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CHK2 kinase in the DNA damage response and beyond

The serine/threonine kinase CHK2 is a key component of the DNA damage response. In human cells, following genotoxic stress, CHK2 is activated and phosphorylates >20 proteins to induce the appropriate cellular response, which, depending on the extent of damage, the cell type, and other factors, co...

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Detalles Bibliográficos
Autores principales: Zannini, Laura, Delia, Domenico, Buscemi, Giacomo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296918/
https://www.ncbi.nlm.nih.gov/pubmed/25404613
http://dx.doi.org/10.1093/jmcb/mju045
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author Zannini, Laura
Delia, Domenico
Buscemi, Giacomo
author_facet Zannini, Laura
Delia, Domenico
Buscemi, Giacomo
author_sort Zannini, Laura
collection PubMed
description The serine/threonine kinase CHK2 is a key component of the DNA damage response. In human cells, following genotoxic stress, CHK2 is activated and phosphorylates >20 proteins to induce the appropriate cellular response, which, depending on the extent of damage, the cell type, and other factors, could be cell cycle checkpoint activation, induction of apoptosis or senescence, DNA repair, or tolerance of the damage. Recently, CHK2 has also been found to have cellular functions independent of the presence of nuclear DNA lesions. In particular, CHK2 participates in several molecular processes involved in DNA structure modification and cell cycle progression. In this review, we discuss the activity of CHK2 in response to DNA damage and in the maintenance of the biological functions in unstressed cells. These activities are also considered in relation to a possible role of CHK2 in tumorigenesis and, as a consequence, as a target of cancer therapy.
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spelling pubmed-42969182015-02-02 CHK2 kinase in the DNA damage response and beyond Zannini, Laura Delia, Domenico Buscemi, Giacomo J Mol Cell Biol Review The serine/threonine kinase CHK2 is a key component of the DNA damage response. In human cells, following genotoxic stress, CHK2 is activated and phosphorylates >20 proteins to induce the appropriate cellular response, which, depending on the extent of damage, the cell type, and other factors, could be cell cycle checkpoint activation, induction of apoptosis or senescence, DNA repair, or tolerance of the damage. Recently, CHK2 has also been found to have cellular functions independent of the presence of nuclear DNA lesions. In particular, CHK2 participates in several molecular processes involved in DNA structure modification and cell cycle progression. In this review, we discuss the activity of CHK2 in response to DNA damage and in the maintenance of the biological functions in unstressed cells. These activities are also considered in relation to a possible role of CHK2 in tumorigenesis and, as a consequence, as a target of cancer therapy. Oxford University Press 2014-12 2014-11-17 /pmc/articles/PMC4296918/ /pubmed/25404613 http://dx.doi.org/10.1093/jmcb/mju045 Text en © The Author (2014). Published by Oxford University Press on behalf of Journal of Molecular Cell Biology, IBCB, SIBS, CAS. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Zannini, Laura
Delia, Domenico
Buscemi, Giacomo
CHK2 kinase in the DNA damage response and beyond
title CHK2 kinase in the DNA damage response and beyond
title_full CHK2 kinase in the DNA damage response and beyond
title_fullStr CHK2 kinase in the DNA damage response and beyond
title_full_unstemmed CHK2 kinase in the DNA damage response and beyond
title_short CHK2 kinase in the DNA damage response and beyond
title_sort chk2 kinase in the dna damage response and beyond
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296918/
https://www.ncbi.nlm.nih.gov/pubmed/25404613
http://dx.doi.org/10.1093/jmcb/mju045
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