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Different cell fates after mitotic slippage: From aneuploidy to polyploidy
The molecular mechanism responsible for cell fate after mitotic slippage remains unclear. We investigated the different postmitotic effects of aneuploidy versus polyploidy using chemical inhibitors of centromere-associated protein-E (CENP-E) and kinesin family member 11 (KIF11, also known as Eg5). A...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905391/ https://www.ncbi.nlm.nih.gov/pubmed/27308610 http://dx.doi.org/10.1080/23723556.2015.1088503 |
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author | Ohashi, Akihiro |
author_facet | Ohashi, Akihiro |
author_sort | Ohashi, Akihiro |
collection | PubMed |
description | The molecular mechanism responsible for cell fate after mitotic slippage remains unclear. We investigated the different postmitotic effects of aneuploidy versus polyploidy using chemical inhibitors of centromere-associated protein-E (CENP-E) and kinesin family member 11 (KIF11, also known as Eg5). Aneuploidy caused substantial proteotoxic stress and DNA damage accompanied by p53-mediated postmitotic apoptosis, whereas polyploidy did not induce these antiproliferative effects. |
format | Online Article Text |
id | pubmed-4905391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49053912016-10-06 Different cell fates after mitotic slippage: From aneuploidy to polyploidy Ohashi, Akihiro Mol Cell Oncol Author's View The molecular mechanism responsible for cell fate after mitotic slippage remains unclear. We investigated the different postmitotic effects of aneuploidy versus polyploidy using chemical inhibitors of centromere-associated protein-E (CENP-E) and kinesin family member 11 (KIF11, also known as Eg5). Aneuploidy caused substantial proteotoxic stress and DNA damage accompanied by p53-mediated postmitotic apoptosis, whereas polyploidy did not induce these antiproliferative effects. Taylor & Francis 2015-10-06 /pmc/articles/PMC4905391/ /pubmed/27308610 http://dx.doi.org/10.1080/23723556.2015.1088503 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Author's View Ohashi, Akihiro Different cell fates after mitotic slippage: From aneuploidy to polyploidy |
title | Different cell fates after mitotic slippage: From aneuploidy to polyploidy |
title_full | Different cell fates after mitotic slippage: From aneuploidy to polyploidy |
title_fullStr | Different cell fates after mitotic slippage: From aneuploidy to polyploidy |
title_full_unstemmed | Different cell fates after mitotic slippage: From aneuploidy to polyploidy |
title_short | Different cell fates after mitotic slippage: From aneuploidy to polyploidy |
title_sort | different cell fates after mitotic slippage: from aneuploidy to polyploidy |
topic | Author's View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905391/ https://www.ncbi.nlm.nih.gov/pubmed/27308610 http://dx.doi.org/10.1080/23723556.2015.1088503 |
work_keys_str_mv | AT ohashiakihiro differentcellfatesaftermitoticslippagefromaneuploidytopolyploidy |