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Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis
Checkpoint kinase 1 (CHK1) is critical for intrinsic cell cycle control and coordination of cell cycle progression in response to DNA damage. Despite its essential function, CHK1 has been identified as a target to kill cancer cells and studies using Chk1 haploinsufficient mice initially suggested a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700047/ https://www.ncbi.nlm.nih.gov/pubmed/29167438 http://dx.doi.org/10.1038/s41467-017-01850-4 |
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author | Schuler, Fabian Weiss, Johannes G. Lindner, Silke E. Lohmüller, Michael Herzog, Sebastian Spiegl, Simon F. Menke, Philipp Geley, Stephan Labi, Verena Villunger, Andreas |
author_facet | Schuler, Fabian Weiss, Johannes G. Lindner, Silke E. Lohmüller, Michael Herzog, Sebastian Spiegl, Simon F. Menke, Philipp Geley, Stephan Labi, Verena Villunger, Andreas |
author_sort | Schuler, Fabian |
collection | PubMed |
description | Checkpoint kinase 1 (CHK1) is critical for intrinsic cell cycle control and coordination of cell cycle progression in response to DNA damage. Despite its essential function, CHK1 has been identified as a target to kill cancer cells and studies using Chk1 haploinsufficient mice initially suggested a role as tumor suppressor. Here, we report on the key role of CHK1 in normal B-cell development, lymphomagenesis and cell survival. Chemical CHK1 inhibition induces BCL2-regulated apoptosis in primary as well as malignant B-cells and CHK1 expression levels control the timing of lymphomagenesis in mice. Moreover, total ablation of Chk1 in B-cells arrests their development at the pro-B cell stage, a block that, surprisingly, cannot be overcome by inhibition of mitochondrial apoptosis, as cell cycle arrest is initiated as an alternative fate to limit the spread of damaged DNA. Our findings define CHK1 as essential in B-cell development and potent target to treat blood cancer. |
format | Online Article Text |
id | pubmed-5700047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57000472017-11-24 Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis Schuler, Fabian Weiss, Johannes G. Lindner, Silke E. Lohmüller, Michael Herzog, Sebastian Spiegl, Simon F. Menke, Philipp Geley, Stephan Labi, Verena Villunger, Andreas Nat Commun Article Checkpoint kinase 1 (CHK1) is critical for intrinsic cell cycle control and coordination of cell cycle progression in response to DNA damage. Despite its essential function, CHK1 has been identified as a target to kill cancer cells and studies using Chk1 haploinsufficient mice initially suggested a role as tumor suppressor. Here, we report on the key role of CHK1 in normal B-cell development, lymphomagenesis and cell survival. Chemical CHK1 inhibition induces BCL2-regulated apoptosis in primary as well as malignant B-cells and CHK1 expression levels control the timing of lymphomagenesis in mice. Moreover, total ablation of Chk1 in B-cells arrests their development at the pro-B cell stage, a block that, surprisingly, cannot be overcome by inhibition of mitochondrial apoptosis, as cell cycle arrest is initiated as an alternative fate to limit the spread of damaged DNA. Our findings define CHK1 as essential in B-cell development and potent target to treat blood cancer. Nature Publishing Group UK 2017-11-22 /pmc/articles/PMC5700047/ /pubmed/29167438 http://dx.doi.org/10.1038/s41467-017-01850-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schuler, Fabian Weiss, Johannes G. Lindner, Silke E. Lohmüller, Michael Herzog, Sebastian Spiegl, Simon F. Menke, Philipp Geley, Stephan Labi, Verena Villunger, Andreas Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis |
title | Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis |
title_full | Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis |
title_fullStr | Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis |
title_full_unstemmed | Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis |
title_short | Checkpoint kinase 1 is essential for normal B cell development and lymphomagenesis |
title_sort | checkpoint kinase 1 is essential for normal b cell development and lymphomagenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700047/ https://www.ncbi.nlm.nih.gov/pubmed/29167438 http://dx.doi.org/10.1038/s41467-017-01850-4 |
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