Identification of a common polymorphism in the TopBP1 gene associated with hereditary susceptibility to breast and ovarian cancer

被引:31
|
作者
Karppinen, Sanna-Maria
Erkko, Hannele
Reini, Kaarina
Pospiech, Helmut
Heikkinen, Katri
Rapakko, Katrin
Syvaoja, Juhani E.
Winqvist, Robert
机构
[1] Oulu Univ Hosp, Dept Clin Genet, FIN-90029 Oys, Finland
[2] Univ Oulu, Bioctr Oulu, FIN-90014 Oulu, Finland
[3] Univ Oulu, Dept Biochem, FIN-90014 Oulu, Finland
[4] Univ Joensuu, Dept Biol, FIN-80101 Joensuu, Finland
基金
芬兰科学院;
关键词
TopBP1; hereditary susceptibility; cell cycle checkpoint; DNA repair;
D O I
10.1016/j.ejca.2006.05.030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Besides BRCA1 and BRCA2 other genes are also likely to be involved in hereditary predisposition to breast and/or ovarian cancer. TopBP1 (topoisomerase II beta binding protein 1) displays sequence homology as well as functional similarities with BRCA1, and the two proteins have been suggested to function partly in the same cellular processes. TopBP1 is crucial for DNA damage and replication checkpoint controls. Based on its biological significance, we reasoned that TopBP1 is a plausible susceptibility gene for hereditary breast and/or ovarian cancer and therefore screened affected index cases from 125 Finnish cancer families for germline changes by conformation sensitive gel electrophoresis (CSGE). Altogether 19 different sequence alterations were detected. A novel heterozygous Arg309Cys variant was observed at elevated frequency in the familial cancer cases compared to healthy controls (15.2% versus 7.0%; P = 0.002). Current results suggest that Arg309Cys is a commonly occurring germline alteration possibly associated with a slightly increased breast and/or ovarian cancer risk. This is the first study reporting mutation screening of the TopBP1 gene in a familial cancer material. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2647 / 2652
页数:6
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