Literature DB >> 22652533

A Finnish founder mutation in RAD51D: analysis in breast, ovarian, prostate, and colorectal cancer.

Liisa M Pelttari1, Johanna Kiiski, Riikka Nurminen, Anne Kallioniemi, Johanna Schleutker, Alexandra Gylfe, Lauri A Aaltonen, Arto Leminen, Päivi Heikkilä, Carl Blomqvist, Ralf Bützow, Kristiina Aittomäki, Heli Nevanlinna.   

Abstract

BACKGROUND: RAD51D and RAD54L are involved in homologous recombination, and rare mutations in RAD51D were recently found in breast-ovarian cancer families. This study investigated RAD51D and RAD54L for mutations in breast and ovarian cancer patients in the Finnish population.
METHODS: The study sequenced the RAD51D and RAD54L genes in 95 breast and/or ovarian cancer families and genotyped the identified mutation in an additional 2200 breast and 553 ovarian cancer patients and 2102 population controls. To investigate the role of the mutation in other common cancers, 1094 prostate and 980 colorectal cancer patients were genotyped.
RESULTS: In the screening of RAD51D, one deleterious founder mutation c.576+1G>A was identified in two breast-ovarian cancer families. No mutations were found in RAD54L. Altogether, the c.576+1G>A mutation was detected in 5/707 patients with a personal or family history of ovarian cancer (OR 9.16, 95% CI 1.07 to 78.56; p=0.024), with the highest frequency among breast-ovarian cancer families (3/105 vs 1/1287 controls, OR 37.82, 95% CI 3.90 to 366.91; p=0.0016), but no elevated frequency among breast cancer patients/families (2/2105, p=1). The mutation was not found among prostate or colorectal cancer patients.
CONCLUSIONS: The results of this study on familial and unselected breast, ovarian, colorectal, and prostate cancer patients suggest that RAD51D is primarily a moderate penetrance susceptibility gene for ovarian cancer, with clinical significance for the carriers.

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Year:  2012        PMID: 22652533      PMCID: PMC5426530          DOI: 10.1136/jmedgenet-2012-100852

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  16 in total

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Authors:  Pia Vahteristo; Jirina Bartkova; Hannaleena Eerola; Kirsi Syrjäkoski; Salla Ojala; Outi Kilpivaara; Anitta Tamminen; Juha Kononen; Kristiina Aittomäki; Päivi Heikkilä; Kaija Holli; Carl Blomqvist; Jiri Bartek; Olli-P Kallioniemi; Heli Nevanlinna
Journal:  Am J Hum Genet       Date:  2002-07-28       Impact factor: 11.025

2.  Ten genes for inherited breast cancer.

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3.  RAD51C is a susceptibility gene for ovarian cancer.

Authors:  Liisa M Pelttari; Tuomas Heikkinen; Deborah Thompson; Anne Kallioniemi; Johanna Schleutker; Kaija Holli; Carl Blomqvist; Kristiina Aittomäki; Ralf Bützow; Heli Nevanlinna
Journal:  Hum Mol Genet       Date:  2011-05-25       Impact factor: 6.150

Review 4.  Functions of the Snf2/Swi2 family Rad54 motor protein in homologous recombination.

Authors:  Shannon J Ceballos; Wolf-Dietrich Heyer
Journal:  Biochim Biophys Acta       Date:  2011-06-16

Review 5.  Models of genetic susceptibility to breast cancer.

Authors:  A C Antoniou; D F Easton
Journal:  Oncogene       Date:  2006-09-25       Impact factor: 9.867

6.  Mutation of the RAD51C gene in a Fanconi anemia-like disorder.

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Journal:  Nat Genet       Date:  2010-04-18       Impact factor: 38.330

7.  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

8.  Variation in cancer risks, by mutation position, in BRCA2 mutation carriers.

Authors:  D Thompson; D Easton
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9.  A recurrent mutation in PALB2 in Finnish cancer families.

