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Germline and Somatic mutations in postmenopausal breast cancer patients

OBJECTIVES: In breast cancer (BC) patients, the frequency of germline BRCA mutations (gBRCA) may vary according to the ethnic background, age, and family history of cancer. Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) is the second most common somatic mutated gene...

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Autores principales: Nagy, Tauana Rodrigues, Maistro, Simone, Encinas, Giselly, Katayama, Maria Lucia Hirata, Pereira, Glaucia Fernanda de Lima, Gaburo-Júnior, Nelson, Franco, Lucas Augusto Moyses, de Gouvêa, Ana Carolina Ribeiro Chaves, Diz, Maria del Pilar Estevez, Leite, Luiz Antonio Senna, Folgueira, Maria Aparecida Azevedo Koike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculdade de Medicina / USP 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266163/
https://www.ncbi.nlm.nih.gov/pubmed/34287479
http://dx.doi.org/10.6061/clinics/2021/e2837
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author Nagy, Tauana Rodrigues
Maistro, Simone
Encinas, Giselly
Katayama, Maria Lucia Hirata
Pereira, Glaucia Fernanda de Lima
Gaburo-Júnior, Nelson
Franco, Lucas Augusto Moyses
de Gouvêa, Ana Carolina Ribeiro Chaves
Diz, Maria del Pilar Estevez
Leite, Luiz Antonio Senna
Folgueira, Maria Aparecida Azevedo Koike
author_facet Nagy, Tauana Rodrigues
Maistro, Simone
Encinas, Giselly
Katayama, Maria Lucia Hirata
Pereira, Glaucia Fernanda de Lima
Gaburo-Júnior, Nelson
Franco, Lucas Augusto Moyses
de Gouvêa, Ana Carolina Ribeiro Chaves
Diz, Maria del Pilar Estevez
Leite, Luiz Antonio Senna
Folgueira, Maria Aparecida Azevedo Koike
author_sort Nagy, Tauana Rodrigues
collection PubMed
description OBJECTIVES: In breast cancer (BC) patients, the frequency of germline BRCA mutations (gBRCA) may vary according to the ethnic background, age, and family history of cancer. Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) is the second most common somatic mutated gene in BC; however, the association of mutations in both genes with cancer has not been thoroughly investigated. Thus, our aims were to investigate gBRCA mutation frequency in a cohort of postmenopausal Brazilian BC patients and the association of gBRCA1/BRCA2 and PIK3CA somatic mutations. METHODS: Forty-nine postmenopausal (>55 years) and forty-one young (≤35 years) BC patients were included in this study. The postmenopausal group included patients who reported a positive family history of cancer. For these patients, gBRCA1/BRCA2 were sequenced using next-generation sequencing (NGS) or Sanger sequencing. Data for gBRCA in young patients were already available from a previous study. DNA from formalin-fixed, paraffin-embedded (FFPE) tumors was obtained from 27 postmenopausal and 41 young patients for analyzing exons 9 and 20 of PIK3CA. The association between gBRCA1/BRCA2 and somatic mutations in PIK3CA was investigated. RESULTS: The overall frequency of gBRCA1/BRCA2 among the 49 postmenopausal patients was 10.2%. The frequencies of somatic mutations in PIK3CA in the postmenopausal and young patients were 37% and 17%, respectively (ns). The most common PIK3CA mutation was found to be E454A. Nonsense and frameshift mutations, which may counteract the oncogenic potential of PIK3CA were also detected. Regardless of age, 25% of BRCA1/BRCA2 mutation carriers and non-carriers , each, had PIK3CA somatic mutations. CONCLUSIONS: Data obtained indicate that BRCA1/BRCA2 gene testing may be considered for postmenopausal patients with BC who have a family history of cancer. Although some of them are not considered pathogenic, somatic variants of PIK3CA are frequently observed in BC patients, especially in postmenopausal patients.
