dx.doi.org/10.1038/s42003-021-02417-2
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