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Record W2918113141 · doi:10.1038/s41416-019-0393-x

Genome-wide association study of germline variants and breast cancer-specific mortality

2019· review· en· W2918113141 on OpenAlexafffund
Maria Escala-Garcia, Qi Guo, Thilo Dörk, Sander Canisius, Renske Keeman, Joe Dennis, Jonathan Beesley, Julie Lecarpentier, Manjeet K. Bolla, Qin Wang, Jean Abraham, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Paul L. Auer, Matthias W. Beckmann, Sabine Behrens, Javier Benı́tez, Marina Bermisheva, Leslie Bernstein, Carl Blomqvist, Bram Boeckx, Stig E. Bojesen, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Hiltrud Brauch, Hermann Brenner, Adam R. Brentnall, Louise A. Brinton, Per Broberg, Ian W. Brock, Sara Y. Brucker, Barbara Burwinkel, Carlos Caldas, Trinidad Caldés, Daniele Campa, Federico Canzian, Ángel Carracedo, Brian D. Carter, Jose E. Castelao, Jenny Chang‐Claude, Stephen J. Chanock, Georgia Chenevix‐Trench, Ting‐Yuan David Cheng, Suet‐Feung Chin, Christine L. Clarke, Emilie Cordina‐Duverger, Fergus J. Couch, David G. Cox, Angela Cox, Simon S. Cross, Kamila Czene, Mary B. Daly, Peter Devilee, Janet Dunn, Alison M. Dunning, Lorraine Durcan, Miriam Dwek, Helena Earl, Arif B. Ekici, A. Heather Eliassen, Carolina Ellberg, Christoph Engel, Mikael Eriksson, D. Gareth Evans, Jonine D. Figueroa, Dieter Flesch‐Janys, Henrik Flyger, Marike Gabrielson, Manuela Gago-Domínguez, Eva Galle, Susan M. Gapstur, Montserrat García‐Closas, José Á. García-Sáenz, Mia M. Gaudet, Angela George, V. Georgoulias, Graham G. Giles, Gord Glendon, Anna González‐Neira, Grethe I.G. Alnæs, Mervi Grip, Pascal Guénel, Lothar Haeberle, Christopher A. Haiman, Niclas Håkansson, Per Hall, Ute Hamann, Susan E. Hankinson, Elaine F. Harkness, Patricia Harrington, Steven N. Hart, Jaana M. Hartikainen, Alexander Hein, Peter Hillemanns, Louise Hiller, Bernd Holleczek, Antoinette Hollestelle, Maartje J. Hooning, Robert N. Hoover, John L. Hopper, Anthony Howell, Guanmengqian Huang, Keith Humphreys, David J. Hunter, Wolfgang Janni, Esther M. John, Michael E. Jones, Arja Jukkola‐Vuorinen, Audrey Jung, Rudolf Kaaks, Maria Kabisch, Katarzyna Kaczmarek, Michael J. Kerin, Sofia Khan, Э. К. Хуснутдинова, Johanna I. Kiiski, Cari M. Kitahara, Julia A. Knight, Yon‐Dschun Ko, Linetta B. Koppert, Veli‐Matti Kosma, Peter Kraft, Vessela N. Kristensen, Ute Krüger, Tabea Kühl, Diether Lambrechts, Loı̈c Le Marchand, Eunjung Lee, Flavio Lejbkowicz, Lian Li, Annika Lindblom, Sara Lindström, Martha S. Linet, Jolanta Lissowska, Wing‐Yee Lo, Sibylle Loibl, Jan Lubiński, Michael P. Lux, Robert J. MacInnis, Melanie Maierthaler, Tom Maishman, Enes Makalic, Mehdi Manoochehri, Siranoush Manoukian, Sara Margolin, Marı́a Elena Martı́nez, Dimitrios Mavroudis, Catriona McLean, Alfons Meindl, Pooja Middha, Nicola Miller, Roger L. Milne, Fernando Moreno, Anna Marie Mulligan, Claire Mulot, Rami Nassir, Susan L. Neuhausen, Sune F. Nielsen, Børge G. Nordestgaard, Aaron D. Norman, Håkan Olsson, Nick Orr, V. Shane Pankratz, Tjoung‐Won Park‐Simon, José Ignacio Arias Pérez, Clara Pérez-Barrios, Paolo Peterlongo, Christos Petridis, Mila Pinchev, K. Prajzendanc, Ross L. Prentice, Nadège Presneau, Darya Prokofieva, Katri Pylkäs, Brigitte Rack, Paolo Radice, Dhanya Ramachandran, Gad Rennert, Hedy S. Rennert, Valerie Rhenius, Atocha Romero, Rebecca Roylance, Emmanouil Saloustros, Elinor J. Sawyer, Daniel F. Schmidt, Rita K. Schmutzler, Andreas Schneeweiß, Minouk J. Schoemaker, Fredrick R. Schumacher, Lukas Schwentner, Rodney J. Scott, Christopher G. Scott, Caroline Seynaeve, Mitul Shah, Jacques Simard, Ann Smeets, Christof Sohn, Melissa C. Southey, Anthony J. Swerdlow, Aline Talhouk, Rulla M. Tamimi, William Tapper, Manuel R. Teixeira, Maria Tengström, Mary Beth Terry, Kathrin Thöne, Rob A.�E.�M. Tollenaar, Ian Tomlinson, Diana Torres, Thérèse Truong, Constance Turman, Clare Turnbull, Hans-Ulrich Ulmer, Michael Untch, Celine M. Vachon, Christi J. van Asperen, Ans M.W. van den Ouweland, Elke M. van Veen, Camilla Wendt, Alice S. Whittemore, Walter C. Willett, Robert Winqvist, Alicja Wolk, Xiaohong R. Yang, Yan Zhang, Douglas F. Easton, Peter A. Fasching, Heli Nevanlinna, Paul D.P. Pharoah, Marjanka K. Schmidt

