Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer
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Abstract
Methods
Patients with stages I to III breast cancer who were seen at a single cancer center between 2010 and 2012, and who agreed to participate in research DNA banking, were included (N = 488). Personal and family cancer histories were collected and germline DNA was sequenced with NGS to identify mutations.
Results
Deleterious mutations were identified in 10.7% of women, including 6.1% in BRCA1/2 (5.1% in non-Ashkenazi Jewish patients) and 4.6% in other breast/ovarian cancer predisposition genes including CHEK2 (n = 10), ATM (n = 4), BRIP1 (n = 4), and one each in PALB2, PTEN, NBN, RAD51C, RAD51D, MSH6, and PMS2. Whereas young age (P
Citation impact
556
total citations
- FWCI
- 48.88
- Percentile
- 100%
- References
- 56
Citations per year
Authors
9Topics & keywords
Topics
Keywords
- CHEK2
- PALB2
- Breast cancer
- MSH6
- Medicine
- Germline mutation
- Cancer
- Oncology
UN Sustainable Development Goals
- Good health and well-being
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