Please use this identifier to cite or link to this item: https://repositorio.ufrn.br/handle/123456789/27644
Title: Influence of BRCA1 germline mutations in the somatic mutational burden of triple-negative breast cancer
Authors: Ferreira, Elisa Napolitano
Brianese, Rafael Canfield
Almeida, Renan Valieris Bueno de
Drummond, Rodrigo Duarte
Souza, Jorge Estefano de
Silva, Israel Tojal da
Souza, Sandro José de
Carraro, Dirce Maria
Keywords: Breast neoplasms;triple negative breast neoplasms;BRCA1
Issue Date: Aug-2019
Citation: FERREIRA, E. N.; BRIANESE, R. C.; ALMEIDA, R. V. B.; DRUMMOND, R. D.; SOUZA, J. E.; SILVA, I. T.; SOUZA, S. J.; CARRARO, D. M. Influence of BRCA1 germline mutations in the somatic mutational burden of triple-negative breast cancer. Transl Oncol., [s. l.], v. 12, n. 11, p. 1453-1460, ago. 2019. DOI: 10.1016/j.tranon.2019.07.016. Disponível em: https://www.sciencedirect.com/science/article/pii/S1936523319302232?via%3Dihub. Acesso em: 05 set. 2019.
Portuguese Abstract: The majority of the hereditary triple-negative breast cancers (TNBCs) are associated with BRCA1 germline mutations. Nevertheless, the understanding of the role of BRCA1 deficiency in the TNBC tumorigenesis is poor. In this sense, we performed whole-exome sequencing of triplet samples (leucocyte, tumor, and normal-adjacent breast tissue) for 10 cases of early-onset TNBC, including 5 hereditary (with BRCA1 germline pathogenic mutation) and 5 sporadic (with no BRCA1 or BRCA2 germline pathogenic mutations), for assessing the somatic mutation repertoire. Protein-affecting somatic mutations were identified for both mammary tissues, and Ingenuity Pathway Analysis was used to investigate gene interactions. BRCA1 and RAD51C somatic promoter methylation in tumor samples was also investigated by bisulfite sequencing. Sporadic tumors had higher proportion of driver mutations (≥25% allele frequency) than BRCA1 hereditary tumors, whereas no difference was detected in the normal breast samples. Distinct gene networks were obtained from the driver genes in each group. The Cancer Genome Atlas data analysis of TNBC classified as hereditary and sporadic reinforced our findings. The data presented here indicate that in the absence of BRCA1 germline mutations, a higher number of driver mutations are required for tumor development and that different defective processes are operating in the tumorigenesis of hereditary and sporadic TNBC in young women.
URI: https://repositorio.ufrn.br/jspui/handle/123456789/27644
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