Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
Paolo Peterlongo,
Jenny Chang-Claude,
Kirsten B Moysich,
Anja Rudolph,
Rita K Schmutzler,
Jacques Simard,
Penny Soucy,
Rosalind A Eeles,
Douglas F Easton,
Ute Hamann,
Stefan Wilkening,
Bowang Chen,
Matti A Rookus,
Marjanka K Schmidt,
Frederieke H van der Baan,
Amanda B Spurdle,
Logan C Walker,
Felicity Lose,
Ana-Teresa Maia,
Marco Montagna,
Laura Matricardi,
Jan Lubinski,
Anna Jakubowska,
Encarna B Gómez Garcia,
Olufunmilayo I Olopade,
Robert L Nussbaum,
Katherine L Nathanson,
Susan M Domchek,
Timothy R Rebbeck,
Banu K Arun,
Beth Y Karlan,
Sandra Orsulic,
Jenny Lester,
Wendy K Chung,
Alex Miron,
Melissa C Southey,
David E Goldgar,
Saundra S Buys,
Ramunas Janavicius,
Cecilia M Dorfling,
Elizabeth J van Rensburg,
Yuan Chun Ding,
Susan L Neuhausen,
Thomas V O Hansen,
Anne-Marie Gerdes,
Bent Ejlertsen,
Lars Jønson,
Ana Osorio,
Cristina Martínez-Bouzas,
Javier Benitez,
Edye E Conway,
Kathleen R Blazer,
Jeffrey N Weitzel,
Siranoush Manoukian,
Bernard Peissel,
Daniela Zaffaroni,
Giulietta Scuvera,
Monica Barile,
Filomena Ficarazzi,
Frederique Mariette,
Stefano Fortuzzi,
Alessandra Viel,
Giuseppe Giannini,
Laura Papi,
Aline Martayan,
Maria Grazia Tibiletti,
Paolo Radice,
Athanassios Vratimos,
Florentia Fostira,
Judy E Garber,
Alan Donaldson,
Carole Brewer,
Claire Foo,
D Gareth R Evans,
Debra Frost,
Diana Eccles,
Angela Brady,
Jackie Cook,
Marc Tischkowitz,
Julian Adlard,
Julian Barwell,
Lisa Walker,
Louise Izatt,
Lucy E Side,
M John Kennedy,
Mark T Rogers,
Mary E Porteous,
Patrick J Morrison,
Radka Platte,
Rosemarie Davidson,
Shirley V Hodgson,
Steve Ellis,
Trevor Cole,
,
Andrew K Godwin,
Kathleen Claes,
Tom Van Maerken,
Alfons Meindl,
Andrea Gehrig,
Christian Sutter,
Christoph Engel,
Dieter Niederacher,
Doris Steinemann,
Hansjoerg Plendl,
Karin Kast,
Kerstin Rhiem,
Nina Ditsch,
Norbert Arnold,
Raymonda Varon-Mateeva,
Barbara Wappenschmidt,
Shan Wang-Gohrke,
Brigitte Bressac-de Paillerets,
Bruno Buecher,
Capucine Delnatte,
Claude Houdayer,
Dominique Stoppa-Lyonnet,
Francesca Damiola,
Isabelle Coupier,
Laure Barjhoux,
Laurence Venat-Bouvet,
Lisa Golmard,
Nadia Boutry-Kryza,
Olga M Sinilnikova,
Olivier Caron,
Pascal Pujol,
Sylvie Mazoyer,
Muriel Belotti,
,
Marion Piedmonte,
Michael L Friedlander,
Gustavo C Rodriguez,
Larry J Copeland,
Miguel de la Hoya,
Pedro Perez Segura,
Heli Nevanlinna,
Kristiina Aittomäki,
Theo A M van Os,
Hanne E J Meijers-Heijboer,
Annemarie H van der Hout,
Maaike P G Vreeswijk,
Nicoline Hoogerbrugge,
Margreet G E M Ausems,
Helena C van Doorn,
J Margriet Collée,
,
Edith Olah,
Orland Diez,
Ignacio Blanco,
Conxi Lazaro,
Joan Brunet,
Lidia Feliubadalo,
Cezary Cybulski,
Jacek Gronwald,
Katarzyna Durda,
Katarzyna Jaworska-Bieniek,
Grzegorz Sukiennicki,
Adalgeir Arason,
Jocelyne Chiquette,
Manuel R Teixeira,
Curtis Olswold,
Fergus J Couch,
Noralane M Lindor,
Xianshu Wang,
Csilla I Szabo,
Kenneth Offit,
Marina Corines,
Lauren Jacobs,
Mark E Robson,
Liying Zhang,
Vijai Joseph,
Andreas Berger,
Christian F Singer,
Christine Rappaport,
Daphne Geschwantler Kaulich,
Georg Pfeiler,
Muy-Kheng M Tea,
Catherine M Phelan,
Mark H Greene,
Phuong L Mai,
Gad Rennert,
Anna Marie Mulligan,
Gord Glendon,
Sandrine Tchatchou,
Irene L Andrulis,
Amanda Ewart Toland,
Anders Bojesen,
Inge Sokilde Pedersen,
Mads Thomassen,
Uffe Birk Jensen,
Yael Laitman,
Johanna Rantala,
Anna von Wachenfeldt,
Hans Ehrencrona,
Marie Stenmark Askmalm,
Åke Borg,
Karoline B Kuchenbaecker,
Lesley McGuffog,
Daniel Barrowdale,
Sue Healey,
Andrew Lee,
Paul D P Pharoah,
Georgia Chenevix-Trench,
,
Antonis C Antoniou,
Eitan Friedman
Abstract
METHODS
Genotyping data from 15,252 BRCA1 and 8,211 BRCA2 mutation carriers, for known variants (n = 3,248) located within or around 445 candidate genes, were available through the iCOGS custom-designed array. Breast and ovarian cancer association analysis was performed within a retrospective cohort approach.
CONCLUSION
There is little evidence that any of the evaluated candidate variants act as modifiers of breast and/or ovarian cancer risk in BRCA1 or BRCA2 mutation carriers.
RESULTS
The observed P values of association ranged between 0.005 and 1.000. None of the variants was significantly associated with breast or ovarian cancer risk in either BRCA1 or BRCA2 mutation carriers, after multiple testing adjustments.
BACKGROUND
BRCA1 and BRCA2 mutation carriers are at substantially increased risk for developing breast and ovarian cancer. The incomplete penetrance coupled with the variable age at diagnosis in carriers of the same mutation suggests the existence of genetic and nongenetic modifying factors. In this study, we evaluated the putative role of variants in many candidate modifier genes.
IMPACT
Genome-wide association studies have been more successful at identifying genetic modifiers of BRCA1/2 penetrance than candidate gene studies.
More about this publication
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology