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Record W2070999406 · doi:10.1093/carcin/bgu326

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

2015· article· en· W2070999406 on OpenAlexafffund
Maria Kabisch, Justo Lorenzo Bermejo, Thomas Dünnebier, Shibo Ying, Kyriaki Michailidou, Manjeet K. Bolla, Qin Wang, Joe Dennis, Mitul Shah, Barbara Perkins, Kamila Czene, Hatef Darabi, Mikael Eriksson, Stig E. Bojesen, Børge G. Nordestgaard, Sune F. Nielsen, Henrik Flyger, Diether Lambrechts, Patrick Neven, Stéphanie Peeters, Caroline Weltens, Fergus J. Couch, Janet E. Olson, Xianshu Wang, Kristen S. Purrington, Jenny Chang‐Claude, Anja Rudolph, Petra Seibold, Dieter Flesch‐Janys, Julian Peto, Isabel dos‐Santos‐Silva, Nichola Johnson, Olivia Fletcher, Heli Nevanlinna, Taru Muranen, Kristiina Aittomäki, Carl Blomqvist, Marjanka K. Schmidt, Annegien Broeks, Sten Cornelissen, Frans B.L. Hogervorst, Jingmei Li, Judith S. Brand, Keith Humphreys, Pascal Guénel, Thérèse Truong, F. Ménégaux, Barbara Burwinkel, Frederik Marmé, Rongxi Yang, Peter Bugert, Anna González‐Neira, Javier Benı́tez, M. Pilar Zamora, José Ignacio Arias Pérez, Angela Cox, Simon S. Cross, Malcolm Reed, Irene L. Andrulis, Julia A. Knight, Gord Glendon, Sandrine Tchatchou, Elinor J. Sawyer, Ian Tomlinson, Michael J. Kerin, Nicola Miller, Christopher A. Haiman, Fredrick R. Schumacher, Brian E. Henderson, Loı̈c Le Marchand, Annika Lindblom, Sara Margolin, Maartje J. Hooning, Antoinette Hollestelle, Mieke Kriege, Linetta B. Koppert, John L. Hopper, Melissa C. Southey, Helen Tsimiklis, Carmel Apicella, Seth W. Slettedahl, Amanda E. Toland, Celine M. Vachon, Drakoulis Yannoukakos, Graham G. Giles, Roger L. Milne, Catriona McLean, Peter A. Fasching, Matthias Ruebner, Arif B. Ekici, Matthias W. Beckmann, Hermann Brenner, Aida Karina Dieffenbach, Volker Arndt, Christa Stegmaier, Alan Ashworth, Minouk J. Schoemaker, Anthony J. Swerdlow, Montserrat García‐Closas, Jonine D. Figueroa, Stephen J. Chanock, Jolanta Lissowska, Mark S. Goldberg, France Labrèche, Martine Dumont, Robert Winqvist, Katri Pylkäs, Arja Jukkola‐Vuorinen, Mervi Grip, Hiltrud Brauch, Thomas Brüning, Yon‐Dschun Ko, Paolo Radice, Paolo Peterlongo, Giulietta Scuvera, Stefano Fortuzzi, Natalia Bogdanova, Thilo Dörk, Arto Mannermaa, Vesa Kataja, Veli‐Matti Kosma, Jaana M. Hartikainen, Peter Devilee, Robert A.E.M. Tollenaar, Caroline Seynaeve, Christi J. van Asperen, Anna Jakubowska, Jan Lubiński, Katarzyna Jaworska–Bieniek, Katarzyna Durda, Wei Zheng, Martha J. Shrubsole, Qiuyin Cai, Diana Torres, Hoda Anton‐Culver, Vessela N. Kristensen, François Bacot, Daniel C. Tessier, Daniel Vincent, Craig Luccarini, Caroline Baynes, Shahana Ahmed, Mel Maranian, Jacques Simard, Georgia Chenevix‐Trench, Per Hall, Paul D.P. Pharoah, Alison M. Dunning, Douglas F. Easton, Ute Hamann

