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Record W1964251403 · doi:10.1371/journal.pone.0042380

Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

2012· article· en· W1964251403 on OpenAlexafffund
Rebecca Hein, Melanie Maranian, John L. Hopper, Miroslaw K. Kapuscinski, Melissa C. Southey, Daniel J. Park, Marjanka K. Schmidt, Annegien Broeks, Frans B.L. Hogervorst, H. Bas Bueno-de-Mesquit, Kenneth Muir, Artitaya Lophatananon, Suthee Rattanamongkongul, Puttisak Puttawibul, Peter A. Fasching, Alexander Hein, Arif B. Ekici, Matthias W. Beckmann, Olivia Fletcher, Nichola Johnson, Isabel dos‐Santos‐Silva, Julian Peto, Elinor J. Sawyer, Ian Tomlinson, Michael J. Kerin, Nicola Miller, Frederick Marmee, Andreas Schneeweiß, Christof Sohn, Barbara Burwinkel, Pascal Guénel, Emilie Cordina-Duverger, F. Ménégaux, Thérèse Truong, Stig E. Bojesen, Børge G. Nordestgaard, Henrik Flyger, Roger L. Milne, Jose Ignacio Arias Perez, M. Pilar Zamora, Javier Benítez, Hoda Anton-Culver, Argyrios Ziogas, Leslie Bernstein, Christina A. Clarke, Hermann Brenner, Heiko Müller, Volker Arndt, Christa Stegmaier, Nazneen Rahman, Sheila Seal, Clare Turnbull, Anthony Renwick, Alfons Meindl, Sarah Schott, Claus R. Bartram, Rita K. Schmutzler, Hiltrud Brauch, Ute Hamann, Yon‐Dschun Ko, Shan Wang-Gohrke, Thilo Dörk, Peter Schürmann, Johann H. Karstens, Peter Hillemanns, Heli Nevanlinna, Tuomas Heikkinen, Kristiina Aittomäki, Carl Blomqvist, Natalia Bogdanova, Iosif V. Zalutsky, Natalia Antonenkova, Marina Bermisheva, Darya Prokovieva, Albina Farahtdinova, Э. К. Хуснутдинова, Annika Lindblom, Sara Margolin, Arto Mannermaa, Vesa Kataja, Veli-Matti Kosma, Jaana M. Hartikainen, Xiaoqing Chen, Jonathan Beesley, kConFab Investigators, Diether Lambrechts, Hui Zhao, P. Neven, Hans Wildiers, Stefan Nickels, Dieter Flesch-Janys, Paolo Radice, Paolo Peterlongo, Siranoush Manoukian, Monica Barile, Fergus J. Couch, Janet E. Olson, Xianshu Wang, Zachary Fredericksen, Graham G. Giles, Laura Baglietto, Catriona McLean, Gianluca Severi, Kenneth Offit, Mark E. Robson, Mia M. Gaudet, Joseph Vijai, Grethe Grenaker Alnæs, Vessela N. Kristensen, Anne-Lise Børresen-Dale, Esther M. John, Alexander Miron, Robert Winqvist, Katri Pylkäs, Arja Jukkola‐Vuorinen, Mervi Grip, Irene L. Andrulis, Julia A. Knight, Gord Glendon, Anna Marie Mulligan, Jonine D. Figueroa, Montserrat García‐Closas, Jolanta Lissowska, Mark E. Sherman, Maartje J. Hooning, John W. M. Martens, Caroline Seynaeve, Margriet Collée, Per Hall, Keith Humpreys, Kamila Czene, Jianjun Liu, Angela Cox, Ian W. Brock, Simon S. Cross, Malcolm Reed, Shahana Ahmed, Maya Ghoussaini, Paul DP. Pharoah, Daehee Kang, Keun-Young Yoo, Dong-Young Noh, Anna Jakubowska, Katarzyna Jaworska, Katarzyna Durda, Elżbieta Złowocka, Suleeporn Sangrajrang, Valérie Gaborieau, Paul Brennan, James McKay, Chen‐Yang Shen, Jyh-Cherng Yu, Huan-Ming Hsu, Ming‐Feng Hou, Nick Orr, Minouk J. Schoemaker, Alan Ashworth, Anthony J. Swerdlow, Amy Trentham‐Dietz, Polly A. Newcomb, Linda Titus, Kathleen M. Egan, Georgia Chenevix‐Trench, Antonis C. Antoniou, Manjeet K. Humphreys, Jonathan J. Morrison, Jenny Chang‐Claude, Douglas F. Easton, Alison M. Dunning

