Evidence map›Paper›PMID 21466675›Full record

ArticleBreast cancer research : BCR2011

Exploring the link between MORF4L1 and risk of breast cancer.

Griselda Martrat, Christopher M Maxwell, Emiko Tominaga, Montserrat Porta-de-la-Riva, Núria Bonifaci, Laia Gómez-Baldó, Massimo Bogliolo, Conxi Lázaro, Ignacio Blanco, Joan Brunet and 124 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  12. The Role of PALB2 in the DNA Damage Response and Cancer Predisposition.International journal of molecular sciences · 2017
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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

134 authors at 20 institutions in 15 countries.

Griselda MartratTranslational Research Laboratory, Catalan Institute of Oncology, Bellvitge Institute for Biomedical Research (IDIBELL), Gran Via 199, L'Hospitalet del Llobregat 08908, Spain.
Christopher M Maxwell
Emiko Tominaga
Montserrat Porta-de-la-Riva
Núria Bonifaci
Laia Gómez-Baldó
Massimo Bogliolo
Conxi Lázaro
Ignacio Blanco
Joan Brunet
Helena Aguilar
Juana Fernández-Rodríguez
Sheila Seal
Anthony Renwick
Nazneen Rahman
Julia Kühl
Kornelia Neveling
Detlev Schindler
María J Ramírez
María Castellà
Gonzalo Hernández
EMBRACE
Douglas F Easton
Susan Peock
Margaret Cook
Clare T Oliver
Debra Frost
Radka Platte
D Gareth Evans
Fiona Lalloo
Rosalind Eeles
Louise Izatt
Carol Chu
Rosemarie Davidson
Kai-Ren Ong
Jackie Cook
Fiona Douglas
Shirley Hodgson
Carole Brewer
Patrick J Morrison
Mary Porteous
Paolo Peterlongo
Siranoush Manoukian
Bernard Peissel
Daniela Zaffaroni
Gaia Roversi
Monica Barile
Alessandra Viel
Barbara Pasini
Laura Ottini
Anna Laura Putignano
Antonella Savarese
Loris Bernard
Paolo Radice
Sue Healey
Amanda Spurdle
Xiaoqing Chen
Jonathan Beesley
kConFab
Matti A Rookus
Senno Verhoef
Madeleine A Tilanus-Linthorst
Maaike P Vreeswijk
Christi J Asperen
Danielle Bodmer
Margreet G E M Ausems
Theo A van Os
Marinus J Blok
Hanne E J Meijers-Heijboer
Frans B L Hogervorst
HEBON
David E Goldgar
Saundra Buys
Esther M John
Alexander Miron
Melissa Southey
Mary B Daly
BCFR
SWE-BRCA
Katja Harbst
Ake Borg
Johanna Rantala
Gisela Barbany-Bustinza
Hans Ehrencrona
Marie Stenmark-Askmalm
Bella Kaufman
Yael Laitman
Roni Milgrom
Eitan Friedman
Susan M Domchek
Katherine L Nathanson
Timothy R Rebbeck
Oskar Thor Johannsson
Fergus J Couch
Xianshu Wang
Zachary Fredericksen
Daniel Cuadras
Víctor Moreno
Friederike K Pientka
Reinhard Depping
Trinidad Caldés
Ana Osorio
Javier Benítez
Juan Bueren
Tuomas Heikkinen
Heli Nevanlinna
Ute Hamann
Diana Torres
Maria Adelaide Caligo
Andrew K Godwin
Evgeny N Imyanitov
Ramunas Janavicius
GEMO Study Collaborators
Olga M Sinilnikova
Dominique Stoppa-Lyonnet
Sylvie Mazoyer
Carole Verny-Pierre
Laurent Castera
Antoine de Pauw
Yves-Jean Bignon
Nancy Uhrhammer
Jean-Philippe Peyrat
Philippe Vennin
Sandra Fert Ferrer
Marie-Agnès Collonge-Rame
Isabelle Mortemousque
Lesley McGuffog
Georgia Chenevix-Trench
Olivia M Pereira-Smith
Antonis C Antoniou
Julián Cerón
Kaoru Tominaga
Jordi Surrallés
Miguel Angel Pujana
Institut d'Investigació Biomédica de Bellvitge · ESUniversity of Cambridge · GBQIMR Berghofer Medical Research Institute · AUMayo Clinic · USUniversitat Autònoma de Barcelona · ESThe University of Texas Health Science Center at San Antonio · USUniversité Claude Bernard Lyon 1 · FRHelsinki University Hospital · FIRipamonti · ITInstitute of Cancer Research · GBIstituti di Ricovero e Cura a Carattere Scientifico · ITKarolinska University Hospital · SESheba Medical Center · ILUniversity of Würzburg · DEBirmingham Women's Hospital · GBCentro de Investigación Biomédica en Red · ESFox Chase Cancer Center · USGuy's Hospital · GBHarvard University · USHeidelberg University · DE

