Hadjisavvas Andreas, Adamou Adamos, O'Dowd Phanis Catherine, Todd Christopher M, Kitsios Petros, Kyriacou Kyriacos, Christodoulou Christina G
Department of Electron Microscopy/Molecular Pathology, The Cyprus Institute of Neurology and Genetics, 1683 Nicosia, Cyprus.
Oncol Rep. 2002 Mar-Apr;9(2):383-6.
A molecular study was performed on BRCA1 and BRCA2 genes in a Cypriot family, with a history of both male and female breast cancers. Three variants were detected in the BRCA1 gene, two of which are missense mutations at nucleotide positions 1186 in exon 11 (Q356R), and 4654 in exon 15 (S1512I). The third variant is a polymorphism at position 2430 in exon 11 (771L). Similarly in the BRCA2 gene two variants were detected: a missense mutation at position 1342, exon 10 (H372N), and a polymorphism at position 3624 in exon 11 (1132K). Since these BRCA2 variants appear to be polymorphisms in the Cypriot population, we suggest that the two BRCA1 mutations, Q356R and S1512I, may be related to the breast cancer phenotype.
对一个有男性和女性乳腺癌病史的塞浦路斯家族的BRCA1和BRCA2基因进行了分子研究。在BRCA1基因中检测到三个变异,其中两个是外显子11中核苷酸位置1186处的错义突变(Q356R)和外显子15中核苷酸位置4654处的错义突变(S1512I)。第三个变异是外显子11中位置2430处的多态性(771L)。同样,在BRCA2基因中检测到两个变异:外显子10中位置1342处的错义突变(H372N)和外显子11中位置3624处的多态性(1132K)。由于这些BRCA2变异在塞浦路斯人群中似乎是多态性,我们认为两个BRCA1突变,Q356R和S1512I,可能与乳腺癌表型有关。