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9q22.33、14q13.3和ATM基因座的常见变异与古巴人群分化型甲状腺癌风险

Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population.

作者信息

Pereda Celia M, Lesueur Fabienne, Pertesi Maroulio, Robinot Nivonirina, Lence-Anta Juan J, Turcios Silvia, Velasco Milagros, Chappe Mae, Infante Idalmis, Bustillo Marlene, García Anabel, Clero Enora, Xhaard Constance, Ren Yan, Maillard Stéphane, Damiola Francesca, Rubino Carole, Salazar Sirced, Rodriguez Regla, Ortiz Rosa M, de Vathaire Florent

机构信息

Institute of Oncology and Radiobiology, Havana, Cuba.

The French National Institute of Health and Medical Research (Inserm), U900, Institut Curie, Mines ParisTech, Paris, F-75005, France.

出版信息

BMC Genet. 2015 Mar 1;16:22. doi: 10.1186/s12863-015-0180-5.

Abstract

BACKGROUND

The incidence of differentiated thyroid carcinoma (DTC) in Cuba is low and the contribution of host genetic factors to DTC in this population has not been investigated so far. Our goal was to assess the role of known risk polymorphisms in DTC cases living in Havana. We genotyped five polymorphisms located at the DTC susceptibility loci on chromosome 14q13.3 near NK2 homeobox 1 (NKX2-1), on chromosome 9q22.33 near Forkhead factor E1 (FOXE1) and within the DNA repair gene Ataxia-Telangiectasia Mutated (ATM) in 203 cases and 212 age- and sex- matched controls. Potential interactions between these polymorphisms and other DTC risk factors such as body surface area, body mass index, size, ethnicity, and, for women, the parity were also examined.

RESULTS

Significant association with DTC risk was found for rs944289 near NKX2-1 (OR per A allele = 1.6, 95% CI: 1.2-2.1), and three polymorphisms near or within FOXE1, namely rs965513 (OR per A allele = 1.7, 95% CI: 1.2-2.3), rs1867277 in the promoter region of the gene (OR per A allele = 1.5, 95% CI: 1.1-1.9) and the poly-alanine tract expansion polymorphism rs71369530 (OR per Long Allele = 1.8, 95% CI: 1.3-2.5), only the 2 latter remaining significant when correcting for multiple tests. Overall, no association between DTC and the coding SNP D1853N (rs1801516) in ATM (OR per A Allele = 1.1, 95% CI: 0.7-1.7) was seen. Nevertheless women who had 2 or more pregnancies had a 3.5-fold increase in risk of DTC if they carried the A allele (OR 3.5, 95% CI: 3.2-9.8) as compared to 0.8 (OR 0.8, 95% CI: 0.4-1.6) in those who had fewer than 2.

CONCLUSIONS

We confirmed in the Cuban population the role of the loci previously associated with DTC susceptibility in European and Japanese populations through genome-wide association studies. Our results on ATM and the number of pregnancies raise interesting questions on the mechanisms by which oestrogens, or other hormones, alter the DNA damage response and DNA repair through the regulation of key effector proteins such as ATM. Due to the small size of our study and to multiple tests, all these results warrant further investigation.

摘要

背景

古巴分化型甲状腺癌(DTC)的发病率较低,目前尚未对该人群中宿主遗传因素对DTC的影响进行研究。我们的目标是评估已知风险多态性在居住于哈瓦那的DTC患者中的作用。我们对203例患者和212例年龄及性别匹配的对照者进行了基因分型,这五个多态性分别位于14号染色体q13.3上靠近NK2同源盒1(NKX2-1)的DTC易感位点、9号染色体q22.33上靠近叉头因子E1(FOXE1)的位置以及DNA修复基因共济失调毛细血管扩张症突变基因(ATM)内。我们还研究了这些多态性与其他DTC风险因素之间的潜在相互作用,如体表面积、体重指数、肿瘤大小、种族,以及女性的生育次数。

结果

发现靠近NKX2-1的rs944289与DTC风险显著相关(每个A等位基因的OR = 1.6,95% CI:1.2 - 2.1),以及FOXE1附近或内部的三个多态性,即rs965513(每个A等位基因的OR = 1.7,95% CI:1.2 - 2.3)、该基因启动子区域的rs1867277(每个A等位基因的OR = 1.5,95% CI:1.1 - 1.9)和多聚丙氨酸重复序列扩展多态性rs71369530(每个长等位基因的OR = 1.8,95% CI:1.3 - 2.5),仅后两者在进行多重检验校正后仍具有显著性。总体而言,未发现DTC与ATM中的编码SNP D1853N(rs1801516)之间存在关联(每个A等位基因的OR = 1.1,95% CI:0.7 - 1.7)。然而,生育2次或更多次的女性若携带A等位基因,其患DTC的风险增加3.5倍(OR 3.5,95% CI:3.2 - 9.8),而生育次数少于2次的女性该风险为0.8(OR 0.8,95% CI:0.4 - 1.6)。

结论

我们在古巴人群中证实了先前通过全基因组关联研究在欧洲和日本人群中发现的与DTC易感性相关的位点的作用。我们关于ATM和生育次数的研究结果提出了有趣的问题,即雌激素或其他激素通过调节关键效应蛋白如ATM来改变DNA损伤反应和DNA修复的机制。由于我们的研究规模较小且进行了多次检验,所有这些结果都需要进一步研究。

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