Bibliographic record

VenueCarcinogenesis · 2015
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenomics and Chromatin Dynamics
Canadian institutionsMcGill University and Génome Québec Innovation CentreUniversité LavalRoyal Victoria HospitalCentre hospitalier universitaire de QuébecSante MontrealMcGill UniversityMcGill University Health CentreUniversité de MontréalRoyal Victoria Regional Health CentreMount Sinai HospitalLunenfeld-Tanenbaum Research InstitutePublic Health OntarioUniversity of Toronto
FundersNational Cancer InstituteUniversitätsklinikum Hamburg-EppendorfInstituto de Salud Carlos IIIMedical Research CouncilNational Institutes of HealthAkershus UniversitetssykehusRheinische Friedrich-Wilhelms-Universität BonnMinistero dello Sviluppo EconomicoAgence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du TravailNational Health and Medical Research CouncilOulun YliopistoDeutsche KrebshilfeMedizinischen Hochschule HannoverNorges ForskningsrådInstitut National Du CancerLeids Universitair Medisch CentrumUniversitetet i BergenStockholms Läns LandstingKuopion Yliopistollinen SairaalaKarolinska InstitutetCanadian Institutes of Health ResearchGeneral Secretariat for Research and TechnologyOvarian Cancer Research FundBundesministerium für Bildung und ForschungMinisterio de Economía y CompetitividadDeutsche Gesetzliche UnfallversicherungNederlandse Organisatie voor Wetenschappelijk OnderzoekFonds Wetenschappelijk OnderzoekCancerfondenCancer AustraliaAgence Nationale de la RechercheRobert Bosch StiftungNational Breast Cancer FoundationEuropean CommissionHerlev HospitalUniversity of Southern CaliforniaAssociazione Italiana per la Ricerca sul CancroBeckman Research Institute, City of HopeCancer Research UKEberhard Karls Universität TübingenFondation du cancer du sein du QuébecKing's College LondonAcademy of FinlandGénome QuébecNational Institute for Health and Care ResearchItä-Suomen YliopistoMinistère du Développement Économique, de l’Innovation et de l’ExportationLon V. Smith FoundationEuropean Social FundAgency for Science, Technology and ResearchFrancis Crick InstituteMcGill University Health CentreUniversity of California, IrvineDavid F. and Margaret T. Grohne Family FoundationMedisinske fakultet, Universitetet i OsloLigue Contre le CancerDeutsches KrebsforschungszentrumBreast Cancer Research FoundationMcGill UniversityHelsingin ja Uudenmaan SairaanhoitopiiriSusan G. Komen for the CureNIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer ResearchFondation de FranceUniversitetet i OsloSundhed og Sygdom, Det Frie ForskningsrådCancer Council VictoriaCalifornia Department of Public HealthHaukeland UniversitetssjukehusU.S. Department of Health and Human ServicesUniversitetet i TromsøUniversity of Cambridge
KeywordsSingle-nucleotide polymorphismBreast cancerGeneticsBiologyAlleleOdds ratioEstrogen receptorOncologySNPCancerGenotypeInternal medicineMedicineGene

Abstract

fetched live from OpenAlex

The chromosomal passenger complex (CPC) plays a pivotal role in the regulation of cell division. Therefore, inherited CPC variability could influence tumor development. The present candidate gene approach investigates the relationship between single nucleotide polymorphisms (SNPs) in genes encoding key CPC components and breast cancer risk. Fifteen SNPs in four CPC genes (INCENP, AURKB, BIRC5 and CDCA8) were genotyped in 88 911 European women from 39 case-control studies of the Breast Cancer Association Consortium. Possible associations were investigated in fixed-effects meta-analyses. The synonymous SNP rs1675126 in exon 7 of INCENP was associated with overall breast cancer risk [per A allele odds ratio (OR) 0.95, 95% confidence interval (CI) 0.92-0.98, P = 0.007] and particularly with estrogen receptor (ER)-negative breast tumors (per A allele OR 0.89, 95% CI 0.83-0.95, P = 0.0005). SNPs not directly genotyped were imputed based on 1000 Genomes. The SNPs rs1047739 in the 3' untranslated region and rs144045115 downstream of INCENP showed the strongest association signals for overall (per T allele OR 1.03, 95% CI 1.00-1.06, P = 0.0009) and ER-negative breast cancer risk (per A allele OR 1.06, 95% CI 1.02-1.10, P = 0.0002). Two genotyped SNPs in BIRC5 were associated with familial breast cancer risk (top SNP rs2071214: per G allele OR 1.12, 95% CI 1.04-1.21, P = 0.002). The data suggest that INCENP in the CPC pathway contributes to ER-negative breast cancer susceptibility in the European population. In spite of a modest contribution of CPC-inherited variants to the total burden of sporadic and familial breast cancer, their potential as novel targets for breast cancer treatment should be further investigated.

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: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.740
Threshold uncertainty score0.380

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 science0.0010.000
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 head0.019
GPT teacher head0.243
Teacher spread0.224 · 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 designBench or experimental
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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Citations20
Published2015
Admission routes2
Has abstractyes

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