Literature DB >> 20652397

The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers.

Irene Catucci1, Paolo Verderio, Sara Pizzamiglio, Siranoush Manoukian, Bernard Peissel, Daniela Zaffaroni, Gaia Roversi, Carla B Ripamonti, Barbara Pasini, Monica Barile, Alessandra Viel, Giuseppe Giannini, Laura Papi, Liliana Varesco, Aline Martayan, Mirko Riboni, Sara Volorio, Paolo Radice, Paolo Peterlongo.   

Abstract

The rs3834129 polymorphism, in the promoter of CASP8 gene, has been recently reported as associated with breast cancer risk in the general population, with the minor allele del having a protective effect. Some of the genetic variants found associated with breast cancer risk were reported as risk modifiers in individuals with mutations in BRCA1 and BRCA2 genes. Here, we tested the effect of the rs3834129 del allele on breast cancer risk in BRCA mutation carriers. The rs3834129 was genotyped in a total of 1,207 Italian female BRCA mutation carriers. Of these, 740 carried a BRCA1 mutation and 467 a BRCA2 mutation. Overall, 699 were affected with breast cancer and 508 were unaffected. When considering class 1 (loss-of-function) BRCA mutations, hazard ratios estimated by weighted multivariable Cox regression model, for individuals with at least one copy of the del allele, were 1.46 (95% confidence interval (CI): 1.08-1.99) for BRCA1 and BRCA2 mutation carriers combined, 1.74 (95% CI: 1.24-2.46) for BRCA1 mutation carriers, and 1.09 (95% CI: 0.66-1.80) for BRCA2 mutation carriers. These results suggest that the minor allele del of rs3834129 is associated under a dominant model with increased breast cancer risk in carriers of BRCA1 mutations but not in carriers of BRCA2 mutations.

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Year:  2010        PMID: 20652397     DOI: 10.1007/s10549-010-1068-8

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  5 in total

1.  Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Authors:  Antonis C Antoniou; Christiana Kartsonaki; Olga M Sinilnikova; Penny Soucy; Lesley McGuffog; Sue Healey; Andrew Lee; Paolo Peterlongo; Siranoush Manoukian; Bernard Peissel; Daniela Zaffaroni; Elisa Cattaneo; Monica Barile; Valeria Pensotti; Barbara Pasini; Riccardo Dolcetti; Giuseppe Giannini; Anna Laura Putignano; Liliana Varesco; Paolo Radice; Phuong L Mai; Mark H Greene; Irene L Andrulis; Gord Glendon; Hilmi Ozcelik; Mads Thomassen; Anne-Marie Gerdes; Torben A Kruse; Uffe Birk Jensen; Dorthe G Crüger; Maria A Caligo; Yael Laitman; Roni Milgrom; Bella Kaufman; Shani Paluch-Shimon; Eitan Friedman; Niklas Loman; Katja Harbst; Annika Lindblom; Brita Arver; Hans Ehrencrona; Beatrice Melin; Katherine L Nathanson; Susan M Domchek; Timothy Rebbeck; Ania Jakubowska; Jan Lubinski; Jacek Gronwald; Tomasz Huzarski; Tomasz Byrski; Cezary Cybulski; Bohdan Gorski; Ana Osorio; Teresa Ramón y Cajal; Florentia Fostira; Raquel Andrés; Javier Benitez; Ute Hamann; Frans B Hogervorst; Matti A Rookus; Maartje J Hooning; Marcel R Nelen; Rob B van der Luijt; Theo A M van Os; Christi J van Asperen; Peter Devilee; Hanne E J Meijers-Heijboer; Encarna B Gómez Garcia; Susan Peock; Margaret Cook; Debra Frost; Radka Platte; Jean Leyland; D Gareth Evans; Fiona Lalloo; Ros Eeles; Louise Izatt; Julian Adlard; Rosemarie Davidson; Diana Eccles; Kai-ren Ong; Jackie Cook; Fiona Douglas; Joan Paterson; M John Kennedy; Zosia Miedzybrodzka; Andrew Godwin; Dominique Stoppa-Lyonnet; Bruno Buecher; Muriel Belotti; Carole Tirapo; Sylvie Mazoyer; Laure Barjhoux; Christine Lasset; Dominique Leroux; Laurence Faivre; Myriam Bronner; Fabienne Prieur; Catherine Nogues; Etienne Rouleau; Pascal Pujol; Isabelle Coupier; Marc Frénay; John L Hopper; Mary B Daly; Mary B Terry; Esther M John; Saundra S Buys; Yosuf Yassin; Alexander Miron; David Goldgar; Christian F Singer; Muy-Kheng Tea; Georg Pfeiler; Anne Catharina Dressler; Thomas v O Hansen; Lars Jønson; Bent Ejlertsen; Rosa Bjork Barkardottir; Tomas Kirchhoff; Kenneth Offit; Marion Piedmonte; Gustavo Rodriguez; Laurie Small; John Boggess; Stephanie Blank; Jack Basil; Masoud Azodi; Amanda Ewart Toland; Marco Montagna; Silvia Tognazzo; Simona Agata; Evgeny Imyanitov; Ramunas Janavicius; Conxi Lazaro; Ignacio Blanco; Paul D P Pharoah; Lara Sucheston; Beth Y Karlan; Christine S Walsh; Edith Olah; Aniko Bozsik; Soo-Hwang Teo; Joyce L Seldon; Mary S Beattie; Elizabeth J van Rensburg; Michelle D Sluiter; Orland Diez; Rita K Schmutzler; Barbara Wappenschmidt; Christoph Engel; Alfons Meindl; Ina Ruehl; Raymonda Varon-Mateeva; Karin Kast; Helmut Deissler; Dieter Niederacher; Norbert Arnold; Dorothea Gadzicki; Ines Schönbuchner; Trinidad Caldes; Miguel de la Hoya; Heli Nevanlinna; Kristiina Aittomäki; Martine Dumont; Jocelyne Chiquette; Marc Tischkowitz; Xiaoqing Chen; Jonathan Beesley; Amanda B Spurdle; Susan L Neuhausen; Yuan Chun Ding; Zachary Fredericksen; Xianshu Wang; Vernon S Pankratz; Fergus Couch; Jacques Simard; Douglas F Easton; Georgia Chenevix-Trench
Journal:  Hum Mol Genet       Date:  2011-05-18       Impact factor: 6.150

