학술논문

Germline mutations in CDH1 are infrequent in women with early-onset or familial lobular breast cancers
Document Type
article
Source
Journal of Medical Genetics. 48(1)
Subject
Biological Sciences
Biomedical and Clinical Sciences
Genetics
Oncology and Carcinogenesis
Clinical Research
Genetic Testing
Cancer
Breast Cancer
Human Genome
2.1 Biological and endogenous factors
Aetiology
Adult
Age of Onset
Antigens
CD
Breast Neoplasms
Cadherins
Carcinoma
Lobular
DNA Mutational Analysis
Family
Female
Germ-Line Mutation
Humans
Middle Aged
kConFab
Medical and Health Sciences
Genetics & Heredity
Clinical sciences
Language
Abstract
BackgroundGermline mutations in CDH1 are associated with hereditary diffuse gastric cancer; lobular breast cancer also occurs excessively in families with such condition.MethodTo determine if CDH1 is a susceptibility gene for lobular breast cancer in women without a family history of diffuse gastric cancer, germline DNA was analysed for the presence of CDH1 mutations in 318 women with lobular breast cancer who were diagnosed before the age of 45 years or had a family history of breast cancer and were not known, or known not, to be carriers of germline mutations in BRCA1 or BRCA2. Cases were ascertained through breast cancer registries and high-risk cancer genetic clinics (Breast Cancer Family Registry, the kConFab and a consortium of breast cancer genetics clinics in the United States and Spain). Additionally, Multiplex Ligation-dependent Probe Amplification was performed for 134 cases to detect large deletions.ResultsNo truncating mutations and no large deletions were detected. Six non-synonymous variants were found in seven families. Four (4/318 or 1.3%) are considered to be potentially pathogenic through in vitro and in silico analysis.ConclusionPotentially pathogenic germline CDH1 mutations in women with early-onset or familial lobular breast cancer are at most infrequent.