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Germline mutations in BRCA1, BRCA2, CHEK2 and TP53 in patients at high-risk for HBOC: characterizing a Northeast Brazilian Population

2014; Springer Nature; Volume: 1; Issue: 1 Linguagem: Inglês

10.1038/hgv.2014.12

2054-345X

Gabriela Trindade Felix, Camila Abe-Sandes, Taísa MB Machado-Lopes, Thaís Ferreira Bomfim, Rodrigo Santa Cruz Guindalini, Vanessa Catarine SAR Santos, Lorena Meyer, Polyanna Carôzo de Oliveira, João Cláudio Neiva, Roberto Meyer, Maura Romeo, Maria Betânia Pereira Toralles, Ivana Nascimento, Kiyoko Abe‐Sandes,

Genetic factors in colorectal cancer

Considering the importance of BRCA1, BRCA2, CHEK2 and TP53 in the development of hereditary early-onset breast and ovarian cancer and that the genetic susceptibility profile of the Northeast population from Brazil has never been analyzed, this study aimed to verify the frequency of mutations of clinical significance in these genes in high-risk hereditary breast and ovarian cancer (HBOC) syndrome patients from that region. DNA samples from 106 high-risk unrelated patients mostly from Bahia, the biggest state in the Northeast region, were analyzed. These patients underwent full BRCA1 gene sequencing, screening for common founder mutations in the BRCA2, CHEK2 and TP53 genes and genetic ancestry analysis with nine ancestry informative markers. The positive results were confirmed by two sequencing reactions. Three mutations of clinical significance were found: BRCA1 p.R71G (4.71%), 3450del4 (3.77%) and TP53 p.R337H (0.94%). The genetic ancestry analysis showed a high European ancestry contribution (62.2%) as well as considerable African (31.2%) and Amerindian (6.6%) ancestry contributions (r2=0.991); this degree of heterogeneity was also significant in the population structure analysis (r=0.604). This population is highly admixed with a different spectrum of genetic susceptibility, with the Galician founder mutation BRCA1 p.R71G accounting for 50% of all identified mutations in high-risk HBOC patients. TP53 p.R337H was also significantly frequent; thus, the combined screening of BRCA1/2 and TP53 should be offered to high-risk HBOC patients from Northeast Brazil. Gene sequencing of Bahian Brazilians at high risk for breast and ovarian cancer reveals that they should routinely be offered screening. The genes BRCA1, BRCA2 and TP53 are often mutated in families with a history of breast and ovarian cancer but the extent to which variation in these genes affected predisposition for these cancers in Brazilians from the north-eastern state of Bahia was unclear. A research group led by Ivana Nascimento and Kiyoko Abe-Sandes at the Universidade Federal da Bahia in Salvador, Brazil, sequenced these genes in 106 Bahian patients with a family history of breast and ovarian cancer. They found variants in those genes that had previously been linked to cancer in other populations, suggesting that screening for these genes should be routine in Bahian Brazilians with a family history of disease.