Résumé
Background: Our recent genome-wide association study identified a novel breast cancer susceptibility locus at 9q31.2 (rs865686). Methods: To further investigate the rs865686-breast cancer association, we conducted a replication study within the Breast Cancer Association Consortium, which comprises 37 case-control studies (48,394 cases, 50,836 controls). Results: This replication study provides additional strong evidence of an inverse association between rs865686 and breast cancer risk [study-adjusted per G-allele OR, 0.90; 95% confidence interval (CI), 0.88; 0.91, P =2.01 × 10-29] among women of European ancestry. There were ethnic differences in the estimated minor (G)-allele frequency among controls [0.09, 0.30, and 0.38 among, respectively, Asians, Eastern Europeans, and other Europeans; P for heterogeneity (Phet) = 1.3 × 10-143], but no evidence of ethnic differences in per allele OR (Phet = 0.43). rs865686 was associated with estrogen receptor-positive (ER+) disease (per G-allele OR, 0.89; 95% CI, 0.86-0.91; P = 3.13 × 10-22) but less strongly, if at all, with ER-negative (ER+) disease (OR, 0.98; 95% CI, 0.94-1.02; P = 0.26; Phet = 1.16 × 10-6), with no evidence of independent heterogeneity by progesterone receptor or HER2 status. The strength of the breast cancer association decreased with increasing age at diagnosis, with case-only analysis showing a trend in the number of copies of theGallele with increasing age at diagnosis (P for linear trend = 0.0095), but only among women with ER+ tumors. Conclusions: This study is the first to show that rs865686 is a susceptibility marker for ER+ breast cancer. Impact: The findings further support the view that genetic susceptibility varies according to tumor subtype.
langue originale | Anglais |
---|---|
Pages (de - à) | 1783-1791 |
Nombre de pages | 9 |
journal | Cancer Epidemiology Biomarkers and Prevention |
Volume | 21 |
Numéro de publication | 10 |
Les DOIs | |
état | Publié - 1 janv. 2012 |
Modification externe | Oui |
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Dans: Cancer Epidemiology Biomarkers and Prevention, Vol 21, Numéro 10, 01.01.2012, p. 1783-1791.
Résultats de recherche: Contribution à un journal › Article › Revue par des pairs
TY - JOUR
T1 - 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer
T2 - Evidence from the Breast Cancer Association Consortium
AU - Warren, Helen
AU - Dudbridge, Frank
AU - Fletcher, Olivia
AU - Orr, Nick
AU - Johnson, Nichola
AU - Hopper, John L.
AU - Apicella, Carmel
AU - Southey, Melissa C.
AU - Mahmoodi, Maryam
AU - Schmidt, Marjanka K.
AU - Broeks, Annegien
AU - Cornelissen, Sten
AU - Braaf, Linda M.
AU - Muir, Kenneth R.
AU - Lophatananon, Artitaya
AU - Chaiwerawattana, Arkom
AU - Wiangnon, Surapon
AU - Fasching, Peter A.
AU - Beckmann, Matthias W.
AU - Ekici, Arif B.
AU - Schulz-Wendtland, Ruediger
AU - Sawyer, Elinor J.
AU - Tomlinson, Ian
AU - Kerin, Michael
AU - Burwinkel, Barbara
AU - Marme, Frederik
AU - Schneeweiss, Andreas
AU - Sohn, Christof
AU - Guénel, Pascal
AU - Truong, Thérèse
AU - Laurent-Puig, Pierre
AU - Mulot, Claire
AU - Bojesen, Stig E.
AU - Nielsen, Sune F.
AU - Flyger, Henrik
AU - Nordestgaard, Børge G.
AU - Milne, Roger L.
AU - Benítez, Javier
AU - Arias-Pérez, José Ignacio
AU - Zamora, M. Pilar
AU - Anton-Culver, Hoda
AU - Ziogas, Argyrios
AU - Bernstein, Leslie
AU - Dur, Christina Clarke
AU - Brenner, Hermann
AU - Müller, Heiko
AU - Arndt, Volker
AU - Langheinz, Anne
AU - Meindl, Alfons
AU - Golatta, Michael
AU - Bartram, Claus R.
AU - Schmutzler, Rita K.
AU - Brauch, Hiltrud
AU - Justenhoven, Christina
AU - Brüning, Thomas
AU - Chang-Claude, Jenny
AU - Wang-Gohrke, Shan
AU - Eilber, Ursula
AU - Dörk, Thilo
AU - Schürmann, Peter
AU - Bremer, Michael
AU - Hillemanns, Peter
AU - Nevanlinna, Heli
AU - Muranen, Taru A.
AU - Aittomäki, Kristiina
AU - Blomqvist, Carl
AU - Bogdanova, Natalia
AU - Antonenkova, Natalia
AU - Rogov, Yuriy
AU - Bermisheva, Marina
AU - Prokofyeva, Darya
AU - Zinnatullina, Guzel
AU - Khusnutdinova, Elza
AU - Lindblom, Annika
AU - Margolin, Sara
AU - Mannermaa, Arto
AU - Kosma, Veli Matti
AU - Hartikainen, Jaana M.
AU - Kataja, Vesa
AU - Chenevix-Trench, Georgia
AU - Beesley, Jonathan
AU - Chen, Xiaoqing
AU - Lambrechts, Diether
AU - Smeets, Ann
AU - Paridaens, Robert
AU - Weltens, Caroline
AU - Flesch-Janys, Dieter
AU - Buck, Katharina
AU - Behrens, Sabine
AU - Peterlongo, Paolo
AU - Bernard, Loris
AU - Manoukian, Siranoush
AU - Radice, Paolo
AU - Couch, Fergus J.
