Research and Development Division, Genoprimer Diagnóstico Molecular, Curitiba, Paraná, Brazil.
Molecular Biology Clinical Laboratory, Clinimol Diagnóstico Molecular, São Paulo, São Paulo, Brazil.
Mol Genet Genomic Med. 2024 Aug;12(8):e2504. doi: 10.1002/mgg3.2504.
In this article, we delineate a loosely selected cohort comprising patients with a history of early-onset breast cancer and/or a familial occurrence of cancer. The aim of this study was to gain insights into the presence of breast cancer-related gene variants in a population from a micro-region in southern Brazil, specifically the Metropolitan Region of Curitiba. This area exhibits a highly genetically mixed population, mirroring the general characteristics of the Brazilian people.
Comprehensive next-generation sequencing (NGS) multigene panel testing was conducted on 12 patients from the region, utilizing three different library preparation methods.
Two pathogenic variants and one candidate pathogenic variant were identified: BRCA2 c.8878C>T, p.Gln2960Ter; CHEK2 c.1100del, p.Thr367Metfs15, and BRCA2 c.3482dup, p.Asp1161Glufs3.
BRCA2 c.3482dup, a novel candidate pathogenic variant, previously unpublished, is reported. The prevalence of pathogenic variants in this small cohort is similar to that described in the literature. All different library preparation methods were equally proficient in enabling the detection of these variants.
在本文中,我们描述了一个由具有早发性乳腺癌病史和/或家族性癌症史的患者组成的松散选择队列。本研究的目的是深入了解巴西南部一个微地区,即库里蒂巴大都市区人群中乳腺癌相关基因变异的存在情况。该地区的人口具有高度混合的遗传特征,反映了巴西人民的一般特征。
对来自该地区的 12 名患者进行了综合下一代测序(NGS)多基因panel 检测,使用了三种不同的文库制备方法。
发现了两个致病性变异和一个候选致病性变异:BRCA2 c.8878C>T,p.Gln2960Ter;CHEK2 c.1100del,p.Thr367Metfs15 和 BRCA2 c.3482dup,p.Asp1161Glufs3。
报告了一种以前未发表的新的候选致病性变异 BRCA2 c.3482dup。这个小队列中的致病性变异的患病率与文献中描述的相似。所有不同的文库制备方法在检测这些变异方面同样有效。