Evidence map›Paper›PMID 26026974›Full record

ArticleFamilial cancer2015

BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study.

Inmaculada de Juan, Sarai Palanca, Asunción Domenech, Lidia Feliubadaló, Ángel Segura, Ana Osorio, Isabel Chirivella, Miguel de la Hoya, Ana Beatriz Sánchez, Mar Infante and 18 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Familial cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.2field-weighted citation impact, top 34% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Molecular characteristics of Asian male BRCA-related cancers.Breast cancer research and treatment · 2023
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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

28 authors at 12 institutions in 2 countries.

Inmaculada de JuanLaboratory of Molecular Biology, Service of Clinical Analysis, University and Polytechnic Hospital La Fe, Escuela de Enfermería 7ª planta. Avd. Campanar 21, Valencia, 46009, Spain. dejuan_inm@gva.es.
Sarai PalancaLaboratory of Molecular Biology, Service of Clinical Analysis, University and Polytechnic Hospital La Fe, Escuela de Enfermería 7ª planta. Avd. Campanar 21, Valencia, 46009, Spain.
Asunción DomenechLaboratory of Molecular Biology, Service of Clinical Analysis, University and Polytechnic Hospital La Fe, Escuela de Enfermería 7ª planta. Avd. Campanar 21, Valencia, 46009, Spain.
Lidia FeliubadalóHereditary Cancer Program, Catalan Institute of Oncology (ICO), L'Hospitalet de Llobregat (Barcelona), Spain.
Ángel SeguraUnit of Genetic Counseling in Cancer, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Ana OsorioHuman Genetics Group, Human Cancer Genetics Programme, Spanish National Cancer Research Centre and Spanish Network on Rare Diseases (CIBERER), Madrid, Spain.
Isabel ChirivellaUnit of Genetic Counseling in Cancer, Hospital Clínico, Valencia, Spain.
Miguel de la HoyaMolecular Oncology Laboratory, IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
Ana Beatriz SánchezUnit of Genetic Counseling in Cancer, Hospital General de Elche, Elche, Spain.
Mar InfanteCancer Genetic Group, Institute of Genetics and Molecular Biology (UVa-CSIC), Valladolid, Spain.
Isabel TenaUnit of Genetic Counseling in Cancer, Hospital General de Castellón, Castellón, Spain.
Orland DíezOncogenetics Laboratory, University Hospital Vall d'Hebron, Vall d'Hebron Institute of Oncology (VHIO), Universitat Autònoma de Barcelona, Barcelona, Spain.
Zaida Garcia-CasadoLaboratory of Molecular Biology, Valencian Institute of Oncology (IVO), Valencia, Spain.
Ana VegaFundación Pública Galega de Medicina Xenómica-SERGAS, Grupo de Medicina Xenómica-USC, IDIS, CIBERER, Santiago de Compostela, Spain.
Àlex TeuléHereditary Cancer Program, Catalan Institute of Oncology (ICO), L'Hospitalet de Llobregat (Barcelona), Spain.
Alicia BarrosoHuman Genetics Group, Human Cancer Genetics Programme, Spanish National Cancer Research Centre and Spanish Network on Rare Diseases (CIBERER), Madrid, Spain.
Pedro PérezDepartment of Oncology, IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
Mercedes DuránCancer Genetic Group, Institute of Genetics and Molecular Biology (UVa-CSIC), Valladolid, Spain.
Estela CarrascoHigh Risk and Prevention Unit, University Hospital Vall d'Hebron, Barcelona, Spain.
M José Juan-FitaUnit of Genetic Counseling in Cancer, IVO, Valencia, Spain.
Rosa MurriaLaboratory of Molecular Biology, Service of Clinical Analysis, University and Polytechnic Hospital La Fe, Escuela de Enfermería 7ª planta. Avd. Campanar 21, Valencia, 46009, Spain.
Marta LlopLaboratory of Molecular Biology, Service of Clinical Analysis, University and Polytechnic Hospital La Fe, Escuela de Enfermería 7ª planta. Avd. Campanar 21, Valencia, 46009, Spain.
Eva BarraganLaboratory of Molecular Biology, Service of Clinical Analysis, University and Polytechnic Hospital La Fe, Escuela de Enfermería 7ª planta. Avd. Campanar 21, Valencia, 46009, Spain.
