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Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library

BACKGROUND: Cancer stem cells (CSCs), a subpopulation in tumors, are known to cause drug resistance, tumor recurrence and metastasis. Based on the characteristic formation of mammospheres in in vitro conditions, the mammosphere formation assay has become an essential tool for quantifying CSC activit...

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Autores principales: Choi, Hack Sun, Kim, Dal-Ah, Chung, Heesung, Park, In Ho, Kim, Bo Hye, Oh, Eok-Soo, Kang, Duk-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307923/
https://www.ncbi.nlm.nih.gov/pubmed/28289331
http://dx.doi.org/10.1186/s12935-017-0392-z
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author Choi, Hack Sun
Kim, Dal-Ah
Chung, Heesung
Park, In Ho
Kim, Bo Hye
Oh, Eok-Soo
Kang, Duk-Hee
author_facet Choi, Hack Sun
Kim, Dal-Ah
Chung, Heesung
Park, In Ho
Kim, Bo Hye
Oh, Eok-Soo
Kang, Duk-Hee
author_sort Choi, Hack Sun
collection PubMed
description BACKGROUND: Cancer stem cells (CSCs), a subpopulation in tumors, are known to cause drug resistance, tumor recurrence and metastasis. Based on the characteristic formation of mammospheres in in vitro conditions, the mammosphere formation assay has become an essential tool for quantifying CSC activity in breast cancer research. However, manual counting of mammospheres is a time-consuming process that is not amenable to high-throughput screening, and there are occasional inaccuracies in the process of determining the mammosphere diameter. In this study, we proposed a novel automated counting method of mammosphere using the National Institute of Standards and Technology (NIST)’s Integrated Colony Enumerator (NICE) with a screening of protein kinase library. METHODS: Human breast cancer cell line MCF-7 was used for evaluation of tumor sphere efficiency, migration, and phenotype transition. Cell viability was assessed using MTT assay, and CSCs were identified by an analysis of CD44 expression and ALDEFLUOR assay using flow cytometry. Automated counting of mammosphere using NICE program was performed with a comparison to the result of manual counting. After identification of inhibitors to ameliorate CSC formation by screening a library of 79 protein kinase inhibitors using automated counting in primary, secondary and tertiary mammosphere assay, the effect of selected kinase inhibitors on migration, colony formation and epithelial-to-mesenchymal transition (EMT) of MCF-7 cells was investigated. RESULTS: Automated counting of mammosphere using NICE program was an easy and less time-consuming process (<1 min for reading 6-well plate) which provided a comparable result with manual counting. Inhibition of calcium/calmodulin-dependent protein kinase II (CaMKII), Janus kinase-3 (JAK-3), and IκB kinase (IKK) were identified to decrease the formation of MCF-7-derived CSCs in primary, secondary and tertiary mammosphere assay. These protein kinase inhibitors alleviated TGF-β1-induced migration, colony formation and EMT of MCF-7 cells. CONCLUSIONS: We have developed a novel automated cell-based screening method which provided an easy, accurate and reproducible way for mammosphere quantification. This study is the first to show the efficacy of an automated medium-throughput mammosphere-counting method in CSC-related research with an identification of protein kinase inhibitors to ameliorate CSC formation.
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spelling pubmed-53079232017-03-13 Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library Choi, Hack Sun Kim, Dal-Ah Chung, Heesung Park, In Ho Kim, Bo Hye Oh, Eok-Soo Kang, Duk-Hee Cancer Cell Int Primary Research BACKGROUND: Cancer stem cells (CSCs), a subpopulation in tumors, are known to cause drug resistance, tumor recurrence and metastasis. Based on the characteristic formation of mammospheres in in vitro conditions, the mammosphere formation assay has become an essential tool for quantifying CSC activity in breast cancer research. However, manual counting of mammospheres is a time-consuming process that is not amenable to high-throughput screening, and there are occasional inaccuracies in the process of determining the mammosphere diameter. In this study, we proposed a novel automated counting method of mammosphere using the National Institute of Standards and Technology (NIST)’s Integrated Colony Enumerator (NICE) with a screening of protein kinase library. METHODS: Human breast cancer cell line MCF-7 was used for evaluation of tumor sphere efficiency, migration, and phenotype transition. Cell viability was assessed using MTT assay, and CSCs were identified by an analysis of CD44 expression and ALDEFLUOR assay using flow cytometry. Automated counting of mammosphere using NICE program was performed with a comparison to the result of manual counting. After identification of inhibitors to ameliorate CSC formation by screening a library of 79 protein kinase inhibitors using automated counting in primary, secondary and tertiary mammosphere assay, the effect of selected kinase inhibitors on migration, colony formation and epithelial-to-mesenchymal transition (EMT) of MCF-7 cells was investigated. RESULTS: Automated counting of mammosphere using NICE program was an easy and less time-consuming process (<1 min for reading 6-well plate) which provided a comparable result with manual counting. Inhibition of calcium/calmodulin-dependent protein kinase II (CaMKII), Janus kinase-3 (JAK-3), and IκB kinase (IKK) were identified to decrease the formation of MCF-7-derived CSCs in primary, secondary and tertiary mammosphere assay. These protein kinase inhibitors alleviated TGF-β1-induced migration, colony formation and EMT of MCF-7 cells. CONCLUSIONS: We have developed a novel automated cell-based screening method which provided an easy, accurate and reproducible way for mammosphere quantification. This study is the first to show the efficacy of an automated medium-throughput mammosphere-counting method in CSC-related research with an identification of protein kinase inhibitors to ameliorate CSC formation. BioMed Central 2017-02-13 /pmc/articles/PMC5307923/ /pubmed/28289331 http://dx.doi.org/10.1186/s12935-017-0392-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Primary Research
Choi, Hack Sun
Kim, Dal-Ah
Chung, Heesung
Park, In Ho
Kim, Bo Hye
Oh, Eok-Soo
Kang, Duk-Hee
Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library
title Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library
title_full Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library
title_fullStr Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library
title_full_unstemmed Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library
title_short Screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library
title_sort screening of breast cancer stem cell inhibitors using a protein kinase inhibitor library
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5307923/
https://www.ncbi.nlm.nih.gov/pubmed/28289331
http://dx.doi.org/10.1186/s12935-017-0392-z
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