2.  Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.

Authors:  Mia M Gaudet; Tomas Kirchhoff; Todd Green; Joseph Vijai; Joshua M Korn; Candace Guiducci; Ayellet V Segrè; Kate McGee; Lesley McGuffog; Christiana Kartsonaki; Jonathan Morrison; Sue Healey; Olga M Sinilnikova; Dominique Stoppa-Lyonnet; Sylvie Mazoyer; Marion Gauthier-Villars; Hagay Sobol; Michel Longy; Marc Frenay; Frans B L Hogervorst; Matti A Rookus; J Margriet Collée; Nicoline Hoogerbrugge; Kees E P van Roozendaal; Marion Piedmonte; Wendy Rubinstein; Stacy Nerenstone; Linda Van Le; Stephanie V Blank; Trinidad Caldés; Miguel de la Hoya; Heli Nevanlinna; Kristiina Aittomäki; Conxi Lazaro; Ignacio Blanco; Adalgeir Arason; Oskar T Johannsson; Rosa B Barkardottir; Peter Devilee; Olofunmilayo I Olopade; Susan L Neuhausen; Xianshu Wang; Zachary S Fredericksen; Paolo Peterlongo; Siranoush Manoukian; Monica Barile; Alessandra Viel; Paolo Radice; Catherine M Phelan; Steven Narod; Gad Rennert; Flavio Lejbkowicz; Anath Flugelman; Irene L Andrulis; Gord Glendon; Hilmi Ozcelik; Amanda E Toland; Marco Montagna; Emma D'Andrea; Eitan Friedman; Yael Laitman; Ake Borg; Mary Beattie; Susan J Ramus; Susan M Domchek; Katherine L Nathanson; Tim Rebbeck; Amanda B Spurdle; Xiaoqing Chen; Helene Holland; Esther M John; John L Hopper; Saundra S Buys; Mary B Daly; Melissa C Southey; Mary Beth Terry; Nadine Tung; Thomas V Overeem Hansen; Finn C Nielsen; Mark H Greene; Mark I Greene; Phuong L Mai; Ana Osorio; Mercedes Durán; Raquel Andres; Javier Benítez; Jeffrey N Weitzel; Judy Garber; Ute Hamann; Susan Peock; Margaret Cook; Clare Oliver; Debra Frost; Radka Platte; D Gareth Evans; Fiona Lalloo; Ros Eeles; Louise Izatt; Lisa Walker; Jacqueline Eason; Julian Barwell; Andrew K Godwin; Rita K Schmutzler; Barbara Wappenschmidt; Stefanie Engert; Norbert Arnold; Dorothea Gadzicki; Michael Dean; Bert Gold; Robert J Klein; Fergus J Couch; Georgia Chenevix-Trench; Douglas F Easton; Mark J Daly; Antonis C Antoniou; David M Altshuler; Kenneth Offit
Journal:  PLoS Genet       Date:  2010-10-28       Impact factor: 5.917

3.  Ten modifiers of BRCA1 penetrance validated in a Norwegian series.

Authors:  Cecilie Heramb; Per Olaf Ekstrøm; Kukatharmini Tharmaratnam; Eivind Hovig; Pål Møller; Lovise Mæhle
Journal:  Hered Cancer Clin Pract       Date:  2015-05-30       Impact factor: 2.857

4.  DOTS-Finder: a comprehensive tool for assessing driver genes in cancer genomes.

Authors:  Giorgio Em Melloni; Alessandro Ge Ogier; Stefano de Pretis; Luca Mazzarella; Mattia Pelizzola; Pier Giuseppe Pelicci; Laura Riva
Journal:  Genome Med       Date:  2014-06-10       Impact factor: 11.117

5.  Evaluation of single nucleotide polymorphisms in microRNAs (hsa-miR-196a2 rs11614913 C/T) from Brazilian women with breast cancer.

Authors:  José Juvenal Linhares; Marcos Azevedo; Adalberto Abraão Siufi; Cristina Valleta de Carvalho; Maria Del Carmen Garcia Molina Wolgien; Emmanuelle Coelho Noronha; Tatiana Carvalho de Souza Bonetti; Ismael Dale Cotrim Guerreiro da Silva
Journal:  BMC Med Genet       Date:  2012-12-10       Impact factor: 2.103

  5 in total

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