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spelling pubmed-82661632021-07-09 Germline and Somatic mutations in postmenopausal breast cancer patients Nagy, Tauana Rodrigues Maistro, Simone Encinas, Giselly Katayama, Maria Lucia Hirata Pereira, Glaucia Fernanda de Lima Gaburo-Júnior, Nelson Franco, Lucas Augusto Moyses de Gouvêa, Ana Carolina Ribeiro Chaves Diz, Maria del Pilar Estevez Leite, Luiz Antonio Senna Folgueira, Maria Aparecida Azevedo Koike Clinics (Sao Paulo) Original Article OBJECTIVES: In breast cancer (BC) patients, the frequency of germline BRCA mutations (gBRCA) may vary according to the ethnic background, age, and family history of cancer. Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) is the second most common somatic mutated gene in BC; however, the association of mutations in both genes with cancer has not been thoroughly investigated. Thus, our aims were to investigate gBRCA mutation frequency in a cohort of postmenopausal Brazilian BC patients and the association of gBRCA1/BRCA2 and PIK3CA somatic mutations. METHODS: Forty-nine postmenopausal (>55 years) and forty-one young (≤35 years) BC patients were included in this study. The postmenopausal group included patients who reported a positive family history of cancer. For these patients, gBRCA1/BRCA2 were sequenced using next-generation sequencing (NGS) or Sanger sequencing. Data for gBRCA in young patients were already available from a previous study. DNA from formalin-fixed, paraffin-embedded (FFPE) tumors was obtained from 27 postmenopausal and 41 young patients for analyzing exons 9 and 20 of PIK3CA. The association between gBRCA1/BRCA2 and somatic mutations in PIK3CA was investigated. RESULTS: The overall frequency of gBRCA1/BRCA2 among the 49 postmenopausal patients was 10.2%. The frequencies of somatic mutations in PIK3CA in the postmenopausal and young patients were 37% and 17%, respectively (ns). The most common PIK3CA mutation was found to be E454A. Nonsense and frameshift mutations, which may counteract the oncogenic potential of PIK3CA were also detected. Regardless of age, 25% of BRCA1/BRCA2 mutation carriers and non-carriers , each, had PIK3CA somatic mutations. CONCLUSIONS: Data obtained indicate that BRCA1/BRCA2 gene testing may be considered for postmenopausal patients with BC who have a family history of cancer. Although some of them are not considered pathogenic, somatic variants of PIK3CA are frequently observed in BC patients, especially in postmenopausal patients. Faculdade de Medicina / USP 2021-07-08 2021 /pmc/articles/PMC8266163/ /pubmed/34287479 http://dx.doi.org/10.6061/clinics/2021/e2837 Text en Copyright © 2021 CLINICS https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited.
spellingShingle Original Article
Nagy, Tauana Rodrigues
Maistro, Simone
Encinas, Giselly
Katayama, Maria Lucia Hirata
Pereira, Glaucia Fernanda de Lima
Gaburo-Júnior, Nelson
Franco, Lucas Augusto Moyses
de Gouvêa, Ana Carolina Ribeiro Chaves
Diz, Maria del Pilar Estevez
Leite, Luiz Antonio Senna
Folgueira, Maria Aparecida Azevedo Koike
Germline and Somatic mutations in postmenopausal breast cancer patients
title Germline and Somatic mutations in postmenopausal breast cancer patients
title_full Germline and Somatic mutations in postmenopausal breast cancer patients
title_fullStr Germline and Somatic mutations in postmenopausal breast cancer patients
title_full_unstemmed Germline and Somatic mutations in postmenopausal breast cancer patients
title_short Germline and Somatic mutations in postmenopausal breast cancer patients
title_sort germline and somatic mutations in postmenopausal breast cancer patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266163/
https://www.ncbi.nlm.nih.gov/pubmed/34287479
http://dx.doi.org/10.6061/clinics/2021/e2837
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