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High‐throughput screening in colorectal cancer tissue‐originated spheroids
Patient‐derived cancer organoid culture is an important live material that reflects clinical heterogeneity. However, the limited amount of organoids available for each case as well as the considerable amount of time and cost to expand in vitro makes it impractical to perform high‐throughput drug scr...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317944/ https://www.ncbi.nlm.nih.gov/pubmed/30343529 http://dx.doi.org/10.1111/cas.13843 |
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author | Kondo, Jumpei Ekawa, Tomoya Endo, Hiroko Yamazaki, Kanami Tanaka, Norio Kukita, Yoji Okuyama, Hiroaki Okami, Jiro Imamura, Fumio Ohue, Masayuki Kato, Kikuya Nomura, Taisei Kohara, Arihiro Mori, Seiichi Dan, Shingo Inoue, Masahiro |
author_facet | Kondo, Jumpei Ekawa, Tomoya Endo, Hiroko Yamazaki, Kanami Tanaka, Norio Kukita, Yoji Okuyama, Hiroaki Okami, Jiro Imamura, Fumio Ohue, Masayuki Kato, Kikuya Nomura, Taisei Kohara, Arihiro Mori, Seiichi Dan, Shingo Inoue, Masahiro |
author_sort | Kondo, Jumpei |
collection | PubMed |
description | Patient‐derived cancer organoid culture is an important live material that reflects clinical heterogeneity. However, the limited amount of organoids available for each case as well as the considerable amount of time and cost to expand in vitro makes it impractical to perform high‐throughput drug screening using organoid cultures from multiple patients. Here, we report an advanced system for the high‐throughput screening of 2427 drugs using the cancer tissue‐originated spheroid (CTOS) method. In this system, we apply the CTOS method in an ex vivo platform from xenograft tumors, using machines to handle CTOS and reagents, and testing a CTOS reference panel of multiple CTOS lines for the hit drugs. CTOS passages in xenograft tumors resulted in minimal changes of morphological and genomic status, and xenograft tumor generation efficiently expanded the number of CTOS to evaluate multiple drugs. Our panel of colorectal cancer CTOS lines exhibited diverse sensitivities to the hit compounds, demonstrating the usefulness of this system for investigating highly heterogeneous disease. |
format | Online Article Text |
id | pubmed-6317944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63179442019-01-08 High‐throughput screening in colorectal cancer tissue‐originated spheroids Kondo, Jumpei Ekawa, Tomoya Endo, Hiroko Yamazaki, Kanami Tanaka, Norio Kukita, Yoji Okuyama, Hiroaki Okami, Jiro Imamura, Fumio Ohue, Masayuki Kato, Kikuya Nomura, Taisei Kohara, Arihiro Mori, Seiichi Dan, Shingo Inoue, Masahiro Cancer Sci Original Articles Patient‐derived cancer organoid culture is an important live material that reflects clinical heterogeneity. However, the limited amount of organoids available for each case as well as the considerable amount of time and cost to expand in vitro makes it impractical to perform high‐throughput drug screening using organoid cultures from multiple patients. Here, we report an advanced system for the high‐throughput screening of 2427 drugs using the cancer tissue‐originated spheroid (CTOS) method. In this system, we apply the CTOS method in an ex vivo platform from xenograft tumors, using machines to handle CTOS and reagents, and testing a CTOS reference panel of multiple CTOS lines for the hit drugs. CTOS passages in xenograft tumors resulted in minimal changes of morphological and genomic status, and xenograft tumor generation efficiently expanded the number of CTOS to evaluate multiple drugs. Our panel of colorectal cancer CTOS lines exhibited diverse sensitivities to the hit compounds, demonstrating the usefulness of this system for investigating highly heterogeneous disease. John Wiley and Sons Inc. 2018-11-20 2019-01 /pmc/articles/PMC6317944/ /pubmed/30343529 http://dx.doi.org/10.1111/cas.13843 Text en © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Kondo, Jumpei Ekawa, Tomoya Endo, Hiroko Yamazaki, Kanami Tanaka, Norio Kukita, Yoji Okuyama, Hiroaki Okami, Jiro Imamura, Fumio Ohue, Masayuki Kato, Kikuya Nomura, Taisei Kohara, Arihiro Mori, Seiichi Dan, Shingo Inoue, Masahiro High‐throughput screening in colorectal cancer tissue‐originated spheroids |
title | High‐throughput screening in colorectal cancer tissue‐originated spheroids |
title_full | High‐throughput screening in colorectal cancer tissue‐originated spheroids |
title_fullStr | High‐throughput screening in colorectal cancer tissue‐originated spheroids |
title_full_unstemmed | High‐throughput screening in colorectal cancer tissue‐originated spheroids |
title_short | High‐throughput screening in colorectal cancer tissue‐originated spheroids |
title_sort | high‐throughput screening in colorectal cancer tissue‐originated spheroids |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317944/ https://www.ncbi.nlm.nih.gov/pubmed/30343529 http://dx.doi.org/10.1111/cas.13843 |
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