Suppr超能文献

包括GPR174和GNG2在内的基因表达谱改变与血管迷走性晕厥相关。

Alteration of gene expression profiling including GPR174 and GNG2 is associated with vasovagal syncope.

作者信息

Huang Yu-Juan, Zhou Zai-wei, Xu Miao, Ma Qing-wen, Yan Jing-bin, Wang Jian-yi, Zhang Quo-qin, Huang Min, Bao Liming

机构信息

Shanghai Institute of Medical Genetics, Shanghai Children's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China,

出版信息

Pediatr Cardiol. 2015 Mar;36(3):475-80. doi: 10.1007/s00246-014-1036-x. Epub 2014 Nov 1.

Abstract

Vasovagal syncope (VVS) causes accidental harm for susceptible patients. However, pathophysiology of this disorder remains largely unknown. In an effort to understanding of molecular mechanism for VVS, genome-wide gene expression profiling analyses were performed on VVS patients at syncope state. A total of 66 Type 1 VVS child patients and the same number healthy controls were enrolled in this study. Peripheral blood RNAs were isolated from all subjects, of which 10 RNA samples were randomly selected from each groups for gene expression profile analysis using Gene ST 1.0 arrays (Affymetrix). The results revealed that 103 genes were differently expressed between the patients and controls. Significantly, two G-proteins related genes, GPR174 and GNG2 that have not been related to VVS were among the differently expressed genes. The microarray results were confirmed by qRT-PCR in all the tested individuals. Ingenuity pathway analysis and gene ontology annotation study showed that the differently expressed genes are associated with stress response and apoptosis, suggesting that the alteration of some gene expression including G-proteins related genes is associated with VVS. This study provides new insight into the molecular mechanism of VVS and would be helpful to further identify new molecular biomarkers for the disease.

摘要

血管迷走性晕厥(VVS)会对易感患者造成意外伤害。然而,这种疾病的病理生理学在很大程度上仍不清楚。为了了解VVS的分子机制,对处于晕厥状态的VVS患者进行了全基因组基因表达谱分析。本研究共纳入了66例1型VVS儿童患者和相同数量的健康对照。从所有受试者中分离外周血RNA,每组随机选择10个RNA样本,使用基因ST 1.0芯片(Affymetrix)进行基因表达谱分析。结果显示,患者和对照之间有103个基因表达存在差异。值得注意的是,两个与G蛋白相关且此前与VVS无关的基因GPR174和GNG2也在差异表达基因之中。微阵列结果在所有测试个体中通过qRT-PCR得到了证实。 Ingenuity通路分析和基因本体注释研究表明,差异表达基因与应激反应和细胞凋亡相关,这表明包括与G蛋白相关基因在内的一些基因表达的改变与VVS有关。本研究为VVS的分子机制提供了新的见解,将有助于进一步识别该疾病新的分子生物标志物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验