Funding

A genome-wide association study for breast cancer in BRCA1 mutation carriersR01CA128978 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2008 to 2012
$4.8M
Role of MRG15 in Chromatin Changes During Cell Senescence and In Vivo AgingR01AG032134 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LECHLEITER, JAMES D · 2007 to 2011
$1.5M
Cancer Research UK 10118Cancer Research UK 11022Cancer Research UK 11174NCI NIH HHS R01 CA128978NIA NIH HHS R01 AG032134
6 · The paper itself

Abstract

introductionProteins encoded by Fanconi anemia (FA) and/or breast cancer (BrCa) susceptibility genes cooperate in a common DNA damage repair signaling pathway. To gain deeper insight into this pathway and its influence on cancer risk, we searched for novel components through protein physical interaction screens.

methodsProtein physical interactions were screened using the yeast two-hybrid system. Co-affinity purifications and endogenous co-immunoprecipitation assays were performed to corroborate interactions. Biochemical and functional assays in human, mouse and Caenorhabditis elegans models were carried out to characterize pathway components. Thirteen FANCD2-monoubiquitinylation-positive FA cell lines excluded for genetic defects in the downstream pathway components and 300 familial BrCa patients negative for BRCA1/2 mutations were analyzed for genetic mutations. Common genetic variants were genotyped in 9,573 BRCA1/2 mutation carriers for associations with BrCa risk.

resultsA previously identified co-purifying protein with PALB2 was identified, MRG15 (MORF4L1 gene). Results in human, mouse and C. elegans models delineate molecular and functional relationships with BRCA2, PALB2, RAD51 and RPA1 that suggest a role for MRG15 in the repair of DNA double-strand breaks. Mrg15-deficient murine embryonic fibroblasts showed moderate sensitivity to γ-irradiation relative to controls and reduced formation of Rad51 nuclear foci. Examination of mutants of MRG15 and BRCA2 C. elegans orthologs revealed phenocopy by accumulation of RPA-1 (human RPA1) nuclear foci and aberrant chromosomal compactions in meiotic cells. However, no alterations or mutations were identified for MRG15/MORF4L1 in unclassified FA patients and BrCa familial cases. Finally, no significant associations between common MORF4L1 variants and BrCa risk for BRCA1 or BRCA2 mutation carriers were identified: rs7164529, Ptrend = 0.45 and 0.05, P2df = 0.51 and 0.14, respectively; and rs10519219, Ptrend = 0.92 and 0.72, P2df = 0.76 and 0.07, respectively.

conclusionsWhile the present study expands on the role of MRG15 in the control of genomic stability, weak associations cannot be ruled out for potential low-penetrance variants at MORF4L1 and BrCa risk among BRCA2 mutation carriers.

Indexed as

AnimalsBreast NeoplasmsCaenorhabditis elegansCell LineDNA DamageDNA RepairFanconi AnemiaFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group N ProteinFemaleGenes, BRCA1Genes, BRCA2Genetic Predisposition to DiseaseHumansMiceMutationFANCD2 protein, humanFanconi Anemia Complementation Group D2 ProteinFanconi Anemia Complementation Group N ProteinMORF4L1 protein, humanNuclear ProteinsPALB2 protein, humanRad51 RecombinaseReplication Protein ARPA1 protein, humanTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID21466675
PMCPMC3219203
OpenAlexW2114023115

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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.