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Record W2551180170 · doi:10.1038/srep36874

rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk

2016· article· en· W2551180170 on OpenAlexafffund
Jingjing Liu, Ivona Lončar, J. Margriet Collée, Manjeet K. Bolla, Joe Dennis, Kyriaki Michailidou, Irene L. Andrulis, Monica Barile, Matthias W. Beckmann, Sabine Behrens, Javier Benı́tez, Carl Blomqvist, Bram Boeckx, Natalia Bogdanova, Stig E. Bojesen, Hiltrud Brauch, Paul Brennan, Hermann Brenner, Annegien Broeks, Barbara Burwinkel, Jenny Chang‐Claude, Shou‐Tung Chen, Georgia Chenevix‐Trench, Ching‐Yu Cheng, Ji‐Yeob Choi, Fergus J. Couch, Angela Cox, Simon S. Cross, Katarina Ćuk, Kamila Czene, Thilo Dörk, Isabel dos‐Santos‐Silva, Peter A. Fasching, Jonine D. Figueroa, Henrik Flyger, Montserrat García‐Closas, Graham G. Giles, Gord Glendon, Mark S. Goldberg, Anna González‐Neira, Pascal Guénel, Christopher A. Haiman, Ute Hamann, Steven N. Hart, Mikael Hartman, Sigrid Hatse, John L. Hopper, Hidemi Ito, Anna Jakubowska, Maria Kabisch, Daehee Kang, Veli‐Matti Kosma, Vessela N. Kristensen, Loı̈c Le Marchand, Eunjung Lee, Jingmei Li, Artitaya Lophatananon, Jan Lubiński, Keitaro Matsuo, Roger L. Milne, Kristine Kleivi Sahlberg, Lars Ottestad, Rolf Kåresen, Anita Langerød, Ellen Schlichting, Marit Muri Holmen, Toril Sauer, Vilde Drageset Haakensen, Olav Engebråten, Bjørn Naume, Cecile E. Kiserud, Kristin V. Reinertsen, Åslaug Helland, Margit Riis, Ida Bukholm, Per Eystein Lønning, Anne‐Lise Børresen‐Dale, Grethe I.G. Alnæs, Susan L. Neuhausen, Heli Nevanlinna, Nick Orr, José Ignacio Arias Pérez, Julian Peto, Thomas Choudary Putti, Katri Pylkäs, Paolo Radice, Suleeporn Sangrajrang, Elinor J. Sawyer, Marjanka K. Schmidt, Andreas Schneeweiß, Chen‐Yang Shen, Martha J. Shrubsole, Xiao‐Ou Shu, Jacques Simard, Melissa C. Southey, Anthony J. Swerdlow, Soo‐Hwang Teo, Daniel C. Tessier, Somchai Thanasitthichai, Ian Tomlinson, Diana Torres, Thérèse Truong, Chiu-Chen Tseng, Celine M. Vachon, Robert Winqvist, Anna H. Wu, Drakoulis Yannoukakos, Wei Zheng, Per Hall, Alison M. Dunning, Douglas F. Easton, Maartje J. Hooning, Ans M.W. van den Ouweland, John W.M. Martens, Antoinette Hollestelle

