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Germline MUTYH gene mutations are not frequently found in unselected patients with papillary breast carcinoma.

Authors :
Boesaard EP
Vogelaar IP
Bult P
Wauters CA
van Krieken JH
Ligtenberg MJ
van der Post RS
Hoogerbrugge N
Source :
Hereditary cancer in clinical practice [Hered Cancer Clin Pract] 2014 Dec 12; Vol. 12 (1), pp. 21. Date of Electronic Publication: 2014 Dec 12 (Print Publication: 2014).
Publication Year :
2014

Abstract

MUTYH-associated polyposis (MAP) is an autosomal recessive disease, which predisposes to polyposis and colorectal cancer. There is a trend towards an increased risk of breast cancer in MAP patients, with a remarkable proportion of papillary breast cancers. To determine whether MUTYH mutations are associated with this specific and rare type of breast cancer, 53 unselected patients with papillary breast cancer were analyzed for founder mutations in the MUTYH gene. No germline mutations were identified, indicating that biallelic MUTYH mutations are not a frequent underlying cause for the development of papillary carcinomas of the breast.

Details

Language :
English
ISSN :
1731-2302
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Hereditary cancer in clinical practice
Publication Type :
Academic Journal
Accession number :
25937855
Full Text :
https://doi.org/10.1186/1897-4287-12-21