Low frequency of BRCA1 germline mutations in 45 German breast/ovarian cancer families.
Open Access
- 1 November 1997
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 34 (11) , 884-888
- https://doi.org/10.1136/jmg.34.11.884
Abstract
In this study we investigated 45 German breast/ovarian cancer families for germline mutations in the BRCA1 gene. We identified four germline mutations in three breast cancer families and in one breast-ovarian cancer family. among these were one frameshift mutation, one nonsense mutation, one novel splice site mutation, and one missense mutation. The missense mutation was also found in 2.8% of the general population, suggesting that it is not disease associated. The average age of disease onset in those families harbouring causative mutations was between 32.3 and 37.4 years, whereas the family harbouring the missense mutation had an average age of onset of 51.2 years. These findings show that BRCA1 is implicated in a small fraction of breast/ovarian cancer families suggesting the involvement of another susceptibility gene(s).Keywords
This publication has 31 references indexed in Scilit:
- Identification of a RING protein that can interact in vivo with the BRCA1 gene productNature Genetics, 1996
- Human, canine and murine BRCA1 genes: sequence comparison among speciesHuman Molecular Genetics, 1996
- German family study on hereditary breast-ovarian cancer.Journal of Medical Genetics, 1996
- Expression of Brca1 is associated with terminal differentiation of ectodermally and mesodermally derived tissues in mice.Genes & Development, 1995
- Detection of BRCA1 mutations by the protein truncation testHuman Molecular Genetics, 1995
- The developmental pattern of Brca1 expression implies a role in differentiation of the breast and other tissuesNature Genetics, 1995
- High allele loss rates at I7q I2‐q2I in breast and ovarian tumors from BRCAI‐linked familiesGenes, Chromosomes and Cancer, 1995
- Risks of cancer in BRCA1-mutation carriersThe Lancet, 1994
- Allele losses in the region 17q12–21 in familial breast and ovarian cancer involve the wild–type chromosomeNature Genetics, 1992
- Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21Science, 1990