Evidence map›Paper›PMID 26785832›Full record

ArticleEuropean journal of human genetics : EJHG2016

Mutation screening of MIR146A/B and BRCA1/2 3'-UTRs in the GENESIS study.

Amandine I Garcia, Monique Buisson, Francesca Damiola, Chloé Tessereau, Laure Barjhoux, Carole Verny-Pierre, Valérie Sornin, Marie-Gabrielle Dondon, Séverine Eon-Marchais, GENESIS investigators and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Functional Analysis ofThe application of clinical genetics · 2024
    Article
  2. miR-146a inhibits ovarian tumor growthMolecular therapy oncolytics · 2023
    Article
  3. Article
  4. Genetic Variants in the 3'UTR ofDiagnostics (Basel, Switzerland) · 2020
    Article
  5. Non-Coding Variants inCancers · 2018
    Review
  6. Article
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

26 authors at 10 institutions in 1 country.

Amandine I GarciaCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Monique BuissonCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Francesca DamiolaCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Chloé TessereauCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Laure BarjhouxCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Carole Verny-PierreCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Valérie SorninCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Marie-Gabrielle DondonINSERM, U900, Paris, France.
Séverine Eon-MarchaisINSERM, U900, Paris, France.
GENESIS investigators
Olivier CaronDépartement de Médecine Oncologique, Institut de Cancérologie Gustave Roussy, Villejuif, France.
Marion Gautier-VillarsInstitut Curie, Service de Génétique, Paris, France.
Isabelle CoupierHôpital Arnaud de Villeneuve, CHU Montpellier, Service de Génétique médicale et Oncogénétique, Montpellier, France.
Bruno BuecherInstitut Curie, Service de Génétique, Paris, France.
Philippe VenninCentre Oscar Lambret, Lille, France.
Muriel BelottiInstitut Curie, Service de Génétique, Paris, France.
Alain LortholaryCentre Catherine de Sienne, Service d'Oncologie Médicale, Nantes, France.
Paul GestaCH Georges Renon, Service Oncogénétique pour la consultation oncogénétique régionale Poitou-Charentes, Niort, France.
Catherine DugastCentre Eugène Marquis, Service de Génétique, Rennes, France.
Catherine NoguèsInstitut Curie, Service de Génétique, Paris, France.
Jean-Pierre FrickerCentre Paul Strauss, Unité d'Oncologie, Strasbourg, France.
Laurence FaivreHôpital d'Enfants, Service de Génétique Médicale, Dijon, France.
Dominique Stoppa-LyonnetInstitut Curie, Service de Génétique, Paris, France.
Nadine AndrieuINSERM, U900, Paris, France.
Olga M SinilnikovaCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Sylvie MazoyerCancer Research Centre of Lyon, CNRS UMR5286/Inserm U1052/Université Lyon 1, Centre Léon Bérard, Lyon, France.
Université Claude Bernard Lyon 1 · FRCEA Valduc · FRCentre Eugène Marquis · FRCentre Oscar Lambret · FRDélégation Paris 5 · FRInserm · FRInstitut Curie · FRCentre Georges François Leclerc · FRGroupe d’Etude des Cétacés du Cotentin · FRInstitut Gustave Roussy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although a wide number of breast cancer susceptibility alleles associated with various levels of risk have been identified to date, about 50% of the heritability is still missing. Although the major BRCA1 and BRCA2 genes are being extensively screened for truncating and missense variants in breast and/or ovarian cancer families, potential regulatory variants affecting their expression remain largely unexplored. In an attempt to identify such variants, we focused our attention on gene regulation mediated by microRNAs (miRs). We screened two genes, MIR146A and MIR146B, producing miR-146a and miR-146b-5p, respectively, that regulate BRCA1, and the 3'- untranslated regions (3'-UTRs) of BRCA1 and BRCA2 in the GENESIS French national case/control study (BRCA1- and BRCA2-negative breast cancer cases with at least one sister with breast cancer and matched controls). We identified one rare variant in MIR146A, four in MIR146B, five in BRCA1 3'-UTR and one in BRCA2 3'-UTR in 716 index cases and 619 controls. Among these 11 rare variants, 7 were identified each in 1 index case. None of the three relevant MIR146A/MIR146B variants affected the pre-miR sequences. The potential causality of the four relevant BRCA1/BRCA2 3'-UTRs variants was evaluated with luciferase reporter assays and co-segregation studies, as well as with bioinformatics analyses to predict miRs-binding sites, RNA secondary structures and RNA accessibility. This is the first study to report the screening of miR genes and of BRCA2 3'-UTR in a large series of familial breast cancer cases. None of the variant identified in this study gave convincing evidence of potential pathogenicity.

Indexed as

3' Untranslated RegionsMutationAdultAgedBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCase-Control StudiesFemaleHeLa CellsHumansMCF-7 CellsMicroRNAsMiddle Aged3' Untranslated RegionsBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanMicroRNAsMIRN146 microRNA, human

Identifiers

PMID26785832
PMCPMC4989198
OpenAlexW2419896901

What OpenQuestion holds

Textmetadata
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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.