AU - Vachon, Celine
AU - Wang, Xianshu
AU - Olson, Janet
AU - Giles, Graham
AU - Baglietto, Laura
AU - McLean, Cariona A.
AU - Severi, Gianluca
AU - John, Esther M.
AU - Miron, Alexander
AU - Winqvist, Robert
AU - Pylkäs, Katri
AU - Jukkola-Vuorinen, Arja
AU - Grip, Mervi
AU - Andrulis, Irene L.
AU - Knight, Julia A.
AU - Mulligan, Anna Marie
AU - Weerasooriya, Nayana
AU - Devilee, Peter
AU - Tollenaar, Robert A.E.M.
AU - Martens, John W.M.
AU - Seynaeve, Caroline M.
AU - Hooning, Maartje J.
AU - Hollestelle, Antoinette
AU - Jager, Agnes
AU - Tilanus-Linthorst, Madeleine M.A.
AU - Hall, Per
AU - Czene, Kamila
AU - Liu, Jianjun
AU - Li, Jingmei
AU - Cox, Angela
AU - Cross, Simon S.
AU - Brock, Ian W.
AU - Reed, Malcolm W.R.
AU - Pharoah, Paul
AU - Blows, Fiona M.
AU - Dunning, Alison M.
AU - Ghoussaini, Maya
AU - Ashworth, Alan
AU - Swerdlow, Anthony
AU - Jones, Michael
AU - Schoemaker, Minouk
AU - Easton, Douglas F.
AU - Humphreys, Manjeet
AU - Wang, Qin
AU - Peto, Julian
AU - Dos-Santos-Silva, Isabel
PY - 2012/1/1
Y1 - 2012/1/1
N2 - Background: Our recent genome-wide association study identified a novel breast cancer susceptibility locus at 9q31.2 (rs865686). Methods: To further investigate the rs865686-breast cancer association, we conducted a replication study within the Breast Cancer Association Consortium, which comprises 37 case-control studies (48,394 cases, 50,836 controls). Results: This replication study provides additional strong evidence of an inverse association between rs865686 and breast cancer risk [study-adjusted per G-allele OR, 0.90; 95% confidence interval (CI), 0.88; 0.91, P =2.01 × 10-29] among women of European ancestry. There were ethnic differences in the estimated minor (G)-allele frequency among controls [0.09, 0.30, and 0.38 among, respectively, Asians, Eastern Europeans, and other Europeans; P for heterogeneity (Phet) = 1.3 × 10-143], but no evidence of ethnic differences in per allele OR (Phet = 0.43). rs865686 was associated with estrogen receptor-positive (ER+) disease (per G-allele OR, 0.89; 95% CI, 0.86-0.91; P = 3.13 × 10-22) but less strongly, if at all, with ER-negative (ER+) disease (OR, 0.98; 95% CI, 0.94-1.02; P = 0.26; Phet = 1.16 × 10-6), with no evidence of independent heterogeneity by progesterone receptor or HER2 status. The strength of the breast cancer association decreased with increasing age at diagnosis, with case-only analysis showing a trend in the number of copies of theGallele with increasing age at diagnosis (P for linear trend = 0.0095), but only among women with ER+ tumors. Conclusions: This study is the first to show that rs865686 is a susceptibility marker for ER+ breast cancer. Impact: The findings further support the view that genetic susceptibility varies according to tumor subtype.
AB - Background: Our recent genome-wide association study identified a novel breast cancer susceptibility locus at 9q31.2 (rs865686). Methods: To further investigate the rs865686-breast cancer association, we conducted a replication study within the Breast Cancer Association Consortium, which comprises 37 case-control studies (48,394 cases, 50,836 controls). Results: This replication study provides additional strong evidence of an inverse association between rs865686 and breast cancer risk [study-adjusted per G-allele OR, 0.90; 95% confidence interval (CI), 0.88; 0.91, P =2.01 × 10-29] among women of European ancestry. There were ethnic differences in the estimated minor (G)-allele frequency among controls [0.09, 0.30, and 0.38 among, respectively, Asians, Eastern Europeans, and other Europeans; P for heterogeneity (Phet) = 1.3 × 10-143], but no evidence of ethnic differences in per allele OR (Phet = 0.43). rs865686 was associated with estrogen receptor-positive (ER+) disease (per G-allele OR, 0.89; 95% CI, 0.86-0.91; P = 3.13 × 10-22) but less strongly, if at all, with ER-negative (ER+) disease (OR, 0.98; 95% CI, 0.94-1.02; P = 0.26; Phet = 1.16 × 10-6), with no evidence of independent heterogeneity by progesterone receptor or HER2 status. The strength of the breast cancer association decreased with increasing age at diagnosis, with case-only analysis showing a trend in the number of copies of theGallele with increasing age at diagnosis (P for linear trend = 0.0095), but only among women with ER+ tumors. Conclusions: This study is the first to show that rs865686 is a susceptibility marker for ER+ breast cancer. Impact: The findings further support the view that genetic susceptibility varies according to tumor subtype.
UR - http://www.scopus.com/inward/record.url?scp=84867322171&partnerID=8YFLogxK
U2 - 10.1158/1055-9965.EPI-12-0526
DO - 10.1158/1055-9965.EPI-12-0526
M3 - Article
C2 - 22859399
AN - SCOPUS:84867322171
SN - 1055-9965
VL - 21
SP - 1783
EP - 1791
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 10
ER -