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Record W2952969165 · doi:10.1002/ijc.32516

DNA repair and cancer in colon and rectum: Novel players in genetic susceptibility

2019· article· en· W2952969165 on OpenAlexaff
Barbara Pardini, Alda Corrado, Elisa Paolicchi, Giovanni Cugliari, Sonja I. Berndt, Stéphane Bezieau, Stephanie A. Bien, Hermann Brenner, Bette J. Caan, Peter T. Campbell, Graham Casey, Andrew T. Chan, Jenny Chang‐Claude, Michelle Cotterchio, Manish Gala, Steven Gallinger, Robert W. Haile, Tabitha A. Harrison, Richard B. Hayes, Michael Hoffmeister, John L. Hopper, Li Hsu, Jeroen R. Huyghe, Mark A. Jenkins, Loı̈c Le Marchand, Yi Lin, Noralane M. Lindor, Hongmei Nan, Polly A. Newcomb, Shuji Ogino, John D. Potter, Robert E. Schoen, Martha L. Slattery, Emily White, Ludmila Vodičková, Veronika Vymetálková, Pavel Vodička, Federica Gemignani, Ulrike Peters, Alessio Naccarati, Stefano Landi

Bibliographic record

VenueInternational Journal of Cancer · 2019
Typearticle
Languageen
FieldMedicine
TopicGenetic factors in colorectal cancer
Canadian institutionsMount Sinai HospitalCancer Care Ontario
FundersNational Human Genome Research InstituteNational Heart, Lung, and Blood InstituteNational Institute on AgingNational Cancer InstituteNational Institutes of HealthConseil Régional des Pays de la LoireCalifornia Department of Public HealthAssociation Anne de Bretagne GenetiqueMinisterstvo Zdravotnictví Ceské RepublikyGrantová Agentura České RepublikyFondazione Umberto Veronesi
KeywordsColorectal cancerMLH1Single-nucleotide polymorphismCancerRectumDNA mismatch repairDNA repairCarcinogenesisGeneticsBiologyOncologyMedicineInternal medicineCancer researchGeneGenotype

Abstract

fetched live from OpenAlex

Interindividual differences in DNA repair systems may play a role in modulating the individual risk of developing colorectal cancer. To better ascertain the role of DNA repair gene polymorphisms on colon and rectal cancer risk individually, we evaluated 15,419 single nucleotide polymorphisms (SNPs) within 185 DNA repair genes using GWAS data from the Colon Cancer Family Registry (CCFR) and the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO), which included 8,178 colon cancer, 2,936 rectum cancer cases and 14,659 controls. Rs1800734 (in MLH1 gene) was associated with colon cancer risk ( p ‐value = 3.5 × 10 −6 ) and rs2189517 (in RAD51B ) with rectal cancer risk ( p ‐value = 5.7 × 10 −6 ). The results had statistical significance close to the Bonferroni corrected p ‐value of 5.8 × 10 −6 . Ninety‐four SNPs were significantly associated with colorectal cancer risk after Binomial Sequential Goodness of Fit (BSGoF) procedure and confirmed the relevance of DNA mismatch repair (MMR) and homologous recombination pathways for colon and rectum cancer, respectively. Defects in MMR genes are known to be crucial for familial form of colorectal cancer but our findings suggest that specific genetic variations in MLH1 are important also in the individual predisposition to sporadic colon cancer. Other SNPs associated with the risk of colon cancer (e.g., rs16906252 in MGMT ) were found to affect mRNA expression levels in colon transverse and therefore working as possible cis‐eQTL suggesting possible mechanisms of carcinogenesis.

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: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.053
Threshold uncertainty score0.638

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)0.0010.000

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 head0.013
GPT teacher head0.324
Teacher spread0.310 · 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".

Quick stats

Citations50
Published2019
Admission routes1
Has abstractyes

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