Bibliographic record

VenueScientific Reports · 2016
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicRNA modifications and cancer
Canadian institutionsMcGill University and Génome Québec Innovation CentreUniversité LavalCentre hospitalier universitaire de QuébecMcGill UniversityUniversity of TorontoRoyal Victoria HospitalLunenfeld-Tanenbaum Research InstituteMount Sinai Hospital
FundersMedical Research and Materiel CommandMedisinske fakultet, Universitetet i OsloInstitute of Biomedical Sciences, Academia SinicaUniversitätsklinikum Hamburg-EppendorfNIHR Oxford Biomedical Research CentreBiomedical Research CouncilNational Health and Medical Research CouncilMedical Research CouncilCenter for Agroforestry, University of MissouriHorizon 2020 Framework ProgrammeU.S. ArmyNational Institutes of HealthDeutschen Konsortium für Translationale KrebsforschungAgence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du TravailFondazione Italiana per la Ricerca sul CancroInstitut National Du CancerDeutsche KrebshilfeMedizinischen Hochschule HannoverKWF KankerbestrijdingNational Research Foundation of KoreaCanadian Institutes of Health ResearchGeneral Secretariat for Research and TechnologyChina Scholarship CouncilMinistry of Education, Science and TechnologyOvarian Cancer Research FundMinistry of Education, Culture, Sports, Science and TechnologyBundesministerium für Bildung und ForschungMinisterio de Economía y CompetitividadCancer AustraliaAgence Nationale de la RechercheRobert Bosch StiftungDeutsches KrebsforschungszentrumHøgskolen i Oslo og AkershusEuropean Social FundAgency for Science, Technology and ResearchCancer Council South AustraliaFonds Wetenschappelijk OnderzoekNational Cancer InstituteCancer Institute NSWNational Breast Cancer FoundationEuropean CommissionNational Medical Research CouncilEberhard Karls Universität TübingenRheinische Friedrich-Wilhelms-Universität BonnBreast Cancer Research TrustNederlandse Organisatie voor Wetenschappelijk OnderzoekDeutsche Gesetzliche UnfallversicherungGentofte HospitalKuopion Yliopistollinen SairaalaAcademia SinicaNational Research FoundationNational Institute for Health and Care ResearchNorges Teknisk-Naturvitenskapelige UniversitetMcGill University Health CentreUniversity of California, IrvineDavid F. and Margaret T. Grohne Family FoundationGénome QuébecBreast Cancer Research FoundationMcGill UniversityJapan Agency for Medical Research and DevelopmentFondation de FranceCalifornia Breast Cancer Research ProgramNIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer ResearchHelsingin ja Uudenmaan SairaanhoitopiiriCancer Council VictoriaCalifornia Department of Public HealthUniversitetet i OsloSundhed og Sygdom, Det Frie ForskningsrådLon V. Smith FoundationItä-Suomen YliopistoCancer Council NSWSusan G. Komen for the CureTaiwan BiobankCancer Research UKAssociazione Italiana per la Ricerca sul CancroMinistry of Public HealthBeckman Research Institute, City of HopeCancer Council TasmaniaWorld Health OrganizationUniversity of Southern CaliforniaInternational Business Machines CorporationUniversity of CambridgeKing's College LondonUniversitetet i TromsøU.S. Department of Health and Human Services
KeywordsBreast cancerGenotypeOncologyMedicineInternal medicineColorectal cancerMenarcheCancerCase-control studyMenopauseBiologyGeneticsGene

Abstract

fetched live from OpenAlex

Abstract NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs2735383 G > C, located in a microRNA binding site in the 3′-untranslated region (UTR) of NBS1, was shown to be associated with increased susceptibility to lung and colorectal cancer. However, the relation between rs2735383 and susceptibility to breast cancer is not yet clear. Therefore, we genotyped rs2735383 in 1,170 familial non-BRCA1/2 breast cancer cases and 1,077 controls using PCR-based restriction fragment length polymorphism (RFLP-PCR) analysis, but found no association between rs2735383CC and breast cancer risk (OR = 1.214, 95% CI = 0.936–1.574, P = 0.144). Because we could not exclude a small effect size due to a limited sample size, we further analyzed imputed rs2735383 genotypes (r2 > 0.999) of 47,640 breast cancer cases and 46,656 controls from the Breast Cancer Association Consortium (BCAC). However, rs2735383CC was not associated with overall breast cancer risk in European (OR = 1.014, 95% CI = 0.969–1.060, P = 0.556) nor in Asian women (OR = 0.998, 95% CI = 0.905–1.100, P = 0.961). Subgroup analyses by age, age at menarche, age at menopause, menopausal status, number of pregnancies, breast feeding, family history and receptor status also did not reveal a significant association. This study therefore does not support the involvement of the genotype at NBS1 rs2735383 in breast cancer susceptibility.

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)0.001
metaresearch head score (Gemma)0.002
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 score0.006
Threshold uncertainty score0.019

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0060.001

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 head0.010
GPT teacher head0.237
Teacher spread0.227 · 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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Citations4
Published2016
Admission routes2
Has abstractyes

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