Bibliographic record

VenueBritish Journal of Cancer · 2019
Typereview
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBRCA gene mutations in cancer
Canadian institutionsUniversité LavalBC Cancer AgencyCentre hospitalier universitaire de QuébecSinai Health SystemUniversity of British ColumbiaCentre hospitalier de l'Université LavalVancouver General HospitalMount Sinai HospitalLunenfeld-Tanenbaum Research InstitutePublic Health OntarioUniversity Health NetworkUniversity of Toronto
FundersServicio Gallego de SaludProgramme Grants for Applied ResearchBiotieteiden ja Ympäristön Tutkimuksen ToimikuntaInstituto de Salud Carlos IIIMedical Research CouncilImperial Experimental Cancer Medicine CentreNational Institutes of HealthHellenic Health FoundationFreistaat SachsenDeutschen Konsortium für Translationale KrebsforschungXunta de GaliciaRheinische Friedrich-Wilhelms-Universität BonnMutuelle Générale de l'Education NationaleInstitut Gustave-RoussyMinistero dello Sviluppo EconomicoCenters for Disease Control and PreventionInstitut National Du CancerCanadian Institutes of Health ResearchSigrid Juséliuksen SäätiöNational Health and Medical Research CouncilOulun YliopistoDeutsche KrebshilfeKWF KankerbestrijdingVetenskapsrådetStockholms Läns LandstingLigue Contre le CancerKuopion Yliopistollinen SairaalaKarolinska InstitutetOvarian Cancer Research FundBundesministerium für Bildung und ForschungMinisterio de Economía y CompetitividadAir Force Materiel CommandEuropean Regional Development FundKing's College LondonAcademy of FinlandRussian Foundation for Basic ResearchUniversity of CreteInstitut National de la Santé et de la Recherche MédicaleCancer AustraliaAgence Nationale de la RechercheNational Institute on AgingRobert Bosch StiftungUniversity of WestminsterEuropean CommissionCancerfondenNational Cancer InstituteBreast Cancer NowCancer Institute NSWFondation de FranceNIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer ResearchBreast Cancer CampaignEberhard Karls Universität TübingenFondation du cancer du sein du QuébecNational Breast Cancer FoundationAgence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du TravailSwedish Cancer FoundationAgency for Science, Technology and ResearchLon V. Smith FoundationMinistère du Développement Économique, de l’Innovation et de l’ExportationGentofte HospitalDeutsche Gesetzliche UnfallversicherungUniversity of California, IrvineKreftforeningenDavid F. and Margaret T. Grohne Family FoundationCancer Research UKU.S. Department of DefenseNational Heart, Lung, and Blood InstituteItä-Suomen YliopistoGenome CanadaSundhed og Sygdom, Det Frie ForskningsrådCentre International de Recherche sur le CancerDeutsches KrebsforschungszentrumWorld Cancer Research FundHelsingin ja Uudenmaan SairaanhoitopiiriSusan G. Komen for the CureStavros Niarchos FoundationUniversity of Southern CaliforniaAssociazione Italiana per la Ricerca sul CancroBeckman Research Institute, City of HopeCancer Council VictoriaCalifornia Department of Public HealthMinisterio de Sanidad, Servicios Sociales e IgualdadUniversity of CambridgeGovernment of CanadaU.S. Department of Health and Human ServicesAmerican Cancer SocietyBreast Cancer Research FoundationNational Institute for Health and Care ResearchNorges ForskningsrådDivision of Cancer Prevention, National Cancer Institute
KeywordsBreast cancerHazard ratioGermlineOncologyGenome-wide association studyGermline mutationCancerBiologyConfidence intervalInternal medicineDiseaseGeneticsMedicineGeneSingle-nucleotide polymorphismMutationGenotype

Abstract

fetched live from OpenAlex

We examined the associations between germline variants and breast cancer mortality using a large meta-analysis of women of European ancestry. METHODS: Meta-analyses included summary estimates based on Cox models of twelve datasets using ~10.4 million variants for 96,661 women with breast cancer and 7697 events (breast cancer-specific deaths). Oestrogen receptor (ER)-specific analyses were based on 64,171 ER-positive (4116) and 16,172 ER-negative (2125) patients. We evaluated the probability of a signal to be a true positive using the Bayesian false discovery probability (BFDP). RESULTS: We did not find any variant associated with breast cancer-specific mortality at P < 5 10 -8 . For ER-positive disease, the most significantly associated variant was chr7:rs4717568 (BFDP = 7%, P = 1.28 10 -7 , hazard ratio [HR] = 0.88, 95% confidence interval [CI] = 0.84-0.92); the closest gene is AUTS2. For ER-negative disease, the most significant variant was chr7:rs67918676 (BFDP = 11%, P = 1.38 10 -7 , HR = 1.27, 95% CI = 1.16-1.39); located within a long intergenic non-coding RNA gene (AC004009.3), close to the HOXA gene cluster. CONCLUSIONS: We uncovered germline variants on chromosome 7 at BFDP < 15% close to genes for which there is biological evidence related to breast cancer outcome. However, the paucity of variants associated with mortality at genome-wide significance underpins the challenge in providing genetic-based individualised prognostic information for breast cancer patients.

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)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Other design · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.971
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
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 head0.033
GPT teacher head0.344
Teacher spread0.311 · 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.

Study designOther design
Domainnot available
GenreReview

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".

Quick stats

Citations73
Published2019
Admission routes2
Has abstractyes

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