Title: |
BRCA1 and BRCA2 mutation analysis in breast‐ovarian cancer families from northeastern PolandCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #610 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/610.pdf |
Authors: |
Magdalena Perkowska, Izabela BroŻek, Barbara Wysocka, Karin Haraldsson, Therese Sandberg, Ulla Johansson, Gunilla Sellberg, Ake Borg, Janusz Limon |
Source: |
Human Mutation; May2003, Vol. 21 Issue 5, p553-554, 2p |
Subject Terms: |
GENETICS of breast cancer, OVARIAN cancer, OVARIAN diseases, GENETIC mutation, HUMAN genetics, GENETIC testing, GERM cells, GENETICS |
Geographic Terms: |
POLAND |
Abstract: |
Sixty high‐risk breast and/or ovarian cancer families from North‐Eastern Poland were screened for germline mutations in BRCA1 (MIM# 113705) and BRCA2 (MIM# 600185), using a combination of protein truncation test, denaturing high‐performance liquid chromatography and direct sequencing. Sixteen (27%) of the families were found to carry nine different BRCA mutations, including 14 families with BRCA1 mutation and two families with BRCA2 mutation. The results suggest the presence of two strong BRCA1 founder mutations in the Polish population – 5382insC (6 families) and 300T>G (Cys61Gly; 3 families). The remaining seven mutations were found in single families and included three previously reported BRCA1 mutations (185delAG, 2682C>T [Gln855Ter] and 3819del5), a novel BRCA1 mutation (IVS14+1G>A), as well as two BRCA2 mutations (4088delA and 7985G>A [Trp2586Ter]) not previously observed in Polish families. We confirm the strong influence of two Central‐Eastern European BRCA1 founder mutations in familial breast and/or ovarian cancer in Poland. We also conclude that the Polish population has a more dispersed BRCA mutation spectrum than had been earlier thought. This warrants further careful BRCA mutation screening in order to optimise genetic counselling and disease prevention in affected families. © 2003 Wiley‐Liss, Inc. [ABSTRACT FROM AUTHOR] |
|
Copyright of Human Mutation is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
Database: |
Complementary Index |