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dc.contributor.authorSawyer, Elinor
dc.contributor.authorRoylance, Rebecca
dc.contributor.authorPetridis, Christos
dc.contributor.authorBrook, Mark N.
dc.contributor.authorNowinski, Salpie
dc.contributor.authorPapouli, Efterpi
dc.contributor.authorFletcher, Olivia
dc.contributor.authorPinder, Sarah
dc.contributor.authorHanby, Andrew
dc.contributor.authorKohut, Kelly
dc.contributor.authorGorman, Patricia
dc.contributor.authorCaneppele, Michele
dc.contributor.authorPeto, Julian
dc.contributor.authorSilva, Isabel dos Santos
dc.date.accessioned2014-08-12T07:07:49Z
dc.date.available2014-08-12T07:07:49Z
dc.date.issued2014
dc.identifier.issn1553-7390
dc.identifier.urihttp://hdl.handle.net/11343/41099
dc.description.abstractInvasive lobular breast cancer (ILC) accounts for 10-15% of all invasive breast carcinomas. It is generally ER positive (ER+) and often associated with lobular carcinoma in situ (LCIS). Genome-wide association studies have identified more than 70 common polymorphisms that predispose to breast cancer, but these studies included predominantly ductal (IDC) carcinomas. To identify novel common polymorphisms that predispose to ILC and LCIS, we pooled data from 6,023 cases (5,622 ILC, 401 pure LCIS) and 34,271 controls from 36 studies genotyped using the iCOGS chip. Six novel SNPs most strongly associated with ILC/LCIS in the pooled analysis were genotyped in a further 516 lobular cases (482 ILC, 36 LCIS) and 1,467 controls. These analyses identified a lobular-specific SNP at 7q34 (rs11977670, OR (95% CI) for ILC = 1.13 (1.09-1.18), P = 6.0x10(-10); P-het for ILC vs IDC ER+ tumors = 1.8x10(-4)). Of the 75 known breast cancer polymorphisms that were genotyped, 56 were associated with ILC and 15 with LCIS at P<0.05. Two SNPs showed significantly stronger associations for ILC than LCIS (rs2981579/10q26/FGFR2, P-het = 0.04 and rs889312/5q11/MAP3K1, P-het = 0.03); and two showed stronger associations for LCIS than ILC (rs6678914/1q32/LGR6, P-het = 0.001 and rs1752911/6q14, P-het = 0.04). In addition, seven of the 75 known loci showed significant differences between ER+ tumors with IDC and ILC histology, three of these showing stronger associations for ILC (rs11249433/1p11, rs2981579/10q26/FGFR2 and rs10995190/10q21/ZNF365) and four associated only with IDC (5p12/rs10941679; rs2588809/14q24/RAD51L1, rs6472903/8q21 and rs1550623/2q31/CDCA7). In conclusion, we have identified one novel lobular breast cancer specific predisposition polymorphism at 7q34, and shown for the first time that common breast cancer polymorphisms predispose to LCIS. We have shown that many of the ER+ breast cancer predisposition loci also predispose to ILC, although there is some heterogeneity between ER+ lobular and ER+ IDC tumors. These data provide evidence for overlapping, but distinct etiological pathways within ER+ breast cancer between morphological subtypes.
dc.publisherPUBLIC LIBRARY SCIENCE
dc.titleGenetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast
dc.typeJournal Article
dc.identifier.doi10.1371/journal.pgen.1004285
melbourne.affiliation.departmentMelbourne Students & Learning
melbourne.source.titlePLOS GENETICS
melbourne.source.monthAPR
melbourne.source.volume10
melbourne.source.issue4
melbourne.identifier.nhmrc288704
melbourne.identifier.nhmrc454508
melbourne.publicationid253733
melbourne.publication.chiefinvestigatorPHILLIPS, PROF KELLY-ANNE KELLY
melbourne.publication.chiefinvestigatorPHILLIPS, PROF KELLY-ANNE KELLY
melbourne.publication.chiefinvestigatoremailkphi@unimelb.edu.au
melbourne.publication.chiefinvestigatoremailkphi@unimelb.edu.au
melbourne.elementsidNA
melbourne.contributor.authorAPICELLA, CARMEL
melbourne.contributor.authorHopper, John
melbourne.contributor.authorBaglietto, Laura
melbourne.contributor.authorMilne, Roger
melbourne.contributor.authorGiles, Graham
melbourne.contributor.authorSouthey, Melissa
melbourne.contributor.authorSeveri, Gianluca
melbourne.internal.ingestnoteAbstract bulk upload (2017-07-24)
melbourne.accessrightsThis item is currently not available from this repository


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