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PMID: 20816575 Published · ppublish English

Breast cancer predisposition syndromes.

Hematology/oncology clinics of North America ·Vol. 24 ·No. 5 ·2011-01-21

Hemel Deborah, Domchek Susan M

Abstract

A small, but important, percentage of breast cancer cases is caused by the inheritance of a single copy of a mutated gene. BRCA1 and BRCA2 are the genes most commonly associated with inherited breast cancer; however, mutations in TP53 and PTEN cause Li-Fraumeni syndrome and Cowden syndrome, respectively, both of which are associated with high lifetime risks of breast cancer. Advances in the field of breast cancer genetics have led to an improved understanding of detection and prevention strategies. More recently, strategies to target the underlying genetic defects in BRCA1- and BRCA2-associated breast and ovarian cancers are emerging and may have implications for certain types of sporadic breast cancer.

Article Info
Journal
Hematology/oncology clinics of North America
Abbr.
Hematol Oncol Clin North Am
Published
2011-01-21
Indexed
2010-09-06
Updated
2016-11-25
Language
English
Country/Region
United States
NLM ID
8709473
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