Evidence map›Paper›PMID 33368296›Full record

ArticleInternational journal of cancer2021

Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.

Christine Lonjou, Séverine Eon-Marchais, Thérèse Truong, Marie-Gabrielle Dondon, Mojgan Karimi, Yue Jiao, Francesca Damiola, Laure Barjhoux, Dorothée Le Gal, Juana Beauvallet and 38 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. 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

48 authors at 20 institutions in 1 country.

Christine LonjouInserm, U900, Institut Curie, Paris, France.ORCID 0000-0003-1226-6992
Séverine Eon-MarchaisInserm, U900, Institut Curie, Paris, France.
Thérèse TruongUniversité Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.ORCID 0000-0002-2943-6786
Marie-Gabrielle DondonInserm, U900, Institut Curie, Paris, France.ORCID 0000-0001-6016-8524
Mojgan KarimiUniversité Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.
Yue JiaoInserm, U900, Institut Curie, Paris, France.
Francesca DamiolaDepartment of BioPathology, Centre Léon Bérard, Lyon, France.ORCID 0000-0002-0238-1252
Laure BarjhouxDepartment of BioPathology, Centre Léon Bérard, Lyon, France.
Dorothée Le GalInserm, U900, Institut Curie, Paris, France.
Juana BeauvalletInserm, U900, Institut Curie, Paris, France.
Noura MebiroukInserm, U900, Institut Curie, Paris, France.
Eve CavaciutiInserm, U900, Institut Curie, Paris, France.
Jean ChiesaCHRU Hôpital Caremeau, Nîmes, France.
Anne FloquetInstitut Bergonié, Bordeaux, France.
Séverine Audebert-BellangerDépartement de Génétique Médicale et Biologie de la Reproduction, CHU Brest, Hôpital Morvan, Brest, France.
Sophie GiraudService de Génétique, Hospices Civils de Lyon, Groupement Hospitalier Est, Bron, France.
Thierry FrebourgDépartement de Génétique, Hôpital Universitaire de Rouen, Rouen, France.
Jean-Marc LimacherService d'Onco-Hématologie, Hôpital Pasteur, Colmar, France.ORCID 0000-0002-7723-5508
Laurence GladieffService d'Oncologie Médicale, Institut Claudius Regaud-IUCT-Oncopole, Toulouse, France.ORCID 0000-0002-6980-9719
Isabelle MortemousqueService de Génétique, Hôpital Bretonneau, Tours, France.
Hélène DreyfusClinique Sainte Catherine, Avignon, France.
Sophie Lejeune-DumoulinService de Génétique Clinique Guy Fontaine, CHU Lille, Lille, France.
Christine LassetUniversité Claude Bernard Lyon 1, Villeurbanne, France.
Laurence Venat-BouvetService d'Oncologie Médicale, Hôpital Universitaire Dupuytren, Limoges, France.ORCID 0000-0002-0716-2550
Yves-Jean BignonDépartement d'Oncogénétique, Université Clermont Auvergne, UMR INSERM, U1240, Centre Jean Perrin, Clermont Ferrand, France.ORCID 0000-0001-9378-6353
Pascal PujolHôpital Arnaud de Villeneuve, CHU Montpellier, Service de Génétique Médicale et Oncogénétique, Montpellier, France.ORCID 0000-0001-8315-4715
Christine M MaugardDépartement d'Oncobiologie, LBBM, Hôpitaux Universitaires de Strasbourg, Génétique Oncologique Moléculaire, UF1422, Strasbourg, France.
Elisabeth LuporsiICL Alexis Vautrin, Unité d'Oncogénétique, Vandœuvre-lès-Nancy, France.
Valérie BonadonaUniversité Claude Bernard Lyon 1, Villeurbanne, France.
Catherine NoguèsDépartement d'Anticipation et de Suivi des Cancers, Oncogénétique Clinique, Institut Paoli-Calmettes, Marseille, France.
Pascaline BerthetDépartement de Biopathologie, Centre François Baclesse, Oncogénétique, Caen, France.
Capucine DelnatteInstitut de Cancérologie de l'Ouest, Unité d'Oncogénétique, Saint Herblain, France.
Paul GestaCH Georges Renon, Service d'Oncogénétique Régional Poitou-Charentes, Niort, France.
Alain LortholaryCentre Catherine de Sienne, Service d'Oncologie Médicale, Nantes, France.
Laurence FaivreInstitut GIMI, CHU de Dijon, Hôpital d'Enfants, Dijon, France.
Bruno BuecherInstitut Curie, Service de Génétique, Paris, France.
Olivier CaronDépartement de Médecine Oncologique, Gustave Roussy, Villejuif, France.ORCID 0000-0001-8934-2071
