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Record W2131786456 · doi:10.1371/journal.pgen.1004256

DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

2014· article· en· W2131786456 on OpenAlexafffund
Ana Osório, Roger L. Milne, Karoline Kuchenbaecker, Tereza Vaclová, Guillermo Pita, Rosario Alonso, Paolo Peterlongo, Ignacio Blanco, M. Durán, Orland Dı́ez, Teresa Ramón y Cajal, Irene Konstantopoulou, Cristina Martínez-Bouzas, Raquel Andrés Conejero, Penny Soucy, Lesley McGuffog, Daniel Barrowdale, Andrew Lee, Brita Arver, Johanna Rantala, Niklas Loman, Hans Ehrencrona, Olufunmilayo I. Olopade, Mary Beattie, Susan M. Domchek, Katherine L. Nathanson, Timothy R. Rebbeck, Banu Arun, Beth Y. Karlan, Christine Walsh, Jenny Lester, Esther M. John, Alice S. Whittemore, Mary B. Daly, Melissa C. Southey, John L. Hopper, Mary Beth Terry, Saundra S. Buys, Ramūnas Janavičius, Cecilia M. Dorfling, Elizabeth J. van Rensburg, Linda Steele, Susan L. Neuhausen, Yuan Chun Ding, Thomas van Overeem Hansen, Lars Jønson, Bent Ejlertsen, Anne‐Marie Gerdes, Mar Infante, Belén Herráez, Leticia Thais Moreno, Jeffrey N. Weitzel, Josef Herzog, Kisa Weeman, Siranoush Manoukian, Bernard Peissel, Daniela Zaffaroni, Giulietta Scuvera, Bernardo Bonanni, Frédérique Mariette, Sara Volorio, Alessandra Viel, Liliana Varesco, Laura Papi, Laura Ottini, Maria Grazia Tibiletti, Paolo Radice, Drakoulis Yannoukakos, Judy Garber, Debra Frost, Radka Platte, Elena Fineberg, D. Gareth Evans, Fiona Lalloo, Louise Izatt, Rosalind A. Eeles, Julian Adlard, Rosemarie Davidson, Trevor Cole, Diana Eccles, Jackie Cook, Shirley Hodgson, Carole Brewer, Marc Tischkowitz, Fiona Douglas, Mary Porteous, Lucy Side, Lisa Walker, Patrick J. Morrison, Alan Donaldson, John Kennedy, Claire Foo, Andrew K. Godwin, Rita K. Schmutzler, Barbara Wappenschmidt, Kerstin Rhiem, Christoph Engel, Alfons Meindl, Nina Ditsch, Norbert Arnold, Hans Jörg Plendl, Dieter Niederacher, Christian Sutter, Shan Wang‐Gohrke, Doris Steinemann, Sabine Preisler-Adams, Karin Kast, Raymonda Varon-Mateeva, Andrea Gehrig, Dominique Stoppa‐Lyonnet, Olga M. Sinilnikova, Sylvie Mazoyer, Francesca Damiola, Bruce Poppe, Kathleen Claes, Marion Piedmonte, Kathy Tucker, Floor Backes, Gustavo C. Rodriguez, Wendy R. Brewster, Katie Wakeley, Thomas Rutherford, Heli Nevanlinna, Kristiina Aittomäki, Matti A. Rookus, Theo A.M. van Os, Lizet van der Kolk, Jeffrey L. Lange, Hanne Meijers‐Heijboer, Annemarie H. van der Hout, Christi J. van Asperen, E. Gómez, J. Margriet Collée, Carolien H. M. van Deurzen, Rob B. van der Luijt, Peter Devilee, Edith Oláh, Conxi Lázaro, Àlex Teulé, Mireia Menéndez, Anna Jakubowska, Cezary Cybulski, Jacek Gronwald, Jan Lubiński, Katarzyna Durda, Katarzyna Jaworska–Bieniek, Oskar T. Johannsson, Christine Maugard, Marco Montagna, Silvia Tognazzo, Manuel R. Teixeira, Sue Healey, Curtis Olswold, Lucia Guidugli, Noralane M. Lindor, Susan Slager, Csilla I. Szabo, Joseph Vijai, Mark E. Robson, Noah D. Kauff, Liying Zhang, Rohini Rau‐Murthy, A. Fink-Retter, Christian F. Singer, Christine Rappaport, Daphne Geschwantler Kaulich, Georg Pfeiler, Muy-Kheng Tea, Andreas Berger, Catherine M. Phelan, Mark H. Greene, Flavio Lejbkowicz, Irene L. Andrulis, Anna Marie Mulligan, Gord Glendon, Amanda E. Toland, Anders Bojesen, Inge Søkilde Pedersen, Lone Sunde, Mads Thomassen, Torben A. Kruse, Uffe Birk Jensen, Eitan Friedman, Yael Laitman, Shani Paluch Shimon, Jacques Simard, Douglas F. Easton, Kenneth Offit, Fergus J. Couch, Georgia Chenevix‐Trench, Antonis C. Antoniou, Javier Benı́tez

