Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/23123
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBalleine, R.-
dc.contributor.authorMurali, R.-
dc.contributor.authorBilous, A.-
dc.contributor.authorFarshid, G.-
dc.contributor.authorWaring, P.-
dc.contributor.authorProvan, P.-
dc.contributor.authorByth, K.-
dc.contributor.authorThorne, H.-
dc.contributor.authorKirk, J.-
dc.date.issued2006-
dc.identifier.citationHistopathology, 2006; 49(5):523-532-
dc.identifier.issn0309-0167-
dc.identifier.issn1365-2559-
dc.identifier.urihttp://hdl.handle.net/2440/23123-
dc.descriptionJournal compilation © 2009 Blackwell Publishing Ltd-
dc.description.abstract<h4>Aims</h4>Germline variants in the ataxia telangiectasia mutated (ATM) gene have been implicated in increased breast cancer risk. The aim of this study was to determine whether the histopathology of breast cancers occurring in ATM variant carriers is distinctive or resembles the described BRCA1 mutation-associated phenotype.<h4>Methods</h4>The histopathological features of breast cancers occurring in ATM variant carriers from multiple-case breast cancer families were compared with matched controls. The test group included 21 cases of in situ and/or invasive cancer from carriers of either the IVS10-6T-->G, 2424V-->G or 1420L-->F ATM variants in the absence of BRCA1 or BRCA2 mutations. An additional four invasive cancers from carriers of a pathogenic BRCA1 mutation in the context of a familial ATM variant were also examined.<h4>Results</h4>The histopathology of breast cancers in ATM variant-only carriers was not significantly different from controls and known features of BRCA1 mutation-associated cancer were rarely seen. In contrast, these features were prominent in the small group of cases with a pathogenic BRCA1 mutation.<h4>Conclusions</h4>Breast cancer occurring in carriers of ATM variants is not associated with distinctive histopathological features and does not resemble the tumour phenotype commonly observed in BRCA1 mutation carriers.-
dc.description.statementofresponsibilityR L Balleine, R Murali, A M Bilous, G Farshid, P Waring, P Provan, K Byth, H Thorne, ConFab Investigators & J A Kirk-
dc.language.isoen-
dc.publisherBlackwell Science Ltd-
dc.source.urihttp://dx.doi.org/10.1111/j.1365-2559.2006.02538.x-
dc.subjectAtaxia-Telangiectasia Families-
dc.subjectGermline Mutations-
dc.subjectEstrogen-Receptor-
dc.subjectBRCA2 Mutations-
dc.subjectSusceptibility-
dc.subjectRisk-
dc.subjectCarcinoma-
dc.subjectPathology-
dc.subjectAge-
dc.subjectPhenotypes-
dc.titleHistopathological features of breast cancer in carriers of ATM gene variants-
dc.typeJournal article-
dc.identifier.doi10.1111/j.1365-2559.2006.02538.x-
pubs.publication-statusPublished-
dc.identifier.orcidFarshid, G. [0000-0002-2056-0561]-
Appears in Collections:Aurora harvest 2
Pathology publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.