Résumé
Background: The single-nucleotide polymorphism (SNP) 5p12-rs10941679 has been found to be associated with risk of breast cancer, particularly estrogen receptor (ER)-positive disease. We aimed to further explore this association overall, and by tumor histopathology, in the Breast Cancer Association Consortium. Methods: Data were combined from 37 studies, including 40,972 invasive cases, 1,398 cases of ductal carcinoma in situ (DCIS), and 46,334 controls, all of white European ancestry, as well as 3,007 invasive cases and 2,337 controls of Asian ancestry. Associations overall and by tumor invasiveness and histopathology were assessed using logistic regression. Results: For white Europeans, the per-allele OR associated with 5p12-rs10941679 was 1.11 (95% CI = 1.08-1.14, P = 7 × 10-18) for invasive breast cancer and 1.10 (95% CI = 1.01-1.21, P = 0.03) for DCIS. For Asian women, the estimated OR for invasive disease was similar (OR = 1.07, 95%CI = 0.99-1.15, P = 0.09). Further analyses suggested that the association in white Europeans was largely limited to progesterone receptor (PR)- positive disease (per-allele OR = 1.16, 95% CI = 1.12-1.20, P = 1 × 10-18 vs. OR = 1.03, 95% CI = 0.99-1.07, P = 0.2 for PR-negative disease; Pheterogeneity = 2 × 10 -7); heterogeneity by ER status was not observed (P= 0.2) once PR status was accounted for. The association was also stronger for lower grade tumors [per-allele OR (95% CI) = 1.20 (1.14-1.25), 1.13 (1.09-1.16), and 1.04 (0.99-1.08) for grade 1, 2, and 3/4, respectively; Ptrend = 5 × 10 -7]. Conclusion: 5p12 is a breast cancer susceptibility locus for PR-positive, lower grade breast cancer. Impact: Multicenter fine-mapping studies of this region are needed as a first step to identifying the causal variant or variants.
langue originale | Anglais |
---|---|
Pages (de - à) | 2222-2231 |
Nombre de pages | 10 |
journal | Cancer Epidemiology Biomarkers and Prevention |
Volume | 20 |
Numéro de publication | 10 |
Les DOIs | |
état | Publié - 1 janv. 2011 |
Modification externe | Oui |
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Dans: Cancer Epidemiology Biomarkers and Prevention, Vol 20, Numéro 10, 01.01.2011, p. 2222-2231.
Résultats de recherche: Contribution à un journal › Article › Revue par des pairs
TY - JOUR
T1 - Confirmation of 5p12 as a susceptibility locus for progesterone-receptor- positive, lower grade breast cancer
AU - Milne, Roger L.
AU - Goode, Ellen L.
AU - García-Closas, Montserrat
AU - Couch, Fergus J.
AU - Severi, Gianluca
AU - Hein, Rebecca
AU - Fredericksen, Zachary
AU - Malats, Núria
AU - Zamora, M. Pilar
AU - Pérez, Jose Ignacio Arias
AU - Benítez, Javier
AU - Dörk, Thilo
AU - Schürmann, Peter
AU - Karstens, Johann H.
AU - Hillemanns, Peter
AU - Cox, Angela
AU - Brock, Ian W.
AU - Elliot, Graeme
AU - Cross, Simon S.
AU - Seal, Sheila
AU - Turnbull, Clare
AU - Renwick, Anthony
AU - Rahman, Nazneen
AU - Shen, Chen Yang
AU - Yu, Jyh Cherng
AU - Huang, Chiun Sheng
AU - Hou, Ming Feng
AU - Nordestgaard, Børge G.
AU - Bojesen, Stig E.
AU - Lanng, Charlotte
AU - Alnæs, Grethe Grenaker
AU - Kristensen, Vessela
AU - Børrensen-Dale, Anne Lise
AU - Hopper, John L.
AU - Dite, Gillian S.
AU - Apicella, Carmel
AU - Southey, Melissa C.
AU - Lambrechts, Diether
AU - Yesilyurt, Betül T.