Bibliographic record

VenuePLoS Genetics · 2014
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBRCA gene mutations in cancer
Canadian institutionsCancer Care OntarioUniversity Health NetworkUniversity of TorontoLunenfeld-Tanenbaum Research InstituteMount Sinai HospitalUniversité LavalCentre hospitalier universitaire de Québec
FundersNational Center for Advancing Translational SciencesMedical Research CouncilCanadian Institutes of Health ResearchCancer Center, University of KansasNational Institutes of HealthMinistero dello Sviluppo EconomicoFox Chase Cancer CenterUppsala UniversitetAssociazione Italiana per la Ricerca sul CancroBeckman Research Institute, City of HopeCancer Research UKKWF KankerbestrijdingNIH Office of the DirectorDeutsche KrebshilfeNational Cancer InstituteLandspítali HáskólasjúkrahúsHungarian Scientific Research FundLunds UniversitetSahlgrenska UniversitetssjukhusetNederlandse Organisatie voor Wetenschappelijk OnderzoekNational Breast Cancer FoundationEuropean CommissionMinistère du Développement Économique, de l’Innovation et de l’ExportationNational Institute for Health and Care ResearchUniversity of ChicagoInstituto de Salud Carlos IIIHope Funds for Cancer ResearchRoyal Marsden NHS Foundation TrustMcGill UniversityEuropean Social FundCanadian Breast Cancer Research AllianceState Education Development Agency Republic of LatviaHelsingin ja Uudenmaan SairaanhoitopiiriUniversity of California, San FranciscoMinistero della SaluteNational Health and Medical Research CouncilKansas Bioscience Authority
KeywordsDNA glycosylaseBiologyMUTYHDNA repairBase excision repairGeneticsSingle-nucleotide polymorphismCancerMutationBreast cancerCancer researchGeneGenotype

Abstract

fetched live from OpenAlex

Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathway could be associated with cancer risk in carriers of mutations in the high-penetrance susceptibility genes BRCA1 and BRCA2, given the relation of synthetic lethality that exists between one of the components of the BER pathway, PARP1 (poly ADP ribose polymerase), and both BRCA1 and BRCA2. In the present study, we have performed a comprehensive analysis of 18 genes involved in BER using a tagging SNP approach in a large series of BRCA1 and BRCA2 mutation carriers. 144 SNPs were analyzed in a two stage study involving 23,463 carriers from the CIMBA consortium (the Consortium of Investigators of Modifiers of BRCA1 and BRCA2). Eleven SNPs showed evidence of association with breast and/or ovarian cancer at p<0.05 in the combined analysis. Four of the five genes for which strongest evidence of association was observed were DNA glycosylases. The strongest evidence was for rs1466785 in the NEIL2 (endonuclease VIII-like 2) gene (HR: 1.09, 95% CI (1.03-1.16), p = 2.7 × 10(-3)) for association with breast cancer risk in BRCA2 mutation carriers, and rs2304277 in the OGG1 (8-guanine DNA glycosylase) gene, with ovarian cancer risk in BRCA1 mutation carriers (HR: 1.12 95%CI: 1.03-1.21, p = 4.8 × 10(-3)). DNA glycosylases involved in the first steps of the BER pathway may be associated with cancer risk in BRCA1/2 mutation carriers and should be more comprehensively studied.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.596
Threshold uncertainty score0.854

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.015
GPT teacher head0.255
Teacher spread0.240 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations130
Published2014
Admission routes2
Has abstractyes

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