Association of NCOA3 polymorphisms with breast cancer risk

被引:42
作者
Burwinkel, B
Wirtenberger, M
Klaes, R
Schmutzler, RK
Grzybowska, E
Försti, A
Frank, B
Bermejo, JL
Bugert, P
Wappenschmidt, B
Butkiewicz, D
Pamula, J
Pekala, W
Zientek, H
Mielzynska, D
Siwinska, E
Bartram, CR
Hemminki, K
机构
[1] German Canc Res Ctr, Div Mol Genet Epidemiol C050, D-69120 Heidelberg, Germany
[2] Heidelberg Univ, Inst Human Genet, Heidelberg, Germany
[3] Univ Cologne, Ctr Clin, Div Obstet & Gynecol, Dept Mol Gynaecooncol, Cologne, Germany
[4] Maria Sklodowska Curie Inst, Ctr Oncol, Dept Tumor Biol, Gliwice, Poland
[5] Inst Occupat Med & Environm Hlth, Dept Genet Toxicol, Sosnowiec, Poland
[6] Heidelberg Univ, Fac Clin Med, D-6800 Mannheim, Germany
[7] Karolinska Inst, Dept Biosci, Novum, Huddinge, Sweden
关键词
D O I
10.1158/1078-0432.CCR-04-1621
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The nuclear receptor coactivator 3 (NCOA3, also known as AIB1) is a coactivator of nuclear receptors like the estrogen receptor. NCOA3 is overexpressed in similar to 60% of primary human breast tumors, and high levels of NCOA3 expression are associated with tamoxifen resistance and worse survival rate. In contrast, NCOA3 deficiency suppresses nu w-Ha-ras - induced breast cancer initiation and progression in mice. Here, we analyzed the influence of NCOA3 coding single nucleotide polymorphisms on breast cancer risk by performing a case-control study using a German and a Polish study population and identified an association between NCOA3 polymorphisms and breast cancer. A joint analysis of the German and the Polish study population revealed a significant protective effect for the 1758G > C (Q586H) and 2880A > G (T960T) variants. In addition, haplotype analysis showed a protective effect of the 1758C-2880A and 1758G-2880G haplotypes (odds ratio 0.79; 95% confidence interval, 0.67-0.93; P = 0.004). Because of the impact of NCOA3 in antiestrogen therapy resistance, these polymorphisms might also influence therapy outcome in breast cancer.
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收藏
页码:2169 / 2174
页数:6
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