Up-Regulation of S100 Gene Family in Brain Samples of a Subgroup of Individuals with Schizophrenia: Meta-analysis.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-09-01 Epub Date: 2023-04-02 DOI:10.1007/s12017-023-08743-4
Anat Shamir, Assif Yitzhaky, Aviv Segev, Vahram Haroutunian, Pavel Katsel, Libi Hertzberg
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引用次数: 1

Abstract

The S100 proteins family is known to affect neuroinflammation and astrocyte activation, which have been suggested to be contributors to the pathogenesis of schizophrenia. We conducted a systematic meta-analysis of S100 genes differential expression in postmortem samples of patients with schizophrenia vs. healthy controls, following the commonly used Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. Twelve microarray datasets met the inclusion criteria (overall 511 samples, 253 schizophrenia and 258 controls were analyzed). Nine out of 21 genes were significantly up-regulated or with tendency for up-regulation. A per-sample fold change analysis indicated that the S100 genes' up-regulation was concentrated in a subgroup of the patients. None of the genes have been found to be down-regulated. ANXA3, which encodes Annexin 3 protein and was associated with neuroinflammation, was up-regulated and positively correlated with the S100 genes' expression pattern. In addition, astrocytes and endothelial cell markers were significantly correlated with S100A8 expression. S100 correlation with ANXA3 and endothelial cell markers suggests that the up-regulation we detected reflects increased inflammation. However, it might also reflect astrocytes abundance or activation. The fact that S100 proteins were shown to be up-regulated in blood samples and other body fluids of patients with schizophrenia suggests a potential role as biomarkers, which might help disease subtyping, and the development of etiological treatments for immune dysregulation in schizophrenia.

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精神分裂症患者脑样本中S100基因家族的上调:荟萃分析。
众所周知,S100蛋白家族会影响神经炎症和星形胶质细胞的激活,这被认为是精神分裂症发病机制的因素。我们根据常用的系统评价和荟萃分析首选报告项目(PRISMA)指南,对精神分裂症患者与健康对照组死后样本中S100基因的差异表达进行了系统荟萃分析。12个微阵列数据集符合纳入标准(共分析了511个样本、253个精神分裂症患者和258个对照组)。21个基因中有9个显著上调或有上调趋势。每个样本的倍数变化分析表明,S100基因的上调集中在患者的一个亚组中。没有发现任何基因被下调。ANXA3编码膜联蛋白3蛋白,与神经炎症相关,上调并与S100基因的表达模式呈正相关。此外,星形胶质细胞和内皮细胞标志物与S100A8的表达显著相关。S100与ANXA3和内皮细胞标志物的相关性表明,我们检测到的上调反映了炎症的增加。然而,它也可能反映星形胶质细胞的丰度或活化。事实上,S100蛋白在精神分裂症患者的血液样本和其他体液中被证明是上调的,这表明其作为生物标志物的潜在作用,可能有助于疾病的分型,并开发精神分裂症免疫失调的病因治疗方法。
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CiteScore
7.20
自引率
4.30%
发文量
567
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