Clinical Genetics · 2011 · 29 citations · 25 references
Life SciencesGeneticsOncologyCancer GeneticsMedical GeneticsMolecular OncologyCancer GenomicsHereditary Cancer SyndromesMutation AnalysisOncogene MutationsVariant DetectionBlood Sample CollectionBrca MutationsBreast Cancer HistoryDna ExtractionFamilial Breast CancerFamilial Cancer RiskGastric Cancer Prevalence
The contribution of mutations in BRCA1 and BRCA2 genes to the burden of breast cancer in Costa Rica has not been studied. We estimated the frequency of BRCA mutations among 111 Costa Rican women with breast cancer and a family history of breast cancer. These women were mainly from the metropolitan area of San José. A detailed family history was obtained from each patient and a blood sample was processed for DNA extraction. Mutations in BRCA1 and BRCA2 were sought using a combination of techniques and all mutations were confirmed by direct sequencing. Four different mutations were identified in five patients (four in BRCA2 and one in BRCA1) representing 4.5% of the total. Two unrelated patients were found to have a BRCA2 5531delTT mutation. Other BRCA2 mutations included C5507G and 6174delT. Only one BRCA1 mutation was found (C3522T). The family with the BRCA1 mutation had five cases of gastric cancer. Families with BRCA2 mutations were also reported to have cases of gastric and prostate cancers; however, the full range of cancers associated with BRCA1 and BRCA2 mutations in Costa Rica has not yet been established.
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Risks of cancer in BRCA1-mutation carriers
Daniel Ford · The Lancet · 1994 · 1.9K citations
Life Sciences, Genetics, Oncology +12
Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer
Tom Walsh, Silvia Casadei, Kathryn Hale Coats et al. · JAMA · 2006 · 666 citations