AU - Floris, Giuseppe
AU - Leunen, Karin
AU - Sangrajrang, Suleeporn
AU - Gaborieau, Valerie
AU - Brennan, Paul
AU - McKay, James
AU - Chang-Claude, Jenny
AU - Wang-Gohrke, Shan
AU - Radice, Paolo
AU - Peterlongo, Paolo
AU - Manoukian, Siranoush
AU - Barile, Monica
AU - Giles, Graham G.
AU - Baglietto, Laura
AU - John, Esther M.
AU - Miron, Alexander
AU - Chanock, Stephen J.
AU - Lissowska, Jolanta
AU - Sherman, Mark E.
AU - Figueroa, Jonine D.
AU - Bogdanova, Natalia V.
AU - Antonenkova, Natalia N.
AU - Zalutsky, Iosif V.
AU - Rogov, Yuri I.
AU - Fasching, Peter A.
AU - Bayer, Christian M.
AU - Ekici, Arif B.
AU - Beckmann, Matthias W.
AU - Brenner, Hermann
AU - Müller, Heiko
AU - Arndt, Volker
AU - Stegmaier, Christa
AU - Andrulis, Irene L.
AU - Knight, Julia A.
AU - Glendon, Gord
AU - Mulligan, Anna Marie
AU - Mannermaa, Arto
AU - Kataja, Vesa
AU - Kosma, Veli Matti
AU - Hartikainen, Jaana M.
AU - Meindl, Alfons
AU - Heil, Joerg
AU - Bartram, Claus R.
AU - Schmutzler, Rita K.
AU - Thomas, Gilles D.
AU - Hoover, Robert N.
AU - Fletcher, Olivia
AU - Gibson, Lorna J.
AU - Dos Santos Silva, Isabel
AU - Peto, Julian
AU - Nickels, Stefan
AU - Flesch-Janys, Dieter
AU - Anton-Culver, Hoda
AU - Ziogas, Argyrios
AU - Sawyer, Elinor
AU - Tomlinson, Ian
AU - Kerin, Michael
AU - Miller, Nicola
AU - Schmidt, Marjanka K.
AU - Broeks, Annegien
AU - Van't Veer, Laura J.
AU - Tollenaar, Rob A.E.M.
AU - Pharoah, Paul D.P.
AU - Dunning, Alison M.
AU - Pooley, Karen A.
AU - Marme, Frederik
AU - Schneeweiss, Andreas
AU - Sohn, Christof
AU - Burwinkel, Barbara
AU - Jakubowska, Anna
AU - Lubinski, Jan
AU - Jaworska, Katarzyna
AU - Durda, Katarzyna
AU - Kang, Daehee
AU - Yoo, Keun Young
AU - Noh, Dong Young
AU - Ahn, Sei Hyun
AU - Hunter, David J.
AU - Hankinson, Susan E.
AU - Kraft, Peter
AU - Lindstrom, Sara
AU - Chen, Xiaoqing
AU - Beesley, Jonathan
AU - Hamann, Ute
AU - Harth, Volker
AU - Justenhoven, Christina
AU - Winqvist, Robert
AU - Pylkäs, Katri
AU - Jukkola-Vuorinen, Arja
AU - Grip, Mervi
AU - Hooning, Maartje
AU - Hollestelle, Antoinette
AU - Oldenburg, Rogier A.
AU - Tilanus-Linthorst, Madeleine
AU - Khusnutdinova, Elza
AU - Bermisheva, Marina
AU - Prokofieva, Darya
AU - Farahtdinova, Albina
AU - Olson, Janet E.
AU - Wang, Xianshu
AU - Humphreys, Manjeet K.
AU - Wang, Qin
AU - Chenevix-Trench, Georgia
AU - Easton, Douglas F.
