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The role of aneuploidy in promoting and suppressing tumors
Impaired mitotic checkpoint signaling can both promote and suppress tumors. The mitotic checkpoint targets Cdc20, the specificity factor of the ubiquitin ligase that promotes anaphase by targeting cyclin B and securin for destruction. In this issue, Li et al. (2009. J. Cell Biol. doi:10.1083/jcb.200...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711620/ https://www.ncbi.nlm.nih.gov/pubmed/19528293 http://dx.doi.org/10.1083/jcb.200905098 |
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author | Weaver, Beth A.A. Cleveland, Don W. |
author_facet | Weaver, Beth A.A. Cleveland, Don W. |
author_sort | Weaver, Beth A.A. |
collection | PubMed |
description | Impaired mitotic checkpoint signaling can both promote and suppress tumors. The mitotic checkpoint targets Cdc20, the specificity factor of the ubiquitin ligase that promotes anaphase by targeting cyclin B and securin for destruction. In this issue, Li et al. (2009. J. Cell Biol. doi:10.1083/jcb.200904020) use gene replacement to produce mice expressing a Cdc20 mutant that cannot be inhibited by the mitotic checkpoint. In addition to the expected aneuploidy, these animals have a high tumor incidence that is likely caused by persistent aneuploidy coupled with nonmitotic functions of mutant Cdc20. |
format | Text |
id | pubmed-2711620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27116202009-12-15 The role of aneuploidy in promoting and suppressing tumors Weaver, Beth A.A. Cleveland, Don W. J Cell Biol Reviews Impaired mitotic checkpoint signaling can both promote and suppress tumors. The mitotic checkpoint targets Cdc20, the specificity factor of the ubiquitin ligase that promotes anaphase by targeting cyclin B and securin for destruction. In this issue, Li et al. (2009. J. Cell Biol. doi:10.1083/jcb.200904020) use gene replacement to produce mice expressing a Cdc20 mutant that cannot be inhibited by the mitotic checkpoint. In addition to the expected aneuploidy, these animals have a high tumor incidence that is likely caused by persistent aneuploidy coupled with nonmitotic functions of mutant Cdc20. The Rockefeller University Press 2009-06-15 /pmc/articles/PMC2711620/ /pubmed/19528293 http://dx.doi.org/10.1083/jcb.200905098 Text en © 2009 Weaver and Cleveland This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Reviews Weaver, Beth A.A. Cleveland, Don W. The role of aneuploidy in promoting and suppressing tumors |
title | The role of aneuploidy in promoting and suppressing tumors |
title_full | The role of aneuploidy in promoting and suppressing tumors |
title_fullStr | The role of aneuploidy in promoting and suppressing tumors |
title_full_unstemmed | The role of aneuploidy in promoting and suppressing tumors |
title_short | The role of aneuploidy in promoting and suppressing tumors |
title_sort | role of aneuploidy in promoting and suppressing tumors |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2711620/ https://www.ncbi.nlm.nih.gov/pubmed/19528293 http://dx.doi.org/10.1083/jcb.200905098 |
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