糖尿病肾病基因调控网络构建及关键基因识别

R. Zheng, Yun Wang, Zhaoying Lyu, A. Armaou
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引用次数: 1

摘要

糖尿病肾病(DN)是严重危害人类健康的糖尿病并发症。其发病机制涉及多种因素。本文的目的是确定疾病进展中的关键基因,这些基因将成为DN的潜在治疗靶点。根据基因表达谱和蛋白-蛋白、转录因子-基因、转录因子- mirnas和mirnas -基因相互作用数据库,筛选DN差异表达基因。建立了DN差异基因调控网络,利用实体语法系统对DN关键基因进行了识别。根据基因间的调控相互作用,将关键基因定义为能够调控其他基因从异常状态向正常表达的基因。确定的关键基因包括BMP2(骨形态发生蛋白2)、VEGFA(血管内皮生长因子A)、F3(凝血因子III/组织因子)、EGR2(早期生长反应蛋白2)、CDS1 (CDP-二酰基甘油合成酶1)和PLCE1(磷脂酶C epsilon 1)。这些发现为DN药物的成功开发提供了线索。
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Gene Regulatory Network Construction and Key Gene Recognition of Diabetic Nephropathy
Diabetic nephropathy (DN) is a diabetic complication that seriously endangers human health. Its pathogenesis involves a variety of factors. The purpose of this paper is to determine key genes in the disease progression that will be potential therapeutic targets of DN. Based on gene expression profiles and the databases of interactions of proteins-proteins, transcription factors-genes, transcription factors-miRNAs and miRNAs-genes, the differentially expressed genes of DN were screened. The regulatory network of DN differential genes was established and key genes of DN were identified using the entity grammar system. According to the regulatory interaction between genes, key genes were defined as the ones that could regulate the state of other genes from abnormal towards normal expression. Identified key genes include BMP2 (bone morphogenetic protein 2), VEGFA (vascular endothelial growth factor A), F3 (coagulation factor III/tissue factor), EGR2 (early growth response protein 2), CDS1 (CDP- diacylglycerol synthase 1) and PLCE1 (phospholipase C epsilon 1). These findings provide clues for the successful drug development of DN.
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