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DNA replication stress: a source of APOBEC3B expression in breast cancer
APOBEC cytidine deaminases have been implicated as major contributors to the mutation burden in many cancers on the basis of their mutational signature. A new experimental study sheds light on the inciting factors, linking APOBEC3B expression to oncogene- and drug-induced replication stress. ELECTRO...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045630/ https://www.ncbi.nlm.nih.gov/pubmed/27716362 http://dx.doi.org/10.1186/s13059-016-1069-y |
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author | Cescon, David W. Haibe-Kains, Benjamin |
author_facet | Cescon, David W. Haibe-Kains, Benjamin |
author_sort | Cescon, David W. |
collection | PubMed |
description | APOBEC cytidine deaminases have been implicated as major contributors to the mutation burden in many cancers on the basis of their mutational signature. A new experimental study sheds light on the inciting factors, linking APOBEC3B expression to oncogene- and drug-induced replication stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1069-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5045630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50456302016-10-05 DNA replication stress: a source of APOBEC3B expression in breast cancer Cescon, David W. Haibe-Kains, Benjamin Genome Biol Research Highlight APOBEC cytidine deaminases have been implicated as major contributors to the mutation burden in many cancers on the basis of their mutational signature. A new experimental study sheds light on the inciting factors, linking APOBEC3B expression to oncogene- and drug-induced replication stress. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1069-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-30 /pmc/articles/PMC5045630/ /pubmed/27716362 http://dx.doi.org/10.1186/s13059-016-1069-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Highlight Cescon, David W. Haibe-Kains, Benjamin DNA replication stress: a source of APOBEC3B expression in breast cancer |
title | DNA replication stress: a source of APOBEC3B expression in breast cancer |
title_full | DNA replication stress: a source of APOBEC3B expression in breast cancer |
title_fullStr | DNA replication stress: a source of APOBEC3B expression in breast cancer |
title_full_unstemmed | DNA replication stress: a source of APOBEC3B expression in breast cancer |
title_short | DNA replication stress: a source of APOBEC3B expression in breast cancer |
title_sort | dna replication stress: a source of apobec3b expression in breast cancer |
topic | Research Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5045630/ https://www.ncbi.nlm.nih.gov/pubmed/27716362 http://dx.doi.org/10.1186/s13059-016-1069-y |
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