BRCA1/2 mutation spectrum in armenian patients with breast and ovarian cancers
Автор: Belysheva Y.V., Bakaeva E.K., Venina A.R., Romanko A.A., Raskin G.A., Sokolenko A.P., Suspitsin E.N., Avetisyan A.A., Orlov S.V., Imyanitov E.N.
Журнал: Сибирский онкологический журнал @siboncoj
Рубрика: Лабораторные и экспериментальные исследования
Статья в выпуске: 6 т.22, 2023 года.
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The aim of the study was to compare the spectra of pathogenic BRCA1 and BRCA2 variants in patients with hereditary breast cancer (BC) and ovarian cancer (OC) from two groups of ethnic Armenians: Yerevan and cities of southern Russia. Material and Methods. 106 BC patients from the V.A. Fanardjian National Centre of Oncology (Yerevan, Republic of Armenia) and 117 BC and OC patients of Armenian origin who were referred to the Petrov National Medical Centre of Oncology (St. Petersburg, Russia) from several cancer centers of Russia (Krasnodar, Sochi, Pyatigorsk) were included into the study. The coding sequences of BRCA1 and BRCA2 genes were analyzed by the method of targeted high-throughput sequencing.
Breast cancer, ovarian cancer, hereditary cancer syndrome, founder effect, molecular genetics, molecular oncology
Короткий адрес: https://sciup.org/140303563
IDR: 140303563 | DOI: 10.21294/1814-4861-2023-22-6-83-91