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基因多态性与中国儿童神经母细胞瘤易感性。

gene polymorphisms and neuroblastoma susceptibility in Chinese children.

机构信息

Department of Pediatric Surgery, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan 250012, Shandong, China.

Department of Pediatric Surgery, Hunan Children's Hospital, Changsha 410004, Hunan, China.

出版信息

Aging (Albany NY). 2021 Dec 12;13(23):25426-25439. doi: 10.18632/aging.203760.

Abstract

Neuroblastoma (NB) is the most common extracranial tumor in children. YTHDC1, a member of RNA methylation modification binding proteins, plays critical roles in tumor occurrence and metastasis. However, it is unclear whether gene polymorphisms are related to NB susceptibility. Herein, we aimed to evaluate the association between gene polymorphisms (rs2293596 T>C, rs2293595 T>C, rs3813832 T>C) and susceptibility of NB by logistic regression models. In this eight-center case-control study, 898 patients with NB and 1734 healthy controls were genotyped by TaqMan assay. The results showed that rs3813832 TC genotype could significantly reduce the susceptibility of NB compared with the TT genotype [adjusted odds ratio (AOR) = 0.81, 95% confidence interval (CI) = 0.68-0.96, = 0.018]. Combined genotype analysis revealed that individuals with 3 protective genotypes had a prominently lower NB risk than those with 0-2 protective genotypes (AOR = 0.80, 95% CI = 0.68-0.94, = 0.006). The stratified analysis also demonstrated the protective effect of rs3813832 TC/CC and 3 protective genotypes in certain subgroups. Further functional experiments revealed that siRNA-554, targeting the area near the rs3813832 T>C polymorphism site, could observably inhibit the proliferation and migration of NB cells. In conclusion, our findings highlight the involvement of gene and its genetic variants in the etiology of NB.

摘要

神经母细胞瘤(NB)是儿童最常见的颅外肿瘤。YTHDC1 是 RNA 甲基化修饰结合蛋白的成员,在肿瘤发生和转移中发挥着关键作用。然而,目前尚不清楚基因多态性是否与 NB 的易感性有关。在此,我们旨在通过逻辑回归模型评估基因多态性(rs2293596 T>C、rs2293595 T>C、rs3813832 T>C)与 NB 易感性之间的关联。在这项八中心病例对照研究中,898 例 NB 患者和 1734 例健康对照者通过 TaqMan 检测进行了基因分型。结果显示,与 TT 基因型相比,rs3813832 TC 基因型可显著降低 NB 的易感性[校正比值比(AOR)=0.81,95%置信区间(CI)=0.68-0.96,=0.018]。联合基因型分析表明,与 0-2 个保护性基因型相比,具有 3 个保护性基因型的个体患 NB 的风险显著降低(AOR=0.80,95%CI=0.68-0.94,=0.006)。分层分析还表明,rs3813832 TC/CC 及 3 个保护性基因型在某些亚组中具有保护作用。进一步的功能实验表明,靶向 rs3813832 T>C 多态性位点附近区域的 siRNA-554 可明显抑制 NB 细胞的增殖和迁移。综上所述,本研究结果提示基因及其遗传变异可能参与 NB 的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a706/8714171/7c7cdabf8422/aging-13-203760-g001.jpg

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