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Tubulin is a molecular target of the Wnt-activating chemical probe
BACKGROUND: In drug discovery research, cell-based phenotypic screening is an essential method for obtaining potential drug candidates. Revealing the mechanism of action is a key step on the path to drug discovery. However, elucidating the target molecules of hit compounds from phenotypic screening...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873989/ https://www.ncbi.nlm.nih.gov/pubmed/27207629 http://dx.doi.org/10.1186/s12858-016-0066-9 |
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author | Fukuda, Yasunori Sano, Osamu Kazetani, Kenichi Yamamoto, Koji Iwata, Hidehisa Matsui, Junji |
author_facet | Fukuda, Yasunori Sano, Osamu Kazetani, Kenichi Yamamoto, Koji Iwata, Hidehisa Matsui, Junji |
author_sort | Fukuda, Yasunori |
collection | PubMed |
description | BACKGROUND: In drug discovery research, cell-based phenotypic screening is an essential method for obtaining potential drug candidates. Revealing the mechanism of action is a key step on the path to drug discovery. However, elucidating the target molecules of hit compounds from phenotypic screening campaigns remains a difficult and troublesome process. Simple and efficient methods for identifying the target molecules are essential. RESULTS: 2-Amino-4-(3,4-(methylenedioxy)benzylamino)-6-(3-methoxyphenyl)pyrimidine (AMBMP) was identified as a senescence inducer from a phenotypic screening campaign. The compound is widely used as a Wnt agonist, although its target molecules remain to be clarified. To identify its target proteins, we compared a series of cellular assay results for the compound with our pathway profiling database. The database comprises the activities of compounds from simple assays of cellular reporter genes and cellular proliferations. In this database, compounds were classified on the basis of statistical analysis of their activities, which corresponded to a mechanism of action by the representative compounds. In addition, the mechanisms of action of the compounds of interest could be predicted using the database. Based on our database analysis, the compound was anticipated to be a tubulin disruptor, which was subsequently confirmed by its inhibitory activity of tubulin polymerization. CONCLUSION: These results demonstrate that tubulin is identified for the first time as a target molecule of the Wnt-activating small molecule and that this might have misled the conclusions of some previous studies. Moreover, the present study also emphasizes that our pathway profiling database is a simple and potent tool for revealing the mechanisms of action of hit compounds obtained from phenotypic screenings and off targets of chemical probes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12858-016-0066-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4873989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48739892016-05-21 Tubulin is a molecular target of the Wnt-activating chemical probe Fukuda, Yasunori Sano, Osamu Kazetani, Kenichi Yamamoto, Koji Iwata, Hidehisa Matsui, Junji BMC Biochem Research Article BACKGROUND: In drug discovery research, cell-based phenotypic screening is an essential method for obtaining potential drug candidates. Revealing the mechanism of action is a key step on the path to drug discovery. However, elucidating the target molecules of hit compounds from phenotypic screening campaigns remains a difficult and troublesome process. Simple and efficient methods for identifying the target molecules are essential. RESULTS: 2-Amino-4-(3,4-(methylenedioxy)benzylamino)-6-(3-methoxyphenyl)pyrimidine (AMBMP) was identified as a senescence inducer from a phenotypic screening campaign. The compound is widely used as a Wnt agonist, although its target molecules remain to be clarified. To identify its target proteins, we compared a series of cellular assay results for the compound with our pathway profiling database. The database comprises the activities of compounds from simple assays of cellular reporter genes and cellular proliferations. In this database, compounds were classified on the basis of statistical analysis of their activities, which corresponded to a mechanism of action by the representative compounds. In addition, the mechanisms of action of the compounds of interest could be predicted using the database. Based on our database analysis, the compound was anticipated to be a tubulin disruptor, which was subsequently confirmed by its inhibitory activity of tubulin polymerization. CONCLUSION: These results demonstrate that tubulin is identified for the first time as a target molecule of the Wnt-activating small molecule and that this might have misled the conclusions of some previous studies. Moreover, the present study also emphasizes that our pathway profiling database is a simple and potent tool for revealing the mechanisms of action of hit compounds obtained from phenotypic screenings and off targets of chemical probes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12858-016-0066-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-20 /pmc/articles/PMC4873989/ /pubmed/27207629 http://dx.doi.org/10.1186/s12858-016-0066-9 Text en © Fukuda et al. 2016 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 | Research Article Fukuda, Yasunori Sano, Osamu Kazetani, Kenichi Yamamoto, Koji Iwata, Hidehisa Matsui, Junji Tubulin is a molecular target of the Wnt-activating chemical probe |
title | Tubulin is a molecular target of the Wnt-activating chemical probe |
title_full | Tubulin is a molecular target of the Wnt-activating chemical probe |
title_fullStr | Tubulin is a molecular target of the Wnt-activating chemical probe |
title_full_unstemmed | Tubulin is a molecular target of the Wnt-activating chemical probe |
title_short | Tubulin is a molecular target of the Wnt-activating chemical probe |
title_sort | tubulin is a molecular target of the wnt-activating chemical probe |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873989/ https://www.ncbi.nlm.nih.gov/pubmed/27207629 http://dx.doi.org/10.1186/s12858-016-0066-9 |
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