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Region Hovedstaden - en del af Københavns Universitetshospital
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Genetic predisposition to in situ and invasive lobular carcinoma of the breast

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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  • Elinor Sawyer
  • Rebecca Roylance
  • Christos Petridis
  • Mark N Brook
  • Salpie Nowinski
  • Efterpi Papouli
  • Olivia Fletcher
  • Sarah Pinder
  • Andrew Hanby
  • Kelly Kohut
  • Patricia Gorman
  • Michele Caneppele
  • Julian Peto
  • Isabel Dos Santos Silva
  • Nichola Johnson
  • Ruth Swann
  • Miriam Dwek
  • Katherine-Anne Perkins
  • Cheryl Gillett
  • Richard Houlston
  • Gillian Ross
  • Paolo De Ieso
  • Melissa C Southey
  • John L Hopper
  • Elena Provenzano
  • Carmel Apicella
  • Jelle Wesseling
  • Sten Cornelissen
  • Renske Keeman
  • Peter A Fasching
  • Sebastian M Jud
  • Arif B Ekici
  • Matthias W Beckmann
  • Michael J Kerin
  • Federick Marme
  • Andreas Schneeweiss
  • Christof Sohn
  • Barbara Burwinkel
  • Pascal Guénel
  • Therese Truong
  • Pierre Laurent-Puig
  • Pierre Kerbrat
  • Stig E Bojesen
  • Børge G Nordestgaard
  • Sune F Nielsen
  • Henrik Flyger
  • Roger L Milne
  • Jose Ignacio Arias Perez
  • Primitiva Menéndez
  • Javier Benitez
  • GENICA Network
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Invasive 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 = 6.0 × 10(-10); P-het for ILC vs IDC ER+ tumors = 1.8 × 10(-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.

OriginalsprogEngelsk
TidsskriftP L o S Genetics (Online)
Vol/bind10
Udgave nummer4
Sider (fra-til)e1004285
ISSN1553-7404
DOI
StatusUdgivet - apr. 2014

ID: 44381628