The University of Southampton
University of Southampton Institutional Repository

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy
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?9). Such survival-associated variants can represent ideal targets for tailored therapeutics, and may also enhance our current prognostic prediction capabilities
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Li, Jingmei
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Lindström, Linda S.
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Foo, Jia N.
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Li, Jingmei, Lindström, Linda S. and Foo, Jia N. et al. (2014) 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy. Nature Communications, 5, 4051-[9pp]. (doi:10.1038/ncomms5051).

Record type: Article

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?9). Such survival-associated variants can represent ideal targets for tailored therapeutics, and may also enhance our current prognostic prediction capabilities

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Accepted/In Press date: 6 May 2014
Published date: 17 June 2014
Organisations: Cancer Sciences, Clinical Trials Unit

Identifiers

Local EPrints ID: 382520
URI: http://eprints.soton.ac.uk/id/eprint/382520
PURE UUID: 76c582ee-9fee-4fe0-9f13-9fb9a1a0fba8
ORCID for William J. Tapper: ORCID iD orcid.org/0000-0002-5896-1889
ORCID for Diana M. Eccles: ORCID iD orcid.org/0000-0002-9935-3169

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Date deposited: 06 Oct 2015 14:01
Last modified: 15 Mar 2024 03:02

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Contributors

Author: Jingmei Li
Author: Linda S. Lindström
Author: Jia N. Foo
Author: Sajjad Rafiq
Author: Marjanka K. Schmidt
Author: Paul D. P. Pharoah
Author: Kyriaki Michailidou
Author: Joe Dennis
Author: Manjeet K. Bolla
Author: Qin Wang
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