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MAP3K10 基因的 DNA 甲基化可能参与颅内动脉瘤的发生。

DNA methylation of the MAP3K10 gene may participate in the development of intracranial aneurysm.

机构信息

Department of Neurosurgery, Ningbo First Hospital, Ningbo Hospital of Zhejiang University, Ningbo, Zhejiang 315010, China.

Department of Neurology, Ningbo First Hospital, Ningbo Hospital of Zhejiang University, Ningbo, Zhejiang 315010, China.

出版信息

Gene. 2023 Jan 30;851:147024. doi: 10.1016/j.gene.2022.147024. Epub 2022 Oct 29.

Abstract

BACKGROUND

The goal of this study was to explore the association between mitogen-activated protein kinase kinase kinase 10 (MAP3K10) methylation and blood lipid levels and intracranial aneurysm (IA) risk.

MATERIALS AND METHODS

A total of 96 age- and sex-matched investigators participated in the assessment of MAP3K10 methylation. Fourteen CpG sites of the MAP3K10 gene were selected for methylated-pyrosequencing. Human brain vascular smooth muscle cell was used to assess the regulatory role of DNA methylation in MAP3K10 gene transcription.

RESULTS

MAP3K10 mean methylation was positively correlated with triglyceride (TG, r = 0.388; p = 0.007) in men, but negatively correlated with TG (r = -0.434; p = 0.002) in women. MAP3K10 methylation in patients with IA was significantly lower than that in controls (p < 0.05), and this phenomenon was more significant in women (12 CpG sites presented significance at p < 0.05). MAP3K10 methylation might be a potential predictor of the risk of IA (CpG1, AUC = 0.81, p < 0.001; mean methylation, AUC = 0.69, p = 0.001). The predictive value was also more significant in women (CpG1: AUC = 0.86, p < 0.001; mean methylation: AUC = 0.73, p = 0.006). No significant association was found between DNA methylation and MAP3K10 gene transcription in vitro experiment.

CONCLUSION

Patients with IA had lower MAP3K10 methylation levels than healthy controls. MAP3K10 methylation may be a potential predictor of IA risk, particularly in women.

摘要

背景

本研究旨在探讨丝裂原活化蛋白激酶激酶激酶 10(MAP3K10)甲基化与血脂水平和颅内动脉瘤(IA)风险之间的关系。

材料与方法

共有 96 名年龄和性别匹配的研究人员参与了 MAP3K10 甲基化评估。选择 MAP3K10 基因的 14 个 CpG 位点进行甲基化焦磷酸测序。用人脑血管平滑肌细胞评估 DNA 甲基化对 MAP3K10 基因转录的调节作用。

结果

男性中 MAP3K10 平均甲基化与甘油三酯(TG)呈正相关(r=0.388;p=0.007),而女性中 MAP3K10 平均甲基化与 TG 呈负相关(r=-0.434;p=0.002)。IA 患者的 MAP3K10 甲基化水平明显低于对照组(p<0.05),且这种现象在女性中更为显著(12 个 CpG 位点在 p<0.05 时有显著性)。MAP3K10 甲基化可能是 IA 风险的潜在预测指标(CpG1,AUC=0.81,p<0.001;平均甲基化,AUC=0.69,p=0.001)。在女性中,该预测价值更为显著(CpG1:AUC=0.86,p<0.001;平均甲基化:AUC=0.73,p=0.006)。体外实验中未发现 DNA 甲基化与 MAP3K10 基因转录之间存在显著相关性。

结论

IA 患者的 MAP3K10 甲基化水平低于健康对照组。MAP3K10 甲基化可能是 IA 风险的潜在预测指标,尤其是在女性中。

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