Marion Gauthier-VillarsInstitut Curie, Service de Génétique, Paris, France.
Isabelle CoupierHôpital Arnaud de Villeneuve, CHU Montpellier, Service de Génétique Médicale et Oncogénétique, Montpellier, France.
Sylvie MazoyerEquipe GENDEV, Centre de Recherche en Neurosciences de Lyon, Inserm U1028, CNRS UMR5292, Université Lyon 1, Université St Etienne, Lyon, France.ORCID 0000-0002-2135-0160
Luis-Cristobal MonrazInserm, U900, Institut Curie, Paris, France.
Maria KondratovaInserm, U900, Institut Curie, Paris, France.
Inna KupersteinInserm, U900, Institut Curie, Paris, France.ORCID 0000-0001-8086-8915
Pascal GuénelUniversité Paris-Saclay, UVSQ, Inserm, CESP, Villejuif, France.ORCID 0000-0002-8359-518X
Emmanuel BarillotInserm, U900, Institut Curie, Paris, France.ORCID 0000-0003-2724-2002
Dominique Stoppa-LyonnetInstitut Curie, Service de Génétique, Paris, France.ORCID 0000-0002-5438-8309
Nadine AndrieuInserm, U900, Institut Curie, Paris, France.
Fabienne LesueurInserm, U900, Institut Curie, Paris, France.ORCID 0000-0001-7404-4549
Inserm · FRUniversité Claude Bernard Lyon 1 · FRCentre Léon Bérard · FRInstitut Curie · FRCentre François Baclesse · FRCentre Georges François Leclerc · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Nîmes · FRCentre Hospitalier Universitaire de Rouen · FRCentre Hospitalier Universitaire de Tours · FRDélégation Paris 5 · FRHôpital Pasteur · FRHôpital Universitaire Dupuytren · FRHôpitaux Universitaires de Strasbourg · FRHospices Civils de Lyon · FRInstitut Bergonié · FRInstitut Claudius Regaud · FRInstitut de Cancérologie de Lorraine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-nucleotide polymorphisms (SNPs) in over 180 loci have been associated with breast cancer (BC) through genome-wide association studies involving mostly unselected population-based case-control series. Some of them modify BC risk of women carrying a BRCA1 or BRCA2 (BRCA1/2) mutation and may also explain BC risk variability in BC-prone families with no BRCA1/2 mutation. Here, we assessed the contribution of SNPs of the iCOGS array in GENESIS consisting of BC cases with no BRCA1/2 mutation and a sister with BC, and population controls. Genotyping data were available for 1281 index cases, 731 sisters with BC, 457 unaffected sisters and 1272 controls. In addition to the standard SNP-level analysis using index cases and controls, we performed pedigree-based association tests to capture transmission information in the sibships. We also performed gene- and pathway-level analyses to maximize the power to detect associations with lower-frequency SNPs or those with modest effect sizes. While SNP-level analyses identified 18 loci, gene-level analyses identified 112 genes. Furthermore, 31 Kyoto Encyclopedia of Genes and Genomes and 7 Atlas of Cancer Signaling Network pathways were highlighted (false discovery rate of 5%). Using results from the "index case-control" analysis, we built pathway-derived polygenic risk scores (PRS) and assessed their performance in the population-based CECILE study and in a data set composed of GENESIS-affected sisters and CECILE controls. Although these PRS had poor predictive value in the general population, they performed better than a PRS built using our SNP-level findings, and we found that the joint effect of family history and PRS needs to be considered in risk prediction models.

Indexed as

MutationPolymorphism, Single NucleotideBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCase-Control StudiesFemaleGene Regulatory NetworksGenetic Predisposition to DiseaseGenetic TestingGenome-Wide Association StudyHumansProtein Interaction MapsROC CurveSiblingsSignal TransductionBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanassociation studyfamilial breast cancersingle-nucleotide polymorphismsystems biology

Identifiers

PMID33368296
PMCPMC9290690
OpenAlexW3116159660

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.