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Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest
Microtubule inhibitors such as Vinblastine and Paclitaxel are chemotherapy agents that activate the mitotic spindle checkpoint, arresting cells in mitosis and leading to cell death. The pathways that connect mitotic arrest to cell death are not well characterized. We developed a mammalian cell-based...
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Formato: | Texto |
Lenguaje: | English |
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Biological Procedures Online
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1455480/ https://www.ncbi.nlm.nih.gov/pubmed/16799695 http://dx.doi.org/10.1251/bpo116 |
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author | Yamada, Hiroshi Y. Gorbsky, Gary J. |
author_facet | Yamada, Hiroshi Y. Gorbsky, Gary J. |
author_sort | Yamada, Hiroshi Y. |
collection | PubMed |
description | Microtubule inhibitors such as Vinblastine and Paclitaxel are chemotherapy agents that activate the mitotic spindle checkpoint, arresting cells in mitosis and leading to cell death. The pathways that connect mitotic arrest to cell death are not well characterized. We developed a mammalian cell-based cDNA cloning method to isolate proteins and protein fragments whose expression inhibits colony formation in the presence of microtubule inhibitors. Understanding how these proteins impact cellular responses to microtubule drugs will lead to better understanding of the biochemical pathways connecting mitotic arrest and cell death in mammalian cells and may provide novel targets that can enhance microtubule inhibitor-mediated chemotherapy. |
format | Text |
id | pubmed-1455480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Biological Procedures Online |
record_format | MEDLINE/PubMed |
spelling | pubmed-14554802006-06-23 Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest Yamada, Hiroshi Y. Gorbsky, Gary J. Biol Proced Online Research Article Microtubule inhibitors such as Vinblastine and Paclitaxel are chemotherapy agents that activate the mitotic spindle checkpoint, arresting cells in mitosis and leading to cell death. The pathways that connect mitotic arrest to cell death are not well characterized. We developed a mammalian cell-based cDNA cloning method to isolate proteins and protein fragments whose expression inhibits colony formation in the presence of microtubule inhibitors. Understanding how these proteins impact cellular responses to microtubule drugs will lead to better understanding of the biochemical pathways connecting mitotic arrest and cell death in mammalian cells and may provide novel targets that can enhance microtubule inhibitor-mediated chemotherapy. Biological Procedures Online 2006-04-10 /pmc/articles/PMC1455480/ /pubmed/16799695 http://dx.doi.org/10.1251/bpo116 Text en Copyright © April 04, 2006, HY Yamada et al. This paper is Open Access and is published in Biological Procedures Online under license from the authors. Copying, printing, redistribution and storage permitted. |
spellingShingle | Research Article Yamada, Hiroshi Y. Gorbsky, Gary J. Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest |
title | Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest |
title_full | Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest |
title_fullStr | Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest |
title_full_unstemmed | Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest |
title_short | Cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest |
title_sort | cell-based expression cloning for identification of polypeptides that hypersensitize mammalian cells to mitotic arrest |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1455480/ https://www.ncbi.nlm.nih.gov/pubmed/16799695 http://dx.doi.org/10.1251/bpo116 |
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