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Record W6963156640 · doi:10.17863/cam.56822

Two truncating variants in FANCC and breast cancer risk

2019· article· en· W6963156640 on OpenAlexfundno aff

Bibliographic record

VenueApollo (University of Cambridge) · 2019
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicDNA Repair Mechanisms
Canadian institutionsnot available
FundersServicio Gallego de SaludInstituto de Salud Carlos IIICancer Council Western AustraliaCancer Council VictoriaWorld Cancer Research FundMedical Research CouncilManchester Biomedical Research CentreCenter for Agroforestry, University of MissouriUniversity of California, IrvineHellenic Health FoundationFreistaat SachsenBiomedical Research CouncilFederal Agency for Scientific OrganizationsDeutschen Konsortium für Translationale KrebsforschungUniversitätsklinikum Hamburg-EppendorfDr. Ralph and Marian Falk Medical Research TrustXunta de GaliciaMutuelle Générale de l'Education NationaleImperial Experimental Cancer Medicine CentreInstitut Gustave-RoussyMinistero dello Sviluppo EconomicoMemorial Sloan-Kettering Cancer CenterCentre International de Recherche sur le CancerKreftforeningenInstitut National Du CancerNational Health and Medical Research CouncilMinistry of Education, Science and TechnologyAcademia SinicaDeutsche KrebshilfeCancer Institute NSWMedizinischen Hochschule HannoverInstituto Mexicano del Seguro SocialKWF KankerbestrijdingVetenskapsrådetNational Medical Research CouncilNorges ForskningsrådStockholms Läns LandstingUniversity of WestminsterLigue Contre le CancerAssociazione Italiana per la Ricerca sul CancroKarolinska InstitutetUniversity of Southern CaliforniaAlexander von Humboldt-StiftungCancerfondenItä-Suomen YliopistoEberhard Karls Universität TübingenAmerican Cancer SocietyRussian Foundation for Basic ResearchKuopion Yliopistollinen SairaalaUniversity of CreteInstitut National de la Santé et de la Recherche MédicaleAgence Nationale de la RechercheJapan Agency for Medical Research and DevelopmentDeutsche Gesetzliche UnfallversicherungGentofte HospitalDeutsche ForschungsgemeinschaftAgency for Science, Technology and ResearchCanadian Institutes of Health ResearchEuropean CommissionUniversity College LondonKerry Group Kuok FoundationStavros Niarchos FoundationFondation de FranceNational Research FoundationNIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer ResearchBreast Cancer CampaignNational Cancer InstituteEuropean Regional Development FundMinisterio de Sanidad, Servicios Sociales e IgualdadUniversity of CambridgeGovernment of CanadaNational Breast Cancer FoundationAgence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du TravailNational Institute of Environmental Health SciencesSwedish Cancer FoundationLon V. Smith FoundationMinistère du Développement Économique, de l’Innovation et de l’ExportationKorea Health Industry Development InstituteClaremont Graduate UniversityMcGill University Health CentreInstitute of Biomedical Sciences, Academia SinicaDavid F. and Margaret T. Grohne Family FoundationConsejo Nacional de Ciencia y TecnologíaSundhed og Sygdom, Det Frie ForskningsrådDeutsches KrebsforschungszentrumBreast Cancer Research FoundationMcGill UniversityHelsingin ja Uudenmaan SairaanhoitopiiriUniversité LavalNational Research Foundation of KoreaCalifornia Department of Public HealthGenome CanadaCentre Hospitalier Universitaire de QuébecRheinische Friedrich-Wilhelms-Universität BonnAvon Foundation for WomenOak FoundationBreast Cancer Research TrustFondation du cancer du sein du QuébecDeutscher Akademischer AustauschdienstMinistry of Public HealthYayasan Sime DarbyInstituto de Seguriidad y Servicios Sociales de los Trabadores del EstadoFonds Wetenschappelijk OnderzoekCenters for Disease Control and PreventionNational Institute for Health and Care ResearchOhio State UniversitySusan G. Komen for the CureTaiwan BiobankProgramme Grants for Applied ResearchRobert Bosch StiftungU.S. Department of Health and Human ServicesMinisterio de Economía y CompetitividadBundesministerium für Bildung und ForschungBeckman Research Institute, City of HopeMinistry of Education, Culture, Sports, Science and TechnologyOvarian Cancer Research FundNational Institutes of HealthDivision of Cancer Prevention, National Cancer InstituteCancer Research UK
KeywordsPALB2Fanconi anemiaBreast cancerGenotypeGeneBRCA2 ProteinCancer

Abstract

fetched live from OpenAlex

Abstract: Fanconi anemia (FA) is a genetically heterogeneous disorder with 22 disease-causing genes reported to date. In some FA genes, monoallelic mutations have been found to be associated with breast cancer risk, while the risk associations of others remain unknown. The gene for FA type C, FANCC, has been proposed as a breast cancer susceptibility gene based on epidemiological and sequencing studies. We used the Oncoarray project to genotype two truncating FANCC variants (p.R185X and p.R548X) in 64,760 breast cancer cases and 49,793 controls of European descent. FANCC mutations were observed in 25 cases (14 with p.R185X, 11 with p.R548X) and 26 controls (18 with p.R185X, 8 with p.R548X). There was no evidence of an association with the risk of breast cancer, neither overall (odds ratio 0.77, 95%CI 0.44–1.33, p = 0.4) nor by histology, hormone receptor status, age or family history. We conclude that the breast cancer risk association of these two FANCC variants, if any, is much smaller than for BRCA1, BRCA2 or PALB2 mutations. If this applies to all truncating variants in FANCC it would suggest there are differences between FA genes in their roles on breast cancer risk and demonstrates the merit of large consortia for clarifying risk associations of rare variants.

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 score0.713
Threshold uncertainty score0.501

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 head0.004
GPT teacher head0.197
Teacher spread0.194 · 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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Citations0
Published2019
Admission routes1
Has abstractyes

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