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Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations
Breast cancer diagnosed during pregnancy (BCP) is a rare and highly challenging disease. To investigate the impact of pregnancy on the biology of breast cancer, we conducted a comparative analysis of a cohort of BCP patients and non-pregnant control patients by integrating gene expression, copy numb...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078984/ https://www.ncbi.nlm.nih.gov/pubmed/30109263 http://dx.doi.org/10.1038/s41523-018-0077-3 |
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author | Nguyen, Bastien Venet, David Azim, Hatem A. Brown, David Desmedt, Christine Lambertini, Matteo Majjaj, Samira Pruneri, Giancarlo Peccatori, Fedro Piccart, Martine Rothé, Françoise Sotiriou, Christos |
author_facet | Nguyen, Bastien Venet, David Azim, Hatem A. Brown, David Desmedt, Christine Lambertini, Matteo Majjaj, Samira Pruneri, Giancarlo Peccatori, Fedro Piccart, Martine Rothé, Françoise Sotiriou, Christos |
author_sort | Nguyen, Bastien |
collection | PubMed |
description | Breast cancer diagnosed during pregnancy (BCP) is a rare and highly challenging disease. To investigate the impact of pregnancy on the biology of breast cancer, we conducted a comparative analysis of a cohort of BCP patients and non-pregnant control patients by integrating gene expression, copy number alterations and whole genome sequencing data. We showed that BCP exhibit unique molecular characteristics including an enrichment of non-silent mutations, a higher frequency of mutations in mucin gene family and an enrichment of mismatch repair deficiency mutational signature. This provides important insights into the biology of BCP and suggests that these features may be implicated in promoting tumor progression during pregnancy. In addition, it provides an unprecedented resource for further understanding the biology of breast cancer in young women and how pregnancy could modulate tumor biology. |
format | Online Article Text |
id | pubmed-6078984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60789842018-08-14 Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations Nguyen, Bastien Venet, David Azim, Hatem A. Brown, David Desmedt, Christine Lambertini, Matteo Majjaj, Samira Pruneri, Giancarlo Peccatori, Fedro Piccart, Martine Rothé, Françoise Sotiriou, Christos NPJ Breast Cancer Article Breast cancer diagnosed during pregnancy (BCP) is a rare and highly challenging disease. To investigate the impact of pregnancy on the biology of breast cancer, we conducted a comparative analysis of a cohort of BCP patients and non-pregnant control patients by integrating gene expression, copy number alterations and whole genome sequencing data. We showed that BCP exhibit unique molecular characteristics including an enrichment of non-silent mutations, a higher frequency of mutations in mucin gene family and an enrichment of mismatch repair deficiency mutational signature. This provides important insights into the biology of BCP and suggests that these features may be implicated in promoting tumor progression during pregnancy. In addition, it provides an unprecedented resource for further understanding the biology of breast cancer in young women and how pregnancy could modulate tumor biology. Nature Publishing Group UK 2018-08-06 /pmc/articles/PMC6078984/ /pubmed/30109263 http://dx.doi.org/10.1038/s41523-018-0077-3 Text en © The Author(s) 2018 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 Nguyen, Bastien Venet, David Azim, Hatem A. Brown, David Desmedt, Christine Lambertini, Matteo Majjaj, Samira Pruneri, Giancarlo Peccatori, Fedro Piccart, Martine Rothé, Françoise Sotiriou, Christos Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations |
title | Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations |
title_full | Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations |
title_fullStr | Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations |
title_full_unstemmed | Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations |
title_short | Breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations |
title_sort | breast cancer diagnosed during pregnancy is associated with enrichment of non-silent mutations, mismatch repair deficiency signature and mucin mutations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078984/ https://www.ncbi.nlm.nih.gov/pubmed/30109263 http://dx.doi.org/10.1038/s41523-018-0077-3 |
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