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通过转录组分析研究结节性硬化症伴癫痫患者的围小管组织的重要作用。

The Important Role of Perituberal Tissue in Epileptic Patients with Tuberous Sclerosis Complex by the Transcriptome Analysis.

机构信息

Department of Urology, The First Affiliated Hospital of Zhengzhou University, No. 1 Jianshe East Road, Zhengzhou, Henan 450052, China.

Department of Neuro Intensive Care Unit, The First Affiliated Hospital of Zhengzhou University, No. 1 Jianshe East Road, Zhengzhou, Henan 450052, China.

出版信息

Biomed Res Int. 2020 Oct 15;2020:4980609. doi: 10.1155/2020/4980609. eCollection 2020.

Abstract

Epilepsy is most common in patients with tuberous sclerosis complex (TSC). However, in addition to the challenging treatment, the pathogenesis of epilepsy is still controversial. To determine the transcriptome characteristics of perituberal tissue (PT) and clarify its role in the pathogenesis of epilepsy, GSE16969 was downloaded from the GEO database for further study by comprehensive bioinformatics analysis. Identification of differentially expressed genes (DEGs), functional enrichment analysis, construction of protein-protein interaction (PPI) network, and selection of Hub genes were performed using R language, Metascape, STRING, and Cytoscape, respectively. Comparing with cortical tuber (CT), 220 DEGs, including 95 upregulated and 125 downregulated genes, were identified in PT and mainly enriched in collagen-containing extracellular matrix and positive regulation of receptor-mediated endocytosis, as well as the pathways of ECM-receptor interaction and neuroactive ligand-receptor interaction. As for normal cortex (NC), 1549 DEGs, including 30 upregulated and 1519 downregulated genes, were identified and mainly enriched in presynapse, dendrite and axon, and also the pathways of dopaminergic synapse and oxytocin signaling pathway. In the PPI network, 4 hub modules were found between PT and CT, and top 5 hub modules were selected between PT and NC. C3, APLNR, ANXA2, CD44, CLU, CP, MCHR2, HTR1E, CTSG, APP, and GNG2 were identified as Hub genes, of which, C3, CD44, ANXA2, HTR1E, and APP were identified as Hub-BottleNeck genes. In conclusion, PT has the unique characteristics different from CT and NC in transcriptome and makes us further understand its importance in the TSC-associated epilepsy.

摘要

癫痫最常见于结节性硬化症复合征(TSC)患者。然而,除了具有挑战性的治疗外,癫痫的发病机制仍存在争议。为了确定结节旁组织(PT)的转录组特征,并阐明其在癫痫发病机制中的作用,从 GEO 数据库下载 GSE16969 并通过综合生物信息学分析进一步研究。使用 R 语言、Metascape、STRING 和 Cytoscape 分别进行差异表达基因(DEGs)鉴定、功能富集分析、蛋白质-蛋白质相互作用(PPI)网络构建和 Hub 基因选择。与皮质结节(CT)相比,PT 中鉴定出 220 个 DEGs,包括 95 个上调基因和 125 个下调基因,主要富集在含有胶原蛋白的细胞外基质和受体介导的内吞的正调节,以及细胞外基质-受体相互作用和神经活性配体-受体相互作用途径。与正常皮质(NC)相比,在 NC 中鉴定出 1549 个 DEGs,包括 30 个上调基因和 1519 个下调基因,主要富集在突触前、树突和轴突,以及多巴胺能突触和催产素信号通路。在 PPI 网络中,在 PT 和 CT 之间发现了 4 个枢纽模块,在 PT 和 NC 之间选择了前 5 个枢纽模块。C3、APLNR、ANXA2、CD44、CLU、CP、MCHR2、HTR1E、CTSG、APP 和 GNG2 被鉴定为枢纽基因,其中 C3、CD44、ANXA2、HTR1E 和 APP 被鉴定为枢纽瓶颈基因。总之,PT 在转录组上具有与 CT 和 NC 不同的独特特征,使我们进一步了解其在 TSC 相关癫痫中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78cc/7585662/c93cac06534c/BMRI2020-4980609.001.jpg

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