Genetic variation in stromal proteins decorin and lumican with breast cancer: investigations in two case-control studies

被引:40
作者
Kelemen, Linda E. [2 ]
Couch, Fergus J. [3 ]
Ahmed, Shahana [4 ]
Dunning, Alison M. [4 ]
Pharoah, Paul D. P. [4 ]
Easton, Douglas F. [4 ,5 ]
Fredericksen, Zachary S. [1 ]
Vierkant, Robert A. [1 ]
Pankratz, V. Shane [1 ]
Goode, Ellen L. [1 ]
Scott, Christopher G. [1 ]
Rider, David N. [1 ]
Wang, Xianshu [3 ]
Cerhan, James R. [4 ]
Vachon, Celine M. [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN 55905 USA
[2] Alberta Canc Board, Dept Populat Hlth Res, Calgary, AB T2N 4N2, Canada
[3] Mayo Clin, Coll Med, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[4] Univ Cambridge, Dept Oncol, Strangeways Res Lab, Canc Res UK, Cambridge CB1 8RN, England
[5] Univ Cambridge, Strangeways Res Lab, Dept Publ Hlth & Primary Care, Cambridge CB1 8RN, England
来源
BREAST CANCER RESEARCH | 2008年 / 10卷 / 06期
基金
美国国家卫生研究院;
关键词
D O I
10.1186/bcr2201
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction The stroma is the supportive framework of biologic tissue in the breast, consisting of various proteins such as the proteoglycans, decorin and lumican. Altered expression of decorin and lumican is associated with breast tumors. We hypothesized that genetic variation in the decorin (DCN) and lumican (LUM) genes may contribute to breast cancer. Methods We investigated associations of 14 common polymorphisms in the DCN and LUM genes with 798 breast cancer cases and 843 controls from Mayo Clinic, MN, USA. One polymorphism per gene with the strongest risk association in the Mayo Clinic sample was genotyped in 4,470 breast cancer cases and 4,560 controls from East Anglia, England (Studies of Epidemiology and Risk Factors in Cancer Heredity (SEARCH)). Results In the Mayo Clinic sample, six polymorphisms were associated with breast cancer risk (P-trend <= 0.05). The association with LUM rs2268578, evaluated further in SEARCH, was positive, although the odds ratios (OR) were weaker and not statistically significant. ORs were 1.4 (95% confidence interval [CI], 1.1 to 1.8) for heterozygotes and 2.2 (95% CI, 1.1 to 4.3; P-2 df = 0.002) for homozygotes in the Mayo Clinic sample, and were 1.1 (95% CI, 0.9 to 1.2) for heterozygotes and 1.4 (95% CI, 1.0 to 2.1; P-2 df = 0.13) for homozygotes in the SEARCH sample. In combined analyses, the ORs were 1.1 (95% CI, 1.0 to 1.2) for heterozygotes and 1.6 (95% CI, 1.2 to 2.3; P-2 df = 0.005) for homozygotes. Positive associations for this polymorphism were observed for estrogen receptor-positive tumors in both the Mayo Clinic sample (OR for heterozygotes = 1.5, 1.1 to 1.9 and OR for homozygotes = 2.5, 1.2 to 5.3; P-2 df = 0.001) and the SEARCH sample (OR for heterozygotes = 1.0, 0.9 to 1.1 and OR for homozygotes = 1.6, 1.0 to 2.5; P-2 df = 0.10). In combined analyses, the ORs were 1.1 (95% CI, 0.9 to 1.2) for heterozygotes and 1.9 (95% CI, 1.3 to 2.8; P-2 df = 0.001) for homozygotes. Conclusions Although LUM rs2268578 was associated with breast cancer in the Mayo Clinic study, particularly estrogen receptor-positive breast cancer, weaker and modest associations were observed in the SEARCH sample. These modest associations will require larger samples to adequately assess the importance of this polymorphism in breast cancer.
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