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Current perspectives on CHEK2 mutations in breast cancer
Checkpoint kinase 2 (CHEK2) is a serine/threonine kinase which is activated upon DNA damage and is implicated in pathways that govern DNA repair, cell cycle arrest or apoptosis in response to the initial damage. Loss of kinase function has been correlated with different types of cancer, mainly breas...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439543/ https://www.ncbi.nlm.nih.gov/pubmed/28553140 http://dx.doi.org/10.2147/BCTT.S111394 |
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author | Apostolou, Panagiotis Papasotiriou, Ioannis |
author_facet | Apostolou, Panagiotis Papasotiriou, Ioannis |
author_sort | Apostolou, Panagiotis |
collection | PubMed |
description | Checkpoint kinase 2 (CHEK2) is a serine/threonine kinase which is activated upon DNA damage and is implicated in pathways that govern DNA repair, cell cycle arrest or apoptosis in response to the initial damage. Loss of kinase function has been correlated with different types of cancer, mainly breast cancer. CHEK2 functionality is affected by different missense or deleterious mutations. CHEK2*1100delC and I157T are most studied in populations all over the world. Although these variants have been identified in patients with breast cancer, their frequency raises doubts about their importance as risk factors. The present article reviews the recent advances in research on CHEK2 mutations, focusing on breast cancer, based on the latest experimental data. |
format | Online Article Text |
id | pubmed-5439543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54395432017-05-26 Current perspectives on CHEK2 mutations in breast cancer Apostolou, Panagiotis Papasotiriou, Ioannis Breast Cancer (Dove Med Press) Review Checkpoint kinase 2 (CHEK2) is a serine/threonine kinase which is activated upon DNA damage and is implicated in pathways that govern DNA repair, cell cycle arrest or apoptosis in response to the initial damage. Loss of kinase function has been correlated with different types of cancer, mainly breast cancer. CHEK2 functionality is affected by different missense or deleterious mutations. CHEK2*1100delC and I157T are most studied in populations all over the world. Although these variants have been identified in patients with breast cancer, their frequency raises doubts about their importance as risk factors. The present article reviews the recent advances in research on CHEK2 mutations, focusing on breast cancer, based on the latest experimental data. Dove Medical Press 2017-05-12 /pmc/articles/PMC5439543/ /pubmed/28553140 http://dx.doi.org/10.2147/BCTT.S111394 Text en © 2017 Apostolou and Papasotiriou. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Apostolou, Panagiotis Papasotiriou, Ioannis Current perspectives on CHEK2 mutations in breast cancer |
title | Current perspectives on CHEK2 mutations in breast cancer |
title_full | Current perspectives on CHEK2 mutations in breast cancer |
title_fullStr | Current perspectives on CHEK2 mutations in breast cancer |
title_full_unstemmed | Current perspectives on CHEK2 mutations in breast cancer |
title_short | Current perspectives on CHEK2 mutations in breast cancer |
title_sort | current perspectives on chek2 mutations in breast cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5439543/ https://www.ncbi.nlm.nih.gov/pubmed/28553140 http://dx.doi.org/10.2147/BCTT.S111394 |
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