Evidence map›Paper›PMID 24729269›Full record

ArticleFamilial cancer2014

BRCA1 point mutations in premenopausal breast cancer patients from Central Sudan.

Ida Biunno, Gitana Aceto, Khalid Dafaallah Awadelkarim, Annalisa Morgano, Ahmed Elhaj, Elgaylani Abdalla Eltayeb, Dafalla Omer Abuidris, Nasr Eldin Elwali, Chiara Spinelli, Pasquale De Blasio and 2 more

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Article in Familial cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Genetics of breast cancer in African populations: a literature review.Global health, epidemiology and genomics · 2018
    Review
  9. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Ida BiunnoInstitute for Genetic and Biomedical Research, National Research Council, Via Fantoli 16/15, 20138, Milan, Italy.
Gitana Aceto
Khalid Dafaallah Awadelkarim
Annalisa Morgano
Ahmed Elhaj
Elgaylani Abdalla Eltayeb
Dafalla Omer Abuidris
Nasr Eldin Elwali
Chiara Spinelli
Pasquale De Blasio
Ermanna Rovida
Renato Mariani-Costantini
University of Gezira · SDUniversity of Chieti-Pescara · ITEngineering (Italy) · ITNational Research Council · ITImam Mohammad ibn Saud Islamic University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Premenopausal breast cancer (BC) is one of the most common cancers of women in rural Africa and part of the disease load may be related to hereditary predisposition, including mutations in the BRCA1 gene. However, the BRCA1 mutations associated with BC in Africa are scarcely characterized. We report here 33 BRCA1 point mutations, among which 2 novel missense variants, found in 59 Central Sudanese premenopausal BC patients. The high fractions of mutations with intercontinental and uniquely African distribution (17/33, 51.5 % and 14/33, 42.4 %, respectively) are in agreement with the high genetic diversity expected in an African population. Overall 24/33 variants (72.7 %) resulted neutral; 8/33 of unknown significance (24.3 %, including the 2 novel missense mutations); 1 (3.0 %) overtly deleterious. Notably, in silico studies predict that the novel C-terminal missense variant c.5090G>A (p.Cys1697Tyr) affects phosphopeptide recognition by the BRCA1 BRCT1 domain and may have a pathogenic impact. Genetic variation and frequency of unique or rare mutations of uncertain clinical relevance pose significant challenges to BRCA1 testing in Sudan, as it might happen in other low-resource rural African contexts.

Indexed as

Genes, BRCA1Point MutationPremenopauseAdultAmino Acid SequenceBRCA1 ProteinBreast NeoplasmsDNA Mutational AnalysisFemaleGenetic Predisposition to DiseaseHumansMiddle AgedMolecular Sequence DataMutation, MissensePolymerase Chain ReactionProtein Structure, QuaternaryBRCA1 Protein

Identifiers

PMID24729269
OpenAlexW2071512889

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.