Evidence map›Paper›PMID 29511213›Full record

ArticleNature communications2018

Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1.

Gonzalo Hernández, María José Ramírez, Jordi Minguillón, Paco Quiles, Gorka Ruiz de Garibay, Miriam Aza-Carmona, Massimo Bogliolo, Roser Pujol, Rosario Prados-Carvajal, Juana Fernández and 16 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

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  19. High content drug screening for Fanconi anemia therapeutics.Orphanet journal of rare diseases · 2020
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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

26 authors at 10 institutions in 3 countries.

Gonzalo HernándezDepartment of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
María José RamírezDepartment of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Jordi MinguillónDepartment of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Paco QuilesHereditary Cancer Programme, Catalan Institute of Oncology (ICO), Bellvitge Institute for Biomedical Research (IDIBELL), L'Hospitalet del Llobregat, Barcelona, 08908, Spain.
Gorka Ruiz de GaribayBreast Cancer and Systems Biology Laboratory, Program Against Cancer Therapeutic Resistance (ProCURE), ICO, IDIBELL, L'Hospitalet del Llobregat, Barcelona, 08908, Spain.
Miriam Aza-CarmonaDepartment of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Massimo BoglioloDepartment of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Roser PujolDepartment of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain.
Rosario Prados-CarvajalCentro Andaluz de Biología Molecular y Medicina Regenerativa (CABIMER) and Departamento de Genética, Universidad de Sevilla, Sevilla, 41080, Spain.
Juana FernándezHereditary Cancer Programme, Catalan Institute of Oncology (ICO), Bellvitge Institute for Biomedical Research (IDIBELL), L'Hospitalet del Llobregat, Barcelona, 08908, Spain.
Nadia GarcíaBreast Cancer and Systems Biology Laboratory, Program Against Cancer Therapeutic Resistance (ProCURE), ICO, IDIBELL, L'Hospitalet del Llobregat, Barcelona, 08908, Spain.
Adrià LópezHereditary Cancer Programme, ICO, Girona Biomedical Research Institute (IDIBGI), Girona, 17007, Spain.
Sara Gutiérrez-EnríquezOncogenetics Group, Vall d´Hebron Institute of Oncology (VHIO), Barcelona, 08035, Spain.
Orland DiezOncogenetics Group, Vall d´Hebron Institute of Oncology (VHIO), Barcelona, 08035, Spain.
Javier BenítezCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, 08193, Spain.
Mónica SalinasHereditary Cancer Programme, Catalan Institute of Oncology (ICO), Bellvitge Institute for Biomedical Research (IDIBELL), L'Hospitalet del Llobregat, Barcelona, 08908, Spain.
Alex TeuléHereditary Cancer Programme, Catalan Institute of Oncology (ICO), Bellvitge Institute for Biomedical Research (IDIBELL), L'Hospitalet del Llobregat, Barcelona, 08908, Spain.
Joan BrunetHereditary Cancer Programme, Catalan Institute of Oncology (ICO), Bellvitge Institute for Biomedical Research (IDIBELL), L'Hospitalet del Llobregat, Barcelona, 08908, Spain.ORCID http://orcid.org/0000-0003-1945-3512
Paolo RadiceDepartment of Preventive and Predictive Medicine, Unit of Molecular Bases of Genetic Risk and Genetic Testing, Fondazione IRCCS (Istituto Di Ricovero e Cura a Carattere Scientifico) Istituto Nazionale dei Tumori (INT), Milan, 20133, Italy.
Paolo PeterlongoDepartment of Preventive and Predictive Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, IFOM, Fondazione Istituto FIRC di Oncologia Molecolare and Unit of Molecular Bases of Genetic Risk and Genetic Testing, Milan, 20139, Italy.
Detlev SchindlerDepartment of Human Genetics, Wurzburg University, Wurzburg, 97070, Germany.
Pablo HuertasCentro Andaluz de Biología Molecular y Medicina Regenerativa (CABIMER) and Departamento de Genética, Universidad de Sevilla, Sevilla, 41080, Spain.ORCID http://orcid.org/0000-0002-1756-4449
Xose S PuenteDepartment of Biochemistry and Molecular Biology, Instituto Universitario de Oncología, Universidad de Oviedo, Oviedo, 33006, Spain.
Conxi LázaroHereditary Cancer Programme, Catalan Institute of Oncology (ICO), Bellvitge Institute for Biomedical Research (IDIBELL), L'Hospitalet del Llobregat, Barcelona, 08908, Spain.
Miquel Àngel PujanaBreast Cancer and Systems Biology Laboratory, Program Against Cancer Therapeutic Resistance (ProCURE), ICO, IDIBELL, L'Hospitalet del Llobregat, Barcelona, 08908, Spain. mapujana@iconcologia.net.
Jordi SurrallésDepartment of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, 08193, Spain. jsurralles@santpau.cat.
Institut d'Investigació Biomédica de Bellvitge · ESUniversitat Autònoma de Barcelona · ESCentro Andaluz de Biología Molecular y Medicina Regenerativa · ESFondazione IRCCS Istituto Nazionale dei Tumori · ITInstitut d'Investigació Biomèdica de Girona · ESSpanish National Cancer Research Centre · ESUniversidad de Oviedo · ESUniversity of Würzburg · DEVall d'Hebron Hospital Universitari · ESVall d'Hebron Institute of Oncology · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BRCA1 is a tumor suppressor that regulates DNA repair by homologous recombination. Germline mutations in BRCA1 are associated with increased risk of breast and ovarian cancer and BRCA1 deficient tumors are exquisitely sensitive to poly (ADP-ribose) polymerase (PARP) inhibitors. Therefore, uncovering additional components of this DNA repair pathway is of extreme importance for further understanding cancer development and therapeutic vulnerabilities. Here, we identify EDC4, a known component of processing-bodies and regulator of mRNA decapping, as a member of the BRCA1-BRIP1-TOPBP1 complex. EDC4 plays a key role in homologous recombination by stimulating end resection at double-strand breaks. EDC4 deficiency leads to genome instability and hypersensitivity to DNA interstrand cross-linking drugs and PARP inhibitors. Lack-of-function mutations in EDC4 were detected in BRCA1/2-mutation-negative breast cancer cases, suggesting a role in breast cancer susceptibility. Collectively, this study recognizes EDC4 with a dual role in decapping and DNA repair whose inactivation phenocopies BRCA1 deficiency.

Indexed as

DNA RepairBRCA1 ProteinBreast NeoplasmsCarrier ProteinsDNA-Binding ProteinsFemaleHomologous RecombinationHumansMutationNuclear ProteinsPoly (ADP-Ribose) Polymerase-1Protein BindingProteinsRNA CapsBRCA1 ProteinBRCA1 protein, humanCarrier ProteinsDNA-Binding ProteinsEDC4 protein, humanNuclear ProteinsPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1ProteinsRNA CapsTOPBP1 protein, human

Identifiers

PMID29511213
PMCPMC5840268
OpenAlexW2790626243

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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.