PY - 2011/1/1
Y1 - 2011/1/1
N2 - Background: The single-nucleotide polymorphism (SNP) 5p12-rs10941679 has been found to be associated with risk of breast cancer, particularly estrogen receptor (ER)-positive disease. We aimed to further explore this association overall, and by tumor histopathology, in the Breast Cancer Association Consortium. Methods: Data were combined from 37 studies, including 40,972 invasive cases, 1,398 cases of ductal carcinoma in situ (DCIS), and 46,334 controls, all of white European ancestry, as well as 3,007 invasive cases and 2,337 controls of Asian ancestry. Associations overall and by tumor invasiveness and histopathology were assessed using logistic regression. Results: For white Europeans, the per-allele OR associated with 5p12-rs10941679 was 1.11 (95% CI = 1.08-1.14, P = 7 × 10-18) for invasive breast cancer and 1.10 (95% CI = 1.01-1.21, P = 0.03) for DCIS. For Asian women, the estimated OR for invasive disease was similar (OR = 1.07, 95%CI = 0.99-1.15, P = 0.09). Further analyses suggested that the association in white Europeans was largely limited to progesterone receptor (PR)- positive disease (per-allele OR = 1.16, 95% CI = 1.12-1.20, P = 1 × 10-18 vs. OR = 1.03, 95% CI = 0.99-1.07, P = 0.2 for PR-negative disease; Pheterogeneity = 2 × 10 -7); heterogeneity by ER status was not observed (P= 0.2) once PR status was accounted for. The association was also stronger for lower grade tumors [per-allele OR (95% CI) = 1.20 (1.14-1.25), 1.13 (1.09-1.16), and 1.04 (0.99-1.08) for grade 1, 2, and 3/4, respectively; Ptrend = 5 × 10 -7]. Conclusion: 5p12 is a breast cancer susceptibility locus for PR-positive, lower grade breast cancer. Impact: Multicenter fine-mapping studies of this region are needed as a first step to identifying the causal variant or variants.
AB - Background: The single-nucleotide polymorphism (SNP) 5p12-rs10941679 has been found to be associated with risk of breast cancer, particularly estrogen receptor (ER)-positive disease. We aimed to further explore this association overall, and by tumor histopathology, in the Breast Cancer Association Consortium. Methods: Data were combined from 37 studies, including 40,972 invasive cases, 1,398 cases of ductal carcinoma in situ (DCIS), and 46,334 controls, all of white European ancestry, as well as 3,007 invasive cases and 2,337 controls of Asian ancestry. Associations overall and by tumor invasiveness and histopathology were assessed using logistic regression. Results: For white Europeans, the per-allele OR associated with 5p12-rs10941679 was 1.11 (95% CI = 1.08-1.14, P = 7 × 10-18) for invasive breast cancer and 1.10 (95% CI = 1.01-1.21, P = 0.03) for DCIS. For Asian women, the estimated OR for invasive disease was similar (OR = 1.07, 95%CI = 0.99-1.15, P = 0.09). Further analyses suggested that the association in white Europeans was largely limited to progesterone receptor (PR)- positive disease (per-allele OR = 1.16, 95% CI = 1.12-1.20, P = 1 × 10-18 vs. OR = 1.03, 95% CI = 0.99-1.07, P = 0.2 for PR-negative disease; Pheterogeneity = 2 × 10 -7); heterogeneity by ER status was not observed (P= 0.2) once PR status was accounted for. The association was also stronger for lower grade tumors [per-allele OR (95% CI) = 1.20 (1.14-1.25), 1.13 (1.09-1.16), and 1.04 (0.99-1.08) for grade 1, 2, and 3/4, respectively; Ptrend = 5 × 10 -7]. Conclusion: 5p12 is a breast cancer susceptibility locus for PR-positive, lower grade breast cancer. Impact: Multicenter fine-mapping studies of this region are needed as a first step to identifying the causal variant or variants.
UR - http://www.scopus.com/inward/record.url?scp=80053517824&partnerID=8YFLogxK
U2 - 10.1158/1055-9965.EPI-11-0569
DO - 10.1158/1055-9965.EPI-11-0569
M3 - Article
AN - SCOPUS:80053517824
SN - 1055-9965
VL - 20
SP - 2222
EP - 2231
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 10
ER -