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Live Multicellular Tumor Spheroid Models For High-Content Imaging and Screening In Cancer Drug Discovery
The multi cellular tumor spheroid (MCTS) model has been used for decades with proven superiority over monolayer cell culture models at recapitulating in vivo tumor growth. Yet its use in high-throughput drug discovery has been limited, particularly with image based screening, due to practical and te...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Open
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941083/ https://www.ncbi.nlm.nih.gov/pubmed/24596682 http://dx.doi.org/10.2174/2213988501408010027 |
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author | Reid, Brian G. Jerjian, Taleen Patel, Purvi Zhou, Qiong Yoo, Byong Hoon Kabos, Peter Sartorius, Carol A. LaBarbera, Daniel V. |
author_facet | Reid, Brian G. Jerjian, Taleen Patel, Purvi Zhou, Qiong Yoo, Byong Hoon Kabos, Peter Sartorius, Carol A. LaBarbera, Daniel V. |
author_sort | Reid, Brian G. |
collection | PubMed |
description | The multi cellular tumor spheroid (MCTS) model has been used for decades with proven superiority over monolayer cell culture models at recapitulating in vivo tumor growth. Yet its use in high-throughput drug discovery has been limited, particularly with image based screening, due to practical and technical hurdles. Here we report a significant advance in utilizing live MCTS models for high-content image based drug discovery. Using a validated GFP reporter (CK5Pro-GFP) of luminal breast cancer stem cells (CSC), we developed an algorithm to quantify changes in CK5Pro-GFP expression levels for individual Z-stack planes (local) or as maximal projections of the summed Z-stacks (global) of MCTS. From these image sets, we can quantify the cross-sectional area of GFP positive cells, the fluorescence intensity of the GFP positive cells, and the percent of spheroid cross-sectional area that expresses CK5Pro-GFP.We demonstrate that acquiring data in this manner can be done in real time and is statistically robust (Z’=0.85) for use in primary high-content screening cancer drug discovery. |
format | Online Article Text |
id | pubmed-3941083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-39410832014-03-04 Live Multicellular Tumor Spheroid Models For High-Content Imaging and Screening In Cancer Drug Discovery Reid, Brian G. Jerjian, Taleen Patel, Purvi Zhou, Qiong Yoo, Byong Hoon Kabos, Peter Sartorius, Carol A. LaBarbera, Daniel V. Curr Chem Genom Transl Med Article The multi cellular tumor spheroid (MCTS) model has been used for decades with proven superiority over monolayer cell culture models at recapitulating in vivo tumor growth. Yet its use in high-throughput drug discovery has been limited, particularly with image based screening, due to practical and technical hurdles. Here we report a significant advance in utilizing live MCTS models for high-content image based drug discovery. Using a validated GFP reporter (CK5Pro-GFP) of luminal breast cancer stem cells (CSC), we developed an algorithm to quantify changes in CK5Pro-GFP expression levels for individual Z-stack planes (local) or as maximal projections of the summed Z-stacks (global) of MCTS. From these image sets, we can quantify the cross-sectional area of GFP positive cells, the fluorescence intensity of the GFP positive cells, and the percent of spheroid cross-sectional area that expresses CK5Pro-GFP.We demonstrate that acquiring data in this manner can be done in real time and is statistically robust (Z’=0.85) for use in primary high-content screening cancer drug discovery. Bentham Open 2014-02-07 /pmc/articles/PMC3941083/ /pubmed/24596682 http://dx.doi.org/10.2174/2213988501408010027 Text en © Reid et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Reid, Brian G. Jerjian, Taleen Patel, Purvi Zhou, Qiong Yoo, Byong Hoon Kabos, Peter Sartorius, Carol A. LaBarbera, Daniel V. Live Multicellular Tumor Spheroid Models For High-Content Imaging and Screening In Cancer Drug Discovery |
title | Live Multicellular Tumor Spheroid Models For High-Content Imaging
and Screening In Cancer Drug Discovery |
title_full | Live Multicellular Tumor Spheroid Models For High-Content Imaging
and Screening In Cancer Drug Discovery |
title_fullStr | Live Multicellular Tumor Spheroid Models For High-Content Imaging
and Screening In Cancer Drug Discovery |
title_full_unstemmed | Live Multicellular Tumor Spheroid Models For High-Content Imaging
and Screening In Cancer Drug Discovery |
title_short | Live Multicellular Tumor Spheroid Models For High-Content Imaging
and Screening In Cancer Drug Discovery |
title_sort | live multicellular tumor spheroid models for high-content imaging
and screening in cancer drug discovery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941083/ https://www.ncbi.nlm.nih.gov/pubmed/24596682 http://dx.doi.org/10.2174/2213988501408010027 |
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