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癫痫相关神经节细胞胶质瘤中LRP12 C-rs9694676等位基因启动子变体的丰度。

Abundance of LRP12 C-rs9694676 allelic promoter variant in epilepsy-associated gangliogliomas.

作者信息

Robens Barbara K, Gembé Eva, Fassunke Jana, Becker Albert J, Schoch Susanne, Grote Alexander

机构信息

Dept. of Neuropathology/Section for Translational Epilepsy Research, Germany.

Dept. of Pathology, University Clinic of Cologne, Germany.

出版信息

Life Sci. 2016 Jun 15;155:70-5. doi: 10.1016/j.lfs.2016.01.049. Epub 2016 Apr 30.

Abstract

AIMS

Chronic epilepsy associated gangliogliomas (GGs) represent tumors composed of irregularly distributed, often dysmorphic, neurons and neoplastic astroglia. The pathogenesis of GGs is largely unknown. Low-density lipoprotein receptor-related protein 12 (LRP12) is critical for brain development and involved in tumorigenesis of non-cerebral neoplasms.

MAIN METHODS

Here, we have examined a potential role of LRP12 in the pathogenesis of GGs by a combination of mRNA quantification and molecular-biological in vitro assays.

KEY FINDINGS

We observed a significant increase of the single nucleotide polymorphism (SNP) rs9694676 C-allele, located in the LRP12 promoter, in GGs compared to normal control individuals. C-allele expression is correlated with abundant seizure frequency. Expression of LRP12 was lower in GGs than in control brain. In luciferase assays, the C-allele of rs9694676 decreases both, the basal LRP12 core promoter activity and the stimulatory effect of the transcription factor (TF) STAT5a.

SIGNIFICANCE

Accumulation of functional promoter-associated allelic variants with impact on the transcriptional regulation of LRP12 provides a new pathomechanism for GGs, i.e. highly differentiated epileptogenic brain tumors.

摘要

目的

慢性癫痫相关神经节胶质瘤(GGs)是由分布不规则、常呈发育异常的神经元和肿瘤性星形胶质细胞组成的肿瘤。GGs的发病机制在很大程度上尚不清楚。低密度脂蛋白受体相关蛋白12(LRP12)对脑发育至关重要,并参与非脑肿瘤的肿瘤发生过程。

主要方法

在此,我们通过mRNA定量和分子生物学体外试验相结合的方法,研究了LRP12在GGs发病机制中的潜在作用。

关键发现

我们观察到,与正常对照个体相比,位于LRP12启动子区的单核苷酸多态性(SNP)rs9694676的C等位基因在GGs中显著增加。C等位基因表达与癫痫发作频率高相关。GGs中LRP12的表达低于对照脑。在荧光素酶试验中,rs9694676的C等位基因降低了基础LRP12核心启动子活性以及转录因子(TF)STAT5a的刺激作用。

意义

功能性启动子相关等位基因变异的积累对LRP12转录调控产生影响,为GGs(即高度分化的致痫性脑肿瘤)提供了一种新的发病机制。

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