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miRNA 基因单核苷酸多态性与乳腺癌风险和生存的关联:卡罗莱纳乳腺癌研究。

Association of germline microRNA SNPs in pre-miRNA flanking region and breast cancer risk and survival: the Carolina Breast Cancer Study.

机构信息

Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Cancer Causes Control. 2013 Jun;24(6):1099-109. doi: 10.1007/s10552-013-0187-z. Epub 2013 Mar 23.

Abstract

PURPOSE

Common germline variation in the 5' region proximal to precursor (pre-) miRNA gene sequences is evaluated for association with breast cancer risk and survival among African Americans and Caucasians.

METHODS

We genotyped nine single nucleotide polymorphisms (SNPs) within six miRNA gene regions previously associated with breast cancer, in 1,972 cases and 1,776 controls. In a race-stratified analysis using unconditional logistic regression, odds ratios (ORs) and 95 % confidence intervals (CIs) were calculated to evaluate SNP association with breast cancer risk. Additionally, hazard ratios (HRs) for breast cancer-specific mortality were estimated.

RESULTS

Two miR-185 SNPs provided suggestive evidence of an inverse association with breast cancer risk (rs2008591, OR = 0.72 (95 % CI = 0.53-0.98, p value = 0.04) and rs887205, OR = 0.71 (95 % CI = 0.52-0.96, p value = 0.03), respectively) among African Americans. Two SNPs, miR-34b/34c (rs4938723, HR = 0.57 (95 % CI = 0.37-0.89, p value = 0.01)) and miR-206 (rs6920648, HR = 0.77 (95 % CI = 0.61-0.97, p value = 0.02)), provided evidence of association with breast cancer survival. Further adjustment for stage resulted in more modest associations with survival (HR = 0.65 [95 % CI = 0.42-1.02, p value = 0.06] and HR = 0.79 [95 % CI = 0.62-1.00, p value = 0.05, respectively]).

CONCLUSIONS

Our results suggest that germline variation in the 5' region proximal to pre-miRNA gene sequences may be associated with breast cancer risk among African Americans and breast cancer-specific survival generally; however, further validation is needed to confirm these findings.

摘要

目的

评估前体(pre-)miRNA 基因序列近端 5' 区域常见的种系变异与非裔美国人和白种人乳腺癌风险和生存的关系。

方法

我们对先前与乳腺癌相关的六个 miRNA 基因区域内的 9 个单核苷酸多态性(SNP)进行了基因分型,共纳入 1972 例病例和 1776 例对照。采用非条件逻辑回归进行种族分层分析,计算 SNP 与乳腺癌风险的比值比(OR)和 95%置信区间(CI),以评估 SNP 与乳腺癌风险的关系。此外,还估计了乳腺癌特异性死亡率的风险比(HR)。

结果

两个 miR-185 SNP 提供了乳腺癌风险呈负相关的初步证据(rs2008591,OR=0.72(95%CI=0.53-0.98,p 值=0.04)和 rs887205,OR=0.71(95%CI=0.52-0.96,p 值=0.03))。两个 SNP,miR-34b/34c(rs4938723,HR=0.57(95%CI=0.37-0.89,p 值=0.01))和 miR-206(rs6920648,HR=0.77(95%CI=0.61-0.97,p 值=0.02)),为乳腺癌生存提供了关联证据。进一步调整分期后,与生存的关联更加适度(HR=0.65(95%CI=0.42-1.02,p 值=0.06)和 HR=0.79(95%CI=0.62-1.00,p 值=0.05))。

结论

我们的研究结果表明,pre-miRNA 基因序列近端 5' 区域的种系变异可能与非裔美国人的乳腺癌风险和乳腺癌特异性生存有关,但需要进一步验证以确认这些发现。

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本文引用的文献

1
Single nucleotide polymorphism in hsa-mir-196a-2 and breast cancer risk: a case control study.
Twin Res Hum Genet. 2011 Oct;14(5):417-21. doi: 10.1375/twin.14.5.417.
2
A functional polymorphism in the pre-miR-146a gene is associated with risk and prognosis in adult glioma.
J Neurooncol. 2011 Dec;105(3):639-46. doi: 10.1007/s11060-011-0634-1. Epub 2011 Jul 9.
5
Investigative role of pre-microRNAs in bladder cancer patients: a case-control study in North India.
DNA Cell Biol. 2011 Jun;30(6):401-6. doi: 10.1089/dna.2010.1159. Epub 2011 Feb 23.
6
Effect of microRNA-206 on cytoskeleton remodelling by downregulating Cdc42 in MDA-MB-231 cells.
Tumori. 2010 Sep-Oct;96(5):751-5. doi: 10.1177/030089161009600518.
8
miR-185 targets RhoA and Cdc42 expression and inhibits the proliferation potential of human colorectal cells.
Cancer Lett. 2011 Feb 28;301(2):151-60. doi: 10.1016/j.canlet.2010.11.009. Epub 2010 Dec 24.
9
Intrinsic breast tumor subtypes, race, and long-term survival in the Carolina Breast Cancer Study.
Clin Cancer Res. 2010 Dec 15;16(24):6100-10. doi: 10.1158/1078-0432.CCR-10-1533.
10
Genetic variants in MicroRNA biosynthesis pathways and binding sites modify ovarian cancer risk, survival, and treatment response.
Cancer Res. 2010 Dec 1;70(23):9765-76. doi: 10.1158/0008-5472.CAN-10-0130. Epub 2010 Nov 30.

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