Abstract
Large population-based registry studies have shown that breast cancer prognosis is inherited. Here we analyse single-nucleotide polymorphisms (SNPs) of genes implicated in human immunology and inflammation as candidates for prognostic markers of breast cancer survival involving 1,804 oestrogen receptor (ER)-negative patients treated with chemotherapy (279 events) from 14 European studies in a prior large-scale genotyping experiment, which is part of the Collaborative Oncological Gene-environment Study (COGS) initiative. We carry out replication using Asian COGS samples (n=522, 53 events) and the Prospective Study of Outcomes in Sporadic versus Hereditary breast cancer (POSH) study (n=315, 108 events). Rs4458204-A near CCL20 (2q36.3) is found to be associated with breast cancer-specific death at a genome-wide significant level (n=2,641, 440 events, combined allelic hazard ratio (HR)=1.81 (1.49-2.19); P for trend=1.90 × 10 â ̂'9). Such survival-associated variants can represent ideal targets for tailored therapeutics, and may also enhance our current prognostic prediction capabilities.
Original language | English |
---|---|
Article number | 4051 |
Journal | Nature Communications |
Volume | 5 |
DOIs | |
Publication status | Published - 17 Jun 2014 |
Externally published | Yes |
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In: Nature Communications, Vol. 5, 4051, 17.06.2014.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
AU - Li, Jingmei
AU - Lindström, Linda S.
AU - Foo, Jia N.
AU - Rafiq, Sajjad
AU - Schmidt, Marjanka K.
AU - Pharoah, Paul D.P.
AU - Michailidou, Kyriaki
AU - Dennis, Joe
AU - Bolla, Manjeet K.
AU - Wang, Qin
AU - Van'T Veer, Laura J.
AU - Cornelissen, Sten
AU - Rutgers, Emiel
AU - Southey, Melissa C.
AU - Apicella, Carmel
AU - Dite, Gillian S.
AU - Hopper, John L.
AU - Fasching, Peter A.
AU - Haeberle, Lothar
AU - Ekici, Arif B.
AU - Beckmann, Matthias W.
AU - Blomqvist, Carl
AU - Muranen, Taru A.
AU - Aittomäki, Kristiina
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 - Investigators, Kconfab
AU - Phillips, Kelly Anne
AU - McLachlan, Sue Anne
AU - Lambrechts, Diether
AU - Thienpont, Bernard
AU - Smeets, Ann
AU - Wildiers, Hans
AU - Chang-Claude, Jenny
AU - Flesch-Janys, Dieter
AU - Seibold, Petra
AU - Rudolph, Anja
AU - Giles, Graham G.
AU - Baglietto, Laura
AU - Severi, Gianluca
AU - Haiman, Christopher A.
AU - Henderson, Brian E.
AU - Schumacher, Fredrick
AU - Le Marchand, Loic
AU - Kristensen, Vessela
AU - Alnæs, Grethe I.Grenaker
AU - Borresen-Dale, Anne Lise
AU - Nord, Silje
AU - Winqvist, Robert
AU - Pylkäs, Katri
AU - Jukkola-Vuorinen, Arja
AU - Grip, Mervi
AU - Andrulis, Irene L.
AU - Knight, Julia A.
AU - Glendon, Gord
AU - Tchatchou, Sandrine
AU - Devilee, Peter
AU - Tollenaar, Robert
AU - Seynaeve, Caroline
AU - Hooning, Maartje
AU - Kriege, Mieke
AU - Hollestelle, Antoinette
AU - Van Den Ouweland, Ans
AU - Li, Yi
AU - Hamann, Ute
AU - Torres, Diana
AU - Ulmer, Hans U.
AU - Rüdiger, Thomas
AU - Shen, Chen Yang
AU - Hsiung, Chia Ni
AU - Wu, Pei Ei
AU - Chen, Shou Tung
AU - Teo, Soo Hwang
AU - Taib, Nur Aishah Mohd
AU - Har Yip, Cheng
AU - Fuang Ho, Gwo
AU - Matsuo, Keitaro
AU - Ito, Hidemi
AU - Iwata, Hiroji
AU - Tajima, Kazuo
AU - Kang, Daehee
AU - Choi, Ji Yeob
AU - Park, Sue K.
AU - Yoo, Keun Young
AU - Maishman, Tom
AU - Tapper, William J.
AU - Dunning, Alison
AU - Shah, Mitul
AU - Luben, Robert
AU - Brown, Judith
AU - Chuen Khor, Chiea
AU - Eccles, Diana M.
AU - Nevanlinna, Heli
AU - Easton, Douglas
AU - Humphreys, Keith
AU - Liu, Jianjun
AU - Hall, Per
AU - Czene, Kamila
PY - 2014/6/17
Y1 - 2014/6/17
N2 - Large population-based registry studies have shown that breast cancer prognosis is inherited. Here we analyse single-nucleotide polymorphisms (SNPs) of genes implicated in human immunology and inflammation as candidates for prognostic markers of breast cancer survival involving 1,804 oestrogen receptor (ER)-negative patients treated with chemotherapy (279 events) from 14 European studies in a prior large-scale genotyping experiment, which is part of the Collaborative Oncological Gene-environment Study (COGS) initiative. We carry out replication using Asian COGS samples (n=522, 53 events) and the Prospective Study of Outcomes in Sporadic versus Hereditary breast cancer (POSH) study (n=315, 108 events). Rs4458204-A near CCL20 (2q36.3) is found to be associated with breast cancer-specific death at a genome-wide significant level (n=2,641, 440 events, combined allelic hazard ratio (HR)=1.81 (1.49-2.19); P for trend=1.90 × 10 â ̂'9). Such survival-associated variants can represent ideal targets for tailored therapeutics, and may also enhance our current prognostic prediction capabilities.
AB - Large population-based registry studies have shown that breast cancer prognosis is inherited. Here we analyse single-nucleotide polymorphisms (SNPs) of genes implicated in human immunology and inflammation as candidates for prognostic markers of breast cancer survival involving 1,804 oestrogen receptor (ER)-negative patients treated with chemotherapy (279 events) from 14 European studies in a prior large-scale genotyping experiment, which is part of the Collaborative Oncological Gene-environment Study (COGS) initiative. We carry out replication using Asian COGS samples (n=522, 53 events) and the Prospective Study of Outcomes in Sporadic versus Hereditary breast cancer (POSH) study (n=315, 108 events). Rs4458204-A near CCL20 (2q36.3) is found to be associated with breast cancer-specific death at a genome-wide significant level (n=2,641, 440 events, combined allelic hazard ratio (HR)=1.81 (1.49-2.19); P for trend=1.90 × 10 â ̂'9). Such survival-associated variants can represent ideal targets for tailored therapeutics, and may also enhance our current prognostic prediction capabilities.
UR - http://www.scopus.com/inward/record.url?scp=84902763179&partnerID=8YFLogxK
U2 - 10.1038/ncomms5051
DO - 10.1038/ncomms5051
M3 - Article
C2 - 24937182
AN - SCOPUS:84902763179
SN - 2041-1723
VL - 5
JO - Nature Communications
JF - Nature Communications
M1 - 4051
ER -