Literature DB >> 18431737

MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases.

Stefanie Engert1, Barbara Wappenschmidt, Beate Betz, Karin Kast, Michael Kutsche, Heide Hellebrand, Timm O Goecke, Marion Kiechle, Dieter Niederacher, Rita K Schmutzler, Alfons Meindl.   

Abstract

We present a comprehensive analysis of 1,506 German families for large genomic rearrangements (LGRs) in the BRCA1 gene and of 450 families in the BRCA2 gene by the multiplex ligation-dependent probe amplification (MLPA) technique. A total of 32 pathogenic rearrangements in the BRCA1 gene were found, accounting for 1.6% of all mutations, but for 9.6% of all BRCA1 mutations identified in a total of 1,996 families, including 490 with small pathogenic BRCA1/2 mutations. Considering only high risk groups for hereditary breast/ovarian cancer, the prevalence of rearrangements is 2.1%. Interestingly, deletions involving exon 17 of the BRCA1 gene seem to be most frequent in Germany. Apart from recurrent aberrations like del ex17, dupl ex13, and del ex22, accounting for more than 50% of all BRCA1 LGRs, we could fully characterize 11 novel deletions. Moreover, one novel deletion involving exons 1-7 and one deletion affecting the entire BRCA1 gene were identified. All rearrangements were detected in families with: 1) at least two breast cancer cases prior to the age of 51 years; 2) breast and ovarian cancer cases; 3) ovarian cancer only families with at least two ovarian cancer cases; or 4) a single breast cancer case prior to the age of 36 years, while no mutations were detected in breast cancer only families with no or only one breast cancer case prior to the age of 51 years. Analysis for gross rearrangements in 412 high-risk individuals, revealed no event in the BRCA2 gene and only two known CHEK2 mutations. However, in an additional 38 high-risk families with cooccurrence of female breast/ovarian and male breast cancer, one rearrangement in the BRCA2 gene was found. In summary, we advise restricting BRCA1 MLPA screening to those subgroups that revealed LGRs and recommend BRCA2 MLPA screening only for families presenting with cooccurrence of female and male breast cancer.

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Year:  2008        PMID: 18431737     DOI: 10.1002/humu.20723

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  28 in total

1.  Identification of germline genomic copy number variation in familial pancreatic cancer.

Authors:  Wigdan Al-Sukhni; Sarah Joe; Anath C Lionel; Nora Zwingerman; George Zogopoulos; Christian R Marshall; Ayelet Borgida; Spring Holter; Aaron Gropper; Sara Moore; Melissa Bondy; Alison P Klein; Gloria M Petersen; Kari G Rabe; Ann G Schwartz; Sapna Syngal; Stephen W Scherer; Steven Gallinger
Journal:  Hum Genet       Date:  2012-06-05       Impact factor: 4.132

2.  Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families.

Authors:  S M Schneegans; A Rosenberger; U Engel; M Sander; G Emons; M Shoukier
Journal:  Fam Cancer       Date:  2012-06       Impact factor: 2.375

3.  Large genomic rearrangement of BRCA1 and BRCA2 genes in familial breast cancer patients in Korea.

Authors:  Ja Young Cho; Dae-Yeon Cho; Sei Hyun Ahn; Su-Youn Choi; Inkyung Shin; Hyun Gyu Park; Jong Won Lee; Hee Jeong Kim; Jong Han Yu; Beom Seok Ko; Bo Kyung Ku; Byung Ho Son
Journal:  Fam Cancer       Date:  2014-06       Impact factor: 2.375

4.  Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.

Authors:  Alfons Meindl; Heide Hellebrand; Constanze Wiek; Verena Erven; Barbara Wappenschmidt; Dieter Niederacher; Marcel Freund; Peter Lichtner; Linda Hartmann; Heiner Schaal; Juliane Ramser; Ellen Honisch; Christian Kubisch; Hans E Wichmann; Karin Kast; Helmut Deissler; Christoph Engel; Bertram Müller-Myhsok; Kornelia Neveling; Marion Kiechle; Christopher G Mathew; Detlev Schindler; Rita K Schmutzler; Helmut Hanenberg
Journal:  Nat Genet       Date:  2010-04-18       Impact factor: 38.330

5.  Large genomic rearrangements in the familial breast and ovarian cancer gene BRCA1 are associated with an increased frequency of high risk features.

Authors:  Paul A James; Sarah Sawyer; Samantha Boyle; Mary-Anne Young; Serguei Kovalenko; Rebecca Doherty; Joanne McKinley; Kathryn Alsop; Victoria Beshay; Marion Harris; Stephen Fox; Geoffrey J Lindeman; Gillian Mitchell
Journal:  Fam Cancer       Date:  2015-06       Impact factor: 2.375

6.  The deletion of exons 3-5 of BRCA1 is the first founder rearrangement identified in breast and/or ovarian cancer Spanish families.

Authors:  Sarai Palanca; Inmaculada de Juan; Gema Perez-Simó; Eva Barragán; Isabel Chirivella; Eduardo Martínez; Oscar Fuster; Pascual Bolufer
Journal:  Fam Cancer       Date:  2013-03       Impact factor: 2.375

Review 7.  Ovarian cancer: in search of better marker systems based on DNA repair defects.

Authors:  Dominic Varga; Miriam Deniz; Lukas Schwentner; Lisa Wiesmüller
Journal:  Int J Mol Sci       Date:  2013-01-04       Impact factor: 5.923

8.  Accounting for uncertainty when assessing association between copy number and disease: a latent class model.

Authors:  Juan R González; Isaac Subirana; Geòrgia Escaramís; Solymar Peraza; Alejandro Cáceres; Xavier Estivill; Lluís Armengol
Journal:  BMC Bioinformatics       Date:  2009-06-06       Impact factor: 3.169

9.  A novel BRCA1 duplication and new insights on the spectrum and frequency of germline large genomic rearrangements in BRCA1/BRCA2.

Authors:  Ibrahim Sahin; Hanife Saat
Journal:  Mol Biol Rep       Date:  2021-06-19       Impact factor: 2.316

10.  Seventeen years after BRCA1: what is the BRCA mutation status of the breast cancer patients in Africa? - a systematic review.

Authors:  Lawal Abdulrazzaq Oluwagbemiga; Atoyebi Oluwole; Adesunkanmi Abdulrasheed Kayode
Journal:  Springerplus       Date:  2012-12-28
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