Cargando…
Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas
BRCA1 and BRCA2 mutations are responsible for hereditary breast and ovarian cancer, but they also confer an increased risk for the development of rarer cancers associated with this syndrome, namely, cancer of the pancreas, male breast, peritoneum, and fallopian tube. The objective of this work was t...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988637/ https://www.ncbi.nlm.nih.gov/pubmed/27532258 http://dx.doi.org/10.1371/journal.pone.0161438 |
_version_ | 1782448453594382336 |
---|---|
author | Pinto, Pedro Peixoto, Ana Santos, Catarina Rocha, Patrícia Pinto, Carla Pinheiro, Manuela Leça, Luís Martins, Ana Teresa Ferreira, Verónica Bartosch, Carla Teixeira, Manuel R. |
author_facet | Pinto, Pedro Peixoto, Ana Santos, Catarina Rocha, Patrícia Pinto, Carla Pinheiro, Manuela Leça, Luís Martins, Ana Teresa Ferreira, Verónica Bartosch, Carla Teixeira, Manuel R. |
author_sort | Pinto, Pedro |
collection | PubMed |
description | BRCA1 and BRCA2 mutations are responsible for hereditary breast and ovarian cancer, but they also confer an increased risk for the development of rarer cancers associated with this syndrome, namely, cancer of the pancreas, male breast, peritoneum, and fallopian tube. The objective of this work was to quantify the contribution of the founder mutations BRCA2 c.156_157insAlu and BRCA1 c.3331_3334del for cancer etiology in unselected hospital-based cohorts of Portuguese patients diagnosed with these rarer cancers, by using a strategy that included testing of archival tumor tissue. A total of 102 male breast, 68 pancreatic and 33 peritoneal/fallopian tube carcinoma cases were included in the study. The BRCA2 c.156_157insAlu mutation was observed with a frequency of 7.8% in male breast cancers, 3.0% in peritoneal/fallopian tube cancers, and 1.6% in pancreatic cancers, with estimated total contributions of germline BRCA2 mutations of 14.3%, 5.5%, and 2.8%, respectively. No carriers of the BRCA1 c.3331_3334del mutation were identified. During our study, a patient with an ampulla of Vater carcinoma was incidentally found to carry the BRCA2 c.156_157insAlu mutation, so we decided to test a consecutive series of additional 15 ampullary carcinomas for BRCA1/BRCA2 mutations using a combination of direct founder mutation testing and full gene analysis with next generation sequencing. BRCA2 mutations were observed with a frequency of 14.3% in ampulla of Vater carcinomas. In conclusion, taking into account the implications for both the individuals and their family members, we recommend that patients with these neoplasias should be offered BRCA1/BRCA2 genetic testing and we here show that it is feasible to test for founder mutations in archival tumor tissue. Furthermore, we identified for the first time a high frequency of germline BRCA2 mutations in ampullary cancers. |
format | Online Article Text |
id | pubmed-4988637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-49886372016-08-29 Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas Pinto, Pedro Peixoto, Ana Santos, Catarina Rocha, Patrícia Pinto, Carla Pinheiro, Manuela Leça, Luís Martins, Ana Teresa Ferreira, Verónica Bartosch, Carla Teixeira, Manuel R. PLoS One Research Article BRCA1 and BRCA2 mutations are responsible for hereditary breast and ovarian cancer, but they also confer an increased risk for the development of rarer cancers associated with this syndrome, namely, cancer of the pancreas, male breast, peritoneum, and fallopian tube. The objective of this work was to quantify the contribution of the founder mutations BRCA2 c.156_157insAlu and BRCA1 c.3331_3334del for cancer etiology in unselected hospital-based cohorts of Portuguese patients diagnosed with these rarer cancers, by using a strategy that included testing of archival tumor tissue. A total of 102 male breast, 68 pancreatic and 33 peritoneal/fallopian tube carcinoma cases were included in the study. The BRCA2 c.156_157insAlu mutation was observed with a frequency of 7.8% in male breast cancers, 3.0% in peritoneal/fallopian tube cancers, and 1.6% in pancreatic cancers, with estimated total contributions of germline BRCA2 mutations of 14.3%, 5.5%, and 2.8%, respectively. No carriers of the BRCA1 c.3331_3334del mutation were identified. During our study, a patient with an ampulla of Vater carcinoma was incidentally found to carry the BRCA2 c.156_157insAlu mutation, so we decided to test a consecutive series of additional 15 ampullary carcinomas for BRCA1/BRCA2 mutations using a combination of direct founder mutation testing and full gene analysis with next generation sequencing. BRCA2 mutations were observed with a frequency of 14.3% in ampulla of Vater carcinomas. In conclusion, taking into account the implications for both the individuals and their family members, we recommend that patients with these neoplasias should be offered BRCA1/BRCA2 genetic testing and we here show that it is feasible to test for founder mutations in archival tumor tissue. Furthermore, we identified for the first time a high frequency of germline BRCA2 mutations in ampullary cancers. Public Library of Science 2016-08-17 /pmc/articles/PMC4988637/ /pubmed/27532258 http://dx.doi.org/10.1371/journal.pone.0161438 Text en © 2016 Pinto et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Pinto, Pedro Peixoto, Ana Santos, Catarina Rocha, Patrícia Pinto, Carla Pinheiro, Manuela Leça, Luís Martins, Ana Teresa Ferreira, Verónica Bartosch, Carla Teixeira, Manuel R. Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas |
title | Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas |
title_full | Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas |
title_fullStr | Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas |
title_full_unstemmed | Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas |
title_short | Analysis of Founder Mutations in Rare Tumors Associated With Hereditary Breast/Ovarian Cancer Reveals a Novel Association of BRCA2 Mutations with Ampulla of Vater Carcinomas |
title_sort | analysis of founder mutations in rare tumors associated with hereditary breast/ovarian cancer reveals a novel association of brca2 mutations with ampulla of vater carcinomas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988637/ https://www.ncbi.nlm.nih.gov/pubmed/27532258 http://dx.doi.org/10.1371/journal.pone.0161438 |
work_keys_str_mv | AT pintopedro analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT peixotoana analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT santoscatarina analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT rochapatricia analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT pintocarla analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT pinheiromanuela analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT lecaluis analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT martinsanateresa analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT ferreiraveronica analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT bartoschcarla analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas AT teixeiramanuelr analysisoffoundermutationsinraretumorsassociatedwithhereditarybreastovariancancerrevealsanovelassociationofbrca2mutationswithampullaofvatercarcinomas |