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Record W7162005381 · doi:10.82308/42154

Analyzing the genetic landscape of French-Canadian hereditary breast cancer women that carry pathogenic BRCA1 or BRCA2 variants

2021· dissertation· en· W7162005381 on OpenAlexaboutno aff
Neil Recio

Bibliographic record

Venuenot available
Typedissertation
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBRCA gene mutations in cancer
Canadian institutionsnot available
Fundersnot available
KeywordsPALB2MUTYHCHEK2GeneExome sequencingHomologous recombinationCancerExomeBreast cancer

Abstract

fetched live from OpenAlex

Family history of breast cancer (BC) is a factor that increases an individual’s risk for BC owing to the transmission of disease-causing alleles. Pathogenic variants in BRCA1 and BRCA2 are commonly found in women that are at a high-risk of developing BC and confer estimated lifetime risks ranging between 65-79% and 61-77%, respectively. Similar to many other BC predisposing genes (BCPGs) such as ATM, CHEK2 and PALB2, BRCA1/BRCA2 play an important role in the maintenance of genomic integrity through their involvement in the homologous recombination pathway. While pathogenic variants in BRCA1/BRCA2 are found at a frequency of less than 1/40 people in the general population, founder populations, such as the French-Canadians (FC) of Quebec, have an enrichment of pathogenic variants in BRCA1/BRCA2 due to common ancestry. Our lab identified two hereditary BC (HBC) cases that harbour pathogenic variants in two BCPGs, which I refer to as a genetic collision event. The biological implications of this phenomenon are unknown due to the paucity of cases that have been reported. Given the role of known BCPGs in DNA repair pathways, I performed bioinformatic analyses on whole exome sequencing data from 58 FC HBC cases that harbour pathogenic variants in BRCA1/BRCA2 to determine whether they harbour pathogenic variants in other genes involved in DNA repair pathways. I have identified eight candidate variants in ATM, BARD1, CHEK2, ERCC6, MLH1, MUTYH and NSMCE2. I screened these candidate variants in other FC study groups consisting of HBC cases, regardless of BRCA1/BRCA2-carrier status, and cancer-free individuals and identified additional carriers in two cancer-free males (2/119, 1.7%) and one cancer-free female (1/52, 1.9%). To better elucidate the effects of genetic collision events, I reviewed the published peer reviewed literature for other BC cases in which genetic collision events can be observed and compared their clinical features with single variant BC cases from our FC study groups. I found that a significantly higher frequency of double variant BC cases developed multiple primary tumours in comparison to single variant BC cases. Therefore, these findings demonstrate that FC HBC cases that harbour pathogenic variants in BRCA1/BRCA2 also carry co-occurring pathogenic variants in other DNA repair pathway genes that may influence disease characteristics

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)0.000
metaresearch head score (Gemma)0.001
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 score0.175
Threshold uncertainty score0.351

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0020.003
Science and technology studies0.0020.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0030.000

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 head0.009
GPT teacher head0.250
Teacher spread0.241 · 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".

Quick stats

Citations0
Published2021
Admission routes1
Has abstractyes

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