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rs10454142与乳腺癌的肥胖相关关联。

Obesity-Dependent Association of the rs10454142 with Breast Cancer.

作者信息

Ponomarenko Irina, Pasenov Konstantin, Churnosova Maria, Sorokina Inna, Aristova Inna, Churnosov Vladimir, Ponomarenko Marina, Reshetnikova Yuliya, Reshetnikov Evgeny, Churnosov Mikhail

机构信息

Department of Medical Biological Disciplines, Belgorod State National Research University, 308015 Belgorod, Russia.

出版信息

Biomedicines. 2024 Apr 8;12(4):818. doi: 10.3390/biomedicines12040818.

Abstract

The purpose of this work was to find a link between the breast cancer (BC)-risk effects of sex hormone-binding globulin (SHBG)-associated polymorphisms and obesity. The study was conducted on a sample of 1498 women (358 BC; 1140 controls) who, depending on the presence/absence of obesity, were divided into two groups: obese (119 BC; 253 controls) and non-obese (239 BC; 887 controls). Genotyping of nine SHBG-associated single nucleotide polymorphisms (SNP)-rs17496332 , rs780093 , rs10454142 , rs3779195 , rs440837 , rs7910927 , rs4149056 , rs8023580 , and rs12150660 -was executed, and the BC-risk impact of these loci was analyzed by logistic regression separately in each group of obese/non-obese women. We found that the BC-risk effect correlated by GWAS with the SHBG-level polymorphism rs10454142 depends on the presence/absence of obesity. The SHBG-lowering allele C rs10454142 has a risk value for BC in obese women (allelic model: CT, OR = 1.52, 95%CI = 1.10-2.11, and p = 0.013; additive model: CCTCTT, OR = 1.71, 95%CI = 1.15-2.62, and p = 0.011; dominant model: CC + TCTT, OR = 1.95, 95%CI = 1.13-3.37, and p = 0.017) and is not associated with the disease in women without obesity. SNP rs10454142 and 10 proxy SNPs have adipose-specific regulatory effects (epigenetic modifications of promoters/enhancers, DNA interaction with 51 transcription factors, eQTL/sQTL effects on five genes (, , , , and ), etc.), can be "likely cancer driver" SNPs, and are involved in cancer-significant pathways. In conclusion, our study detected an obesity-dependent association of the rs10454142 with BC in women.

摘要

这项研究的目的是找出性激素结合球蛋白(SHBG)相关多态性的乳腺癌(BC)风险效应与肥胖之间的联系。该研究对1498名女性样本(358例乳腺癌患者;1140例对照)进行,这些女性根据是否肥胖被分为两组:肥胖组(119例乳腺癌患者;253例对照)和非肥胖组(239例乳腺癌患者;887例对照)。对9个与SHBG相关的单核苷酸多态性(SNP)——rs17496332、rs780093、rs10454142、rs3779195、rs440837、rs7910927、rs4149056、rs8023580和rs12150660进行基因分型,并分别在肥胖/非肥胖女性的每组中通过逻辑回归分析这些位点对BC风险的影响。我们发现,通过全基因组关联研究(GWAS)与SHBG水平多态性rs10454142相关的BC风险效应取决于是否存在肥胖。降低SHBG的rs10454142等位基因C在肥胖女性中具有BC风险值(等位基因模型:CT,比值比(OR)=1.52,95%置信区间(CI)=1.10 - 2.11,p = 0.013;加性模型:CCTCTT,OR = 1.71,95%CI = 1.15 - 2.62,p = 0.011;显性模型:CC + TCTT,OR = 1.95,95%CI = 1.13 - 3.37,p = 0.017),而在非肥胖女性中与该疾病无关。SNP rs10454142和10个代理SNP具有脂肪特异性调节作用(启动子/增强子的表观遗传修饰、DNA与51种转录因子的相互作用、对五个基因(、、、、和)的表达数量性状位点/剪接数量性状位点效应等),可能是“潜在的癌症驱动”SNP,并参与癌症相关的重要途径。总之,我们的研究检测到女性中rs10454142与BC之间存在肥胖依赖性关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/930e/11048332/da8390c6f05f/biomedicines-12-00818-g001.jpg

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