Bibliographic record

VenuePLoS ONE · 2012
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBRCA gene mutations in cancer
Canadian institutionsSt. Michael's HospitalMount Sinai HospitalLunenfeld-Tanenbaum Research InstitutePublic Health OntarioUniversity of TorontoCancer Care Ontario
FundersMedical Research and Materiel CommandNational Cancer InstituteCancer Council TasmaniaMedical Research CouncilUniversity of California, IrvineU.S. ArmyNational Institutes of HealthAlleanza Contro il CancroCancer Research UKUniversität UlmBreast Cancer Research TrustRheinische Friedrich-Wilhelms-Universität BonnAgence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du TravailAgence Française de Sécurité Sanitaire de l'Environnement et du TravailFondazione Italiana per la Ricerca sul CancroInstitut National Du CancerNational Health and Medical Research CouncilOulun YliopistoDeutsche KrebshilfeMedizinischen Hochschule HannoverNorges ForskningsrådAcademia SinicaKuopion Yliopistollinen SairaalaDeutsche ForschungsgemeinschaftDeutsche Gesetzliche UnfallversicherungInstitute of Biomedical Sciences, Academia SinicaMinistero della SaluteAgence Nationale de la RechercheBundesministerium für Bildung und ForschungNational Breast Cancer FoundationAgency for Science, Technology and ResearchAcademy of FinlandKing's College LondonWellcome TrustMemorial Sloan-Kettering Cancer CenterCancerfondenFondation de FranceBreast Cancer CampaignNational Institute for Health and Care ResearchAssociazione Italiana per la Ricerca sul CancroItä-Suomen YliopistoLon V. Smith FoundationKWF KankerbestrijdingHerlev HospitalU.S. Department of Health and Human ServicesMayo ClinicSundhed og Sygdom, Det Frie ForskningsrådCentre International de Recherche sur le CancerLigue Contre le CancerDeutsches KrebsforschungszentrumCancer Council VictoriaCalifornia Department of Public HealthHelsingin ja Uudenmaan SairaanhoitopiiriSusan G. Komen for the CureTaiwan BiobankEuropean CommissionBreast Cancer Research FoundationCancer Care Ontario
KeywordsSingle-nucleotide polymorphismGenome-wide association studyBreast cancerOdds ratioSNPOncologyInternal medicineEstrogen receptorMedicineGenetic associationGeneticsBiologyCancerGenotypeGene

Abstract

fetched live from OpenAlex

The 6q25.1 locus was first identified via a genome-wide association study (GWAS) in Chinese women and marked by single nucleotide polymorphism (SNP) rs2046210, approximately 180 Kb upstream of ESR1. There have been conflicting reports about the association of this locus with breast cancer in Europeans, and a GWAS in Europeans identified a different SNP, tagged here by rs12662670. We examined the associations of both SNPs in up to 61,689 cases and 58,822 controls from forty-four studies collaborating in the Breast Cancer Association Consortium, of which four studies were of Asian and 39 of European descent. Logistic regression was used to estimate odds ratios (OR) and 95% confidence intervals (CI). Case-only analyses were used to compare SNP effects in Estrogen Receptor positive (ER+) versus negative (ER-) tumours. Models including both SNPs were fitted to investigate whether the SNP effects were independent. Both SNPs are significantly associated with breast cancer risk in both ethnic groups. Per-allele ORs are higher in Asian than in European studies [rs2046210: OR (A/G) = 1.36 (95% CI 1.26-1.48), p = 7.6 × 10(-14) in Asians and 1.09 (95% CI 1.07-1.11), p = 6.8 × 10(-18) in Europeans. rs12662670: OR (G/T) = 1.29 (95% CI 1.19-1.41), p = 1.2 × 10(-9) in Asians and 1.12 (95% CI 1.08-1.17), p = 3.8 × 10(-9) in Europeans]. SNP rs2046210 is associated with a significantly greater risk of ER- than ER+ tumours in Europeans [OR (ER-) = 1.20 (95% CI 1.15-1.25), p = 1.8 × 10(-17) versus OR (ER+) = 1.07 (95% CI 1.04-1.1), p = 1.3 × 10(-7), p(heterogeneity) = 5.1 × 10(-6)]. In these Asian studies, by contrast, there is no clear evidence of a differential association by tumour receptor status. Each SNP is associated with risk after adjustment for the other SNP. These results suggest the presence of two variants at 6q25.1 each independently associated with breast cancer risk in Asians and in Europeans. Of these two, the one tagged by rs2046210 is associated with a greater risk of ER- tumours.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.011
metaresearch head score (Gemma)0.021
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.011
Threshold uncertainty score0.059

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0110.021
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0020.002
Bibliometrics0.0040.005
Science and technology studies0.0010.001
Scholarly communication0.0020.001
Open science0.0010.002
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0070.001

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 head0.051
GPT teacher head0.312
Teacher spread0.261 · 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 source (direct Gemma or distilled Codex), 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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Citations54
Published2012
Admission routes2
Has abstractyes

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Same venuePLoS ONESame topicBRCA gene mutations in cancerFrench-language works237,207