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尼美根断裂综合征1基因657del5多态性与乳腺癌风险之间的显著关联。

Significant association between Nijmegen breakage syndrome 1 657del5 polymorphism and breast cancer risk.

作者信息

Zhang Guofeng, Zeng Yu, Liu Zhongyan, Wei Weiwei

机构信息

Department of General Surgery, Tongji Hospital, Tongji University School of Medicine, Shanghai, 200065, China,

出版信息

Tumour Biol. 2013 Oct;34(5):2753-7. doi: 10.1007/s13277-013-0830-z. Epub 2013 Jun 14.

DOI:10.1007/s13277-013-0830-z
PMID:23765759
Abstract

Many studies were published to evaluate the association between Nijmegen breakage syndrome 1 (NBS1) 657del5 polymorphism and breast cancer risk, but the results remained inconsistent. To derive a more precise estimation on the possible association, we performed a meta-analysis of previous published studies. Case-control studies on the association between NBS1 657del5 polymorphisms and breast cancer risk were included into this meta-analysis. We used the odds ratio (OR) with 95 % confidence interval (95 % CI) to assess the strength of the association. Ten studies with a total of 25,365 subjects were identified and included into this meta-analysis. Meta-analysis of those ten studies showed that there was a significant association between NBS1 657del5 polymorphisms and breast cancer risk (pooled OR = 2.66, 95 % CI 1.82-3.90, P < 0.001). The cumulative meta-analyses showed a trend of a more significant association between NBS1 657del5 polymorphisms and breast cancer risk as data accumulated by publication year. Thus, our meta-analysis suggests that there was a significant association between NBS1 657del5 polymorphisms and breast cancer risk, and NBS1 657del5 polymorphism results in an increased risk of breast cancer.

摘要

许多研究已发表,旨在评估尼美根断裂综合征1(NBS1)657del5多态性与乳腺癌风险之间的关联,但结果仍不一致。为了对可能的关联进行更精确的估计,我们对先前发表的研究进行了荟萃分析。关于NBS1 657del5多态性与乳腺癌风险之间关联的病例对照研究被纳入本荟萃分析。我们使用比值比(OR)及95%置信区间(95%CI)来评估关联强度。共识别出10项研究,涉及25365名受试者,并将其纳入本荟萃分析。对这10项研究的荟萃分析表明,NBS1 657del5多态性与乳腺癌风险之间存在显著关联(合并OR = 2.66,95%CI 1.82 - 3.90,P < 0.001)。累积荟萃分析显示,随着按发表年份积累的数据增多,NBS1 657del5多态性与乳腺癌风险之间的关联有更显著的趋势。因此,我们的荟萃分析表明,NBS1 657del5多态性与乳腺癌风险之间存在显著关联,且NBS1 657del5多态性会导致乳腺癌风险增加。

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1
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Mutat Res. 2012 Oct-Dec;751(2):158-246. doi: 10.1016/j.mrrev.2012.06.002. Epub 2012 Jun 26.
2
Germline mutations 657del5 and 643C>T (R215W) in NBN are not likely to be associated with increased risk of breast cancer in Czech women.
Breast Cancer Res Treat. 2012 Jun;133(2):809-11. doi: 10.1007/s10549-012-2049-x. Epub 2012 Apr 11.
3
Gene expression profiling in breast cancer: classification, prognostication, and prediction.乳腺癌的基因表达谱分析:分类、预后和预测。
俄罗斯中部人群中参与多基因检测的乳腺癌患者和健康供体的高风险和中度风险变异
Int J Mol Sci. 2024 Nov 25;25(23):12640. doi: 10.3390/ijms252312640.
4
Impact of Molecular Profiling on Therapy Management in Breast Cancer.分子谱分析对乳腺癌治疗管理的影响
J Clin Med. 2024 Aug 23;13(17):4995. doi: 10.3390/jcm13174995.
5
Clinical relevance of double heterozygosity revealed by next-generation sequencing of homologous recombination repair pathway genes in South African breast cancer patients.下一代测序揭示南非乳腺癌患者同源重组修复途径基因的双重杂合性的临床意义。
Breast Cancer Res Treat. 2024 Sep;207(2):331-342. doi: 10.1007/s10549-024-07362-2. Epub 2024 May 30.
6
High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders.通过对 DNA 修复障碍的多组学研究进行高可信度的癌症患者分层。
Cell Death Dis. 2022 Nov 26;13(11):999. doi: 10.1038/s41419-022-05437-w.
7
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Radiat Oncol. 2022 Oct 5;17(1):163. doi: 10.1186/s13014-022-02131-1.
8
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9
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10
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J Clin Res Pediatr Endocrinol. 2022 Jun 7;14(2):251-257. doi: 10.4274/jcrpe.galenos.2021.2021.0151. Epub 2021 Sep 21.
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4
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5
Pathology of hereditary breast cancer.遗传性乳腺癌的病理学。
Cell Oncol (Dordr). 2011 Apr;34(2):71-88. doi: 10.1007/s13402-011-0010-3. Epub 2011 Feb 19.
6
Breast cancer in 2010: Novel targets and therapies for a personalized approach.2010 年的乳腺癌:针对个体化方法的新靶点和新疗法。
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7
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9
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Clin Cancer Res. 2008 Jul 1;14(13):4053-8. doi: 10.1158/1078-0432.CCR-08-0098.
10
Synthesis of genetic association studies for pertinent gene-disease associations requires appropriate methodological and statistical approaches.对相关基因与疾病关联进行基因关联研究的综合分析需要适当的方法学和统计学方法。
J Clin Epidemiol. 2008 Jul;61(7):634-45. doi: 10.1016/j.jclinepi.2007.12.011.