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Journal:  Nature       Date:  2007-02-07       Impact factor: 49.962

10.  BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients.

Authors:  Z Kote-Jarai; D Leongamornlert; E Saunders; M Tymrakiewicz; E Castro; N Mahmud; M Guy; S Edwards; L O'Brien; E Sawyer; A Hall; R Wilkinson; T Dadaev; C Goh; D Easton; D Goldgar; R Eeles
Journal:  Br J Cancer       Date:  2011-09-27       Impact factor: 7.640

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  21 in total

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Authors:  Irene Konstanta; Florentia Fostira; Paraskevi Apostolou; Efstratios Stratikos; Despoina Kalfakakou; Andreas Pampanos; Panagoula Kollia; Christos Papadimitriou; Irene Konstantopoulou; Drakoulis Yannoukakos
Journal:  J Hum Genet       Date:  2018-08-15       Impact factor: 3.172

2.  RNF138 interacts with RAD51D and is required for DNA interstrand crosslink repair and maintaining chromosome integrity.

Authors:  Brian D Yard; Nicole M Reilly; Michael K Bedenbaugh; Douglas L Pittman
Journal:  DNA Repair (Amst)       Date:  2016-04-21

3.  Inherited Mutations in Women With Ovarian Carcinoma.

Authors:  Barbara M Norquist; Maria I Harrell; Mark F Brady; Tom Walsh; Ming K Lee; Suleyman Gulsuner; Sarah S Bernards; Silvia Casadei; Qian Yi; Robert A Burger; John K Chan; Susan A Davidson; Robert S Mannel; Paul A DiSilvestro; Heather A Lankes; Nilsa C Ramirez; Mary Claire King; Elizabeth M Swisher; Michael J Birrer
Journal:  JAMA Oncol       Date:  2016-04       Impact factor: 31.777

4.  Screening of HELQ in breast and ovarian cancer families.

Authors:  Liisa M Pelttari; Laura Kinnunen; Johanna I Kiiski; Sofia Khan; Carl Blomqvist; Kristiina Aittomäki; Heli Nevanlinna
Journal:  Fam Cancer       Date:  2016-01       Impact factor: 2.375

5.  Gene-panel sequencing and the prediction of breast-cancer risk.

Authors:  Douglas F Easton; Paul D P Pharoah; Antonis C Antoniou; Marc Tischkowitz; Sean V Tavtigian; Katherine L Nathanson; Peter Devilee; Alfons Meindl; Fergus J Couch; Melissa Southey; David E Goldgar; D Gareth R Evans; Georgia Chenevix-Trench; Nazneen Rahman; Mark Robson; Susan M Domchek; William D Foulkes
Journal:  N Engl J Med       Date:  2015-05-27       Impact factor: 91.245

6.  Rare coding variants in DNA damage repair genes associated with timing of natural menopause.

Authors:  Lucas D Ward; Margaret M Parker; Aimee M Deaton; Ho-Chou Tu; Alexander O Flynn-Carroll; Gregory Hinkle; Paul Nioi
Journal:  HGG Adv       Date:  2021-12-22

7.  Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic.

Authors:  Marketa Janatova; Jana Soukupova; Jana Stribrna; Petra Kleiblova; Michal Vocka; Petra Boudova; Zdenek Kleibl; Petr Pohlreich
Journal:  PLoS One       Date:  2015-06-09       Impact factor: 3.240

Review 8.  Hereditary breast cancer: the era of new susceptibility genes.

Authors:  Paraskevi Apostolou; Florentia Fostira
Journal:  Biomed Res Int       Date:  2013-03-21       Impact factor: 3.411

9.  Analysis of RAD51D in ovarian cancer patients and families with a history of ovarian or breast cancer.

Authors:  Ella R Thompson; Simone M Rowley; Sarah Sawyer; Diana M Eccles; Alison H Trainer; Gillian Mitchell; Paul A James; Ian G Campbell
Journal:  PLoS One       Date:  2013-01-25       Impact factor: 3.240

10.  RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families.

Authors:  Liisa M Pelttari; Johanna I Kiiski; Salla Ranta; Sara Vilske; Carl Blomqvist; Kristiina Aittomäki; Heli Nevanlinna
Journal:  Springerplus       Date:  2015-02-24
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