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Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells
DNA interstrand cross-links (ICLs) are critical cytotoxic lesions produced by cancer chemotherapeutic agents such as the nitrogen mustards and platinum drugs; however, the exact mechanism of ICL-induced cell death is unclear. Here, we show a novel mechanism of p53-independent apoptotic cell death in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181417/ https://www.ncbi.nlm.nih.gov/pubmed/21814285 http://dx.doi.org/10.1038/cddis.2011.70 |
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author | Osawa, T Davies, D Hartley, J A |
author_facet | Osawa, T Davies, D Hartley, J A |
author_sort | Osawa, T |
collection | PubMed |
description | DNA interstrand cross-links (ICLs) are critical cytotoxic lesions produced by cancer chemotherapeutic agents such as the nitrogen mustards and platinum drugs; however, the exact mechanism of ICL-induced cell death is unclear. Here, we show a novel mechanism of p53-independent apoptotic cell death involving prolonged cell-cycle (G(2)) arrest, ICL repair involving HR, transient mitosis, incomplete cytokinesis, and gross chromosomal abnormalities resulting from ICLs in mammalian cells. This characteristic ‘giant' cell death, observed by using time-lapse video microscopy, was reduced in ICL repair ERCC1- and XRCC3-deficient cells. Collectively, the results illustrate the coordination of ICL-induced cellular responses, including cell-cycle arrest, DNA damage repair, and cell death. |
format | Online Article Text |
id | pubmed-3181417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31814172011-10-20 Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells Osawa, T Davies, D Hartley, J A Cell Death Dis Original Article DNA interstrand cross-links (ICLs) are critical cytotoxic lesions produced by cancer chemotherapeutic agents such as the nitrogen mustards and platinum drugs; however, the exact mechanism of ICL-induced cell death is unclear. Here, we show a novel mechanism of p53-independent apoptotic cell death involving prolonged cell-cycle (G(2)) arrest, ICL repair involving HR, transient mitosis, incomplete cytokinesis, and gross chromosomal abnormalities resulting from ICLs in mammalian cells. This characteristic ‘giant' cell death, observed by using time-lapse video microscopy, was reduced in ICL repair ERCC1- and XRCC3-deficient cells. Collectively, the results illustrate the coordination of ICL-induced cellular responses, including cell-cycle arrest, DNA damage repair, and cell death. Nature Publishing Group 2011-08 2011-08-04 /pmc/articles/PMC3181417/ /pubmed/21814285 http://dx.doi.org/10.1038/cddis.2011.70 Text en Copyright © 2011 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Osawa, T Davies, D Hartley, J A Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells |
title | Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells |
title_full | Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells |
title_fullStr | Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells |
title_full_unstemmed | Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells |
title_short | Mechanism of cell death resulting from DNA interstrand cross-linking in mammalian cells |
title_sort | mechanism of cell death resulting from dna interstrand cross-linking in mammalian cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181417/ https://www.ncbi.nlm.nih.gov/pubmed/21814285 http://dx.doi.org/10.1038/cddis.2011.70 |
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