Ángel IzquierdoHereditary Cancer Program, Catalan Institute of Oncology (ICO), L'Hospitalet de Llobregat (Barcelona), Spain.
Javier BenítezHuman Genetics Group and Genotyping Unit, Human Cancer Genetics Programme, Spanish National Cancer Research Centre and Spanish Network on Rare Diseases (CIBERER), Madrid, Spain.
Trinidad CaldésMolecular Oncology Laboratory, IdISSC, Hospital Clínico San Carlos, Madrid, Spain.
Dolores SalasGeneral Directorate Public Health and Centre for Public Health Research (CSISP), Valencia Genetic Counseling in Cancer Programme, Valencia, Spain.
Pascual BoluferLaboratory of Molecular Biology, Service of Clinical Analysis, University and Polytechnic Hospital La Fe, Escuela de Enfermería 7ª planta. Avd. Campanar 21, Valencia, 46009, Spain. bolufer_pas@gva.es.
Hospital Universitari i Politècnic La Fe · ESInstitut Català d'Oncologia · ESInstituto de Biomedicina y Genética Molecular de Valladolid · ESInstituto de Investigación Sanitaria del Hospital Clínico San Carlos · ESSpanish National Cancer Research Centre · ESCentre for Biomedical Network Research on Rare Diseases · ESHospital Clínico San Carlos · ESHospital Clínico Universitario de Valencia · ESHospital General Universitari de Castelló · ESHospital General Universitario de Elche · ESServicio Gallego de Salud · ESVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Male breast cancer (MBC) is a rare disease that represents <1% of all breast cancers (BCs). We analyze the results of a multicenter study performed in Spanish familial MBC including family history of hereditary breast and ovarian cancer syndrome (HBOCS) and clinicopathological features. We also study the relationship between BRCA1/BRCA2 mutational status in male relatives affected with cancer (MAC) and, family history and tumor types. The study included 312 men index cases with family history of HBOCS and 61 MAC BRCA1/2 mutation-carriers. Family history, histological grade (HG), clinicopathological and immunohistochemistry data were collected. BRCA1/2 mutation analyses were performed by direct sequencing or screening methods and the large rearrangements by multiplex ligation dependent probe amplification. We found 49 mutation-carriers (15.7%), 95.9% with BRCA2 mutations. BRCA2 mutation-carriers were associated with families with at least one MBC and one BC in female (type II; p = 0.05). Strong association were found between the presence of pathogenic mutations in MBCs and the advanced HG (p = 0.003). c.658_659delTG, c.2808_2811delACAA, c.6275_6276delTT and c.9026_9030delATCAT were the most prevalent mutations. In 61 MAC we found 20 mutations in BRCA1 and 41 in BRCA2. For MAC we show that mutational status was differentially associated with family history (p = 0.018) and tumor type, being BRCA2 mutations linked with BC and prostatic cancer (p = 0.018). MBC caused by BRCA1/2 mutations define two types of MBCs. The most frequent caused by BRCA2 mutation linked to type II families and the rarest one attributed to BRCA1 mutation. Tumor associated with MAC suggest that only BRCA2 mutations have to do with a specific type of cancer (BC and prostatic cancer); but the linkage to tumors is questionable for BRCA1 mutations .

Indexed as

Genetic Predisposition to DiseaseAdultAgedAged, 80 and overBiomarkers, TumorBRCA1 ProteinBRCA2 ProteinBreast Neoplasms, MaleCarcinoma, Ductal, BreastCarcinoma, LobularFemaleFollow-Up StudiesGenetic TestingGerm-Line MutationHumansImmunoenzyme TechniquesBiomarkers, TumorBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanBRCA1BRCA2 mutationsFamilial male breast cancerHereditary breast and ovarian cancer syndrome

Identifiers

PMID26026974
OpenAlexW576226737

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Registered trials

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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.