Genetic testing · 2000
The founder mutations in the BRCA1, BRCA2, and ATM genes in Moroccan Jewish women with breast cancer.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Kreiss Y, Barak F, Baruch R G, Levy-Lahad E, Pras E, Friedman E
Аннотация
To gain insight into the molecular mechanisms underlying the inherited predisposition to breast cancer in non-Ashkenazi Jews, we genotyped 54 Jewish Moroccan women with breast cancer, unselected for family history of cancer, for the predominant Jewish mutations in BRCA1, BRCA2, and ATM. One patient (2%) was found to have the 185de1AG BRCA1 mutation, none was a carrier of the 6174delT BRCA2 mutation, and 2/54 (4%) were heterozygous for the ATM mutation. These rates were not significantly different from the rates in the general non-Ashkenazi population. These preliminary data may indicate that the predominant Jewish mutations in BRCA1, BRCA2, and ATM genes contribute little, if any, to breast cancer predisposition and risk among Moroccan Jews.
Предметные рубрики MeSH
AdultAgedAtaxia Telangiectasia Mutated ProteinsBRCA2 ProteinBreast NeoplasmsCell Cycle ProteinsDNA-Binding ProteinsFemaleFounder EffectGene FrequencyGenes, BRCA1Genetic Predisposition to DiseaseGenotypeHumansJewsMiddle AgedMoroccoMutationNeoplasm ProteinsPolymerase Chain ReactionProtein Serine-Threonine KinasesSequence DeletionTranscription FactorsTumor Suppressor Proteins