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Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture
Three-dimensional (3D) cell culture is beneficial for physiological studies of tumor cells, due to its potential to deliver a high quantity of cell culture information that is representative of the cancer microenvironment and predictive of drug responses in vivo. Currently, gel-associated or matrix-...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471796/ https://www.ncbi.nlm.nih.gov/pubmed/25865675 http://dx.doi.org/10.1111/cas.12667 |
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author | Sakamoto, Ruriko Rahman, M Mamunur Shimomura, Manami Itoh, Manabu Nakatsura, Tetsuya |
author_facet | Sakamoto, Ruriko Rahman, M Mamunur Shimomura, Manami Itoh, Manabu Nakatsura, Tetsuya |
author_sort | Sakamoto, Ruriko |
collection | PubMed |
description | Three-dimensional (3D) cell culture is beneficial for physiological studies of tumor cells, due to its potential to deliver a high quantity of cell culture information that is representative of the cancer microenvironment and predictive of drug responses in vivo. Currently, gel-associated or matrix-associated 3D cell culture is comprised of intricate procedures that often result in experimental complexity. Therefore, we developed an innovative anti-cancer drug sensitivity screening technique for 3D cell culture on NanoCulture Plates (NCP) by employing the imaging device BioStation CT. Here, we showed that the human breast cancer cell lines BT474 and T47D form multicellular spheroids on NCP plates and compared their sensitivity to the anti-cancer drugs trastuzumab and paclitaxel using the BioStation CT. The anticancer drugs reduced spheroid migration velocity and suppressed spheroid fusion. In addition, primary cells derived from the human breast cancer tissues B58 and B61 grown on NCP plates also exhibited similar drug sensitivity. These results were in good agreement with the conventional assay method using ATP quantification. We confirmed the antitumor effects of the drugs on cells seeded in 96-well plates using the BioStation CT imaging technique. We expect this method to be useful in research for new antitumor agents and for drug sensitivity tests in individually-tailored cancer treatments. |
format | Online Article Text |
id | pubmed-4471796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44717962015-10-05 Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture Sakamoto, Ruriko Rahman, M Mamunur Shimomura, Manami Itoh, Manabu Nakatsura, Tetsuya Cancer Sci Original Articles Three-dimensional (3D) cell culture is beneficial for physiological studies of tumor cells, due to its potential to deliver a high quantity of cell culture information that is representative of the cancer microenvironment and predictive of drug responses in vivo. Currently, gel-associated or matrix-associated 3D cell culture is comprised of intricate procedures that often result in experimental complexity. Therefore, we developed an innovative anti-cancer drug sensitivity screening technique for 3D cell culture on NanoCulture Plates (NCP) by employing the imaging device BioStation CT. Here, we showed that the human breast cancer cell lines BT474 and T47D form multicellular spheroids on NCP plates and compared their sensitivity to the anti-cancer drugs trastuzumab and paclitaxel using the BioStation CT. The anticancer drugs reduced spheroid migration velocity and suppressed spheroid fusion. In addition, primary cells derived from the human breast cancer tissues B58 and B61 grown on NCP plates also exhibited similar drug sensitivity. These results were in good agreement with the conventional assay method using ATP quantification. We confirmed the antitumor effects of the drugs on cells seeded in 96-well plates using the BioStation CT imaging technique. We expect this method to be useful in research for new antitumor agents and for drug sensitivity tests in individually-tailored cancer treatments. BlackWell Publishing Ltd 2015-06 2015-05-06 /pmc/articles/PMC4471796/ /pubmed/25865675 http://dx.doi.org/10.1111/cas.12667 Text en © 2015 The Authors. Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Sakamoto, Ruriko Rahman, M Mamunur Shimomura, Manami Itoh, Manabu Nakatsura, Tetsuya Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture |
title | Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture |
title_full | Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture |
title_fullStr | Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture |
title_full_unstemmed | Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture |
title_short | Time-lapse imaging assay using the BioStation CT: A sensitive drug-screening method for three-dimensional cell culture |
title_sort | time-lapse imaging assay using the biostation ct: a sensitive drug-screening method for three-dimensional cell culture |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471796/ https://www.ncbi.nlm.nih.gov/pubmed/25865675 http://dx.doi.org/10.1111/cas.12667 |
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