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Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development
Cancer cell proliferation relies on the ability of cancer cells to grow, transition through the cell cycle, and divide. To identify novel chemical probes for dissecting the mechanisms governing cell cycle progression and cell division, and for developing new anti-cancer therapeutics, we developed an...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237247/ https://www.ncbi.nlm.nih.gov/pubmed/25321469 http://dx.doi.org/10.1038/cddis.2014.420 |
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author | Senese, S Lo, Y C Huang, D Zangle, T A Gholkar, A A Robert, L Homet, B Ribas, A Summers, M K Teitell, M A Damoiseaux, R Torres, J Z |
author_facet | Senese, S Lo, Y C Huang, D Zangle, T A Gholkar, A A Robert, L Homet, B Ribas, A Summers, M K Teitell, M A Damoiseaux, R Torres, J Z |
author_sort | Senese, S |
collection | PubMed |
description | Cancer cell proliferation relies on the ability of cancer cells to grow, transition through the cell cycle, and divide. To identify novel chemical probes for dissecting the mechanisms governing cell cycle progression and cell division, and for developing new anti-cancer therapeutics, we developed and performed a novel cancer cell-based high-throughput chemical screen for cell cycle modulators. This approach identified novel G1, S, G2, and M-phase specific inhibitors with drug-like properties and diverse chemotypes likely targeting a broad array of processes. We further characterized the M-phase inhibitors and highlight the most potent M-phase inhibitor MI-181, which targets tubulin, inhibits tubulin polymerization, activates the spindle assembly checkpoint, arrests cells in mitosis, and triggers a fast apoptotic cell death. Importantly, MI-181 has broad anti-cancer activity, especially against BRAF(V600E) melanomas. |
format | Online Article Text |
id | pubmed-4237247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42372472014-11-26 Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development Senese, S Lo, Y C Huang, D Zangle, T A Gholkar, A A Robert, L Homet, B Ribas, A Summers, M K Teitell, M A Damoiseaux, R Torres, J Z Cell Death Dis Original Article Cancer cell proliferation relies on the ability of cancer cells to grow, transition through the cell cycle, and divide. To identify novel chemical probes for dissecting the mechanisms governing cell cycle progression and cell division, and for developing new anti-cancer therapeutics, we developed and performed a novel cancer cell-based high-throughput chemical screen for cell cycle modulators. This approach identified novel G1, S, G2, and M-phase specific inhibitors with drug-like properties and diverse chemotypes likely targeting a broad array of processes. We further characterized the M-phase inhibitors and highlight the most potent M-phase inhibitor MI-181, which targets tubulin, inhibits tubulin polymerization, activates the spindle assembly checkpoint, arrests cells in mitosis, and triggers a fast apoptotic cell death. Importantly, MI-181 has broad anti-cancer activity, especially against BRAF(V600E) melanomas. Nature Publishing Group 2014-10 2014-10-16 /pmc/articles/PMC4237247/ /pubmed/25321469 http://dx.doi.org/10.1038/cddis.2014.420 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International Licence. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons licence, users will need to obtain permission from the licence holder to reproduce the material. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0 |
spellingShingle | Original Article Senese, S Lo, Y C Huang, D Zangle, T A Gholkar, A A Robert, L Homet, B Ribas, A Summers, M K Teitell, M A Damoiseaux, R Torres, J Z Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development |
title | Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development |
title_full | Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development |
title_fullStr | Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development |
title_full_unstemmed | Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development |
title_short | Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development |
title_sort | chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237247/ https://www.ncbi.nlm.nih.gov/pubmed/25321469 http://dx.doi.org/10.1038/cddis.2014.420 |
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