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核心蛋白聚糖和光蛋白聚糖的基因变异与乳腺癌:两项病例对照研究

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

作者信息

Kelemen Linda E, Couch Fergus J, Ahmed Shahana, Dunning Alison M, Pharoah Paul D P, Easton Douglas F, Fredericksen Zachary S, Vierkant Robert A, Pankratz V Shane, Goode Ellen L, Scott Christopher G, Rider David N, Wang Xianshu, Cerhan James R, Vachon Celine M

机构信息

Department of Population Health Research, Alberta Cancer Board, 1331 29th Street NW, Calgary, AB T2N 4N2, Canada.

出版信息

Breast Cancer Res. 2008;10(6):R98. doi: 10.1186/bcr2201. Epub 2008 Nov 26.

Abstract

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 <or= 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; P2 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; P2 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; P2 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;P2 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; P2 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; P2 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.

摘要

引言

基质是乳腺生物组织的支持框架,由多种蛋白质组成,如蛋白聚糖、核心蛋白聚糖和光蛋白聚糖。核心蛋白聚糖和光蛋白聚糖的表达改变与乳腺肿瘤相关。我们推测核心蛋白聚糖(DCN)和光蛋白聚糖(LUM)基因的遗传变异可能与乳腺癌有关。

方法

我们研究了美国明尼苏达州梅奥诊所798例乳腺癌病例和843例对照中DCN和LUM基因的14个常见多态性的关联。在来自英国东安格利亚的4470例乳腺癌病例和4560例对照(癌症遗传流行病学和危险因素研究(SEARCH))中,对梅奥诊所样本中每个基因具有最强风险关联的一个多态性进行基因分型。

结果

在梅奥诊所样本中,6个多态性与乳腺癌风险相关(P趋势≤0.05)。在SEARCH中进一步评估的与LUM rs2268578的关联为阳性,尽管优势比(OR)较弱且无统计学意义。在梅奥诊所样本中,杂合子的OR为1.4(95%置信区间[CI],1.1至1.8),纯合子的OR为2.2(95%CI,1.1至4.3;P2自由度=0.002),在SEARCH样本中,杂合子的OR为1.1(95%CI,0.9至1.2),纯合子的OR为1.4(95%CI,1.0至2.1;P2自由度=0.13)。在联合分析中,杂合子的OR为1.1(95%CI,1.0至1.2),纯合子的OR为1.6(95%CI,1.2至2.3;P2自由度=0.005)。在梅奥诊所样本(杂合子的OR=1.5,1.1至1.9;纯合子的OR=2.5,1.2至5.3;P2自由度=0.001)和SEARCH样本(杂合子的OR=1.0,0.9至1.1;纯合子的OR=1.6,1.0至2.5;P2自由度=0.10)中,雌激素受体阳性肿瘤均观察到该多态性的正相关。在联合分析中,杂合子的OR为1.1(95%CI,0.9至1.2),纯合子的OR为1.9(95%CI,1.3至2.8;P2自由度=0.001)。

结论

尽管在梅奥诊所研究中LUM rs2268578与乳腺癌相关,尤其是雌激素受体阳性乳腺癌,但在SEARCH样本中观察到的关联较弱且适度。这些适度的关联需要更大的样本量来充分评估该多态性在乳腺癌中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea5/2656894/b5ccce13ed98/bcr2201-1.jpg

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