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A noncoding single-nucleotide polymorphism at 8q24 drives <i>IDH1</i> -mutant glioma formation

2022· article· en· 69 citations· W4302425337 on OpenAlex· 10.1126/science.abj2890

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

Full frame distilled prediction

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.

Candidate categories
none
Consensus categories
none
Domain
Candidate signal: noneConsensus signal: none
Study design
Candidate signal: Bench or experimentalConsensus signal: Bench or experimental
Genre
Candidate signal: EmpiricalConsensus signal: Empirical
Teacher disagreement score
0.020
Threshold uncertainty score
0.707
Validation status
machine_predicted_unvalidated · codex-gemma-dda1882f352a

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

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.

Opus teacher head0.022
GPT teacher head0.257
Teacher spread
0.235 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

Establishing causal links between inherited polymorphisms and cancer risk is challenging. Here, we focus on the single-nucleotide polymorphism rs55705857, which confers a sixfold greater risk of isocitrate dehydrogenase ( IDH) –mutant low-grade glioma (LGG). We reveal that rs55705857 itself is the causal variant and is associated with molecular pathways that drive LGG. Mechanistically, we show that rs55705857 resides within a brain-specific enhancer, where the risk allele disrupts OCT2/4 binding, allowing increased interaction with the Myc promoter and increased Myc expression. Mutating the orthologous mouse rs55705857 locus accelerated tumor development in an Idh1 R132H -driven LGG mouse model from 472 to 172 days and increased penetrance from 30% to 75%. Our work reveals mechanisms of the heritable predisposition to lethal glioma in ~40% of LGG patients.

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.

The record

Venue
Science
Topic
Glioma Diagnosis and Treatment
Field
Medicine
Canadian institutions
Ontario Institute for Cancer ResearchPrincess Margaret Cancer CentreUniversity of TorontoUniversity Health NetworkHospital for Sick ChildrenLunenfeld-Tanenbaum Research InstituteMount Sinai Hospital
Funders
Lawrence Berkeley National LaboratoryNational Institute of Neurological Disorders and StrokeNational Institute of General Medical SciencesCenter for Individualized Medicine, Mayo ClinicNational Cancer InstituteNational Institutes of HealthCancer Research UKGovernment of OntarioNational Human Genome Research InstituteUniversity of California, San FranciscoU.S. Department of Energy
Keywords
PenetranceIsocitrate dehydrogenaseIDH1Locus (genetics)BiologySingle-nucleotide polymorphismGliomaAlleleMutantGeneticsEnhancerNucleotideGeneCancer researchPhenotypeTranscription factorGenotypeEnzymeBiochemistry
Has abstract in OpenAlex
yes