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The Differential Expression of Circular RNAs in Type 2 Diabetes Mellitus and Latent Autoimmune Diabetes in Adults

机译:圆形rna的微分表达式2型糖尿病和潜在的自身免疫性成人糖尿病

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Objective: Expression of circular RNAs (circRNAs) in the peripheral blood of individuals with latent autoimmune diabetes in adults (LADA) and type 2 diabetes mellitus (T2DM) were quantified to identify dysregulated circRNAs compared with control individuals.Methods: circRNAs were obtained from the peripheral blood serum of 12 healthy adults and 12 individuals with LADA and 12 type 2 diabetics. The circRNA expression profiles were analyzed by high-throughput RNA sequencing. The most highly dysregulated circular RNAs were validated by quantitative real-time polymerase chain reaction. A circular RNA-microRNA (miRNA) network diagram predicted the interactions of circular RNAs, miRNAs, and coding genes.Results: A total of 2334 differentially expressed circRNAs were detected among the three groups, with 277 circRNAs in the Group DM versus Group NG; 992 circRNAs in the Group LADA versus Group NG and 1065 circRNAs in the Group DM versus Group LADA. Six circRNAs were identified as the most distinctive differentially expressed targets (p < 0.05). The proposed molecular functions of these differentially expressed circRNAS included the tumor necrosis factor signaling pathway, the FoxO signaling pathway, cellular senescence, and long-term potentiation (all false discovery rate p < 0.05) which may contribute to T2DM and LADA.Conclusion: circRNAs are aberrantly expressed in the peripheral blood of patients with T2DM and LADA and may interact with miRNA and circRNA-derived peptides in the development of diabetes. Further investigations may illustrate the partial pathogenesis of diabetes mellitus.Clinical Trial Registration number: ChiCTR1900020644.
机译:摘要目的:圆形rna的表达(circRNAs)在患者的外周血潜在的自身免疫性糖尿病成年人(拉达)2型糖尿病(T2DM)病人体内被量化识别circRNAs而特异表达控制个人。获得的外周血血清12健康成人和12个人和拉达12 2型糖尿病。概要分析了高通量RNA测序。rna被定量实时验证聚合酶链反应。预测RNA-microRNA (microrna)网络图循环rna的交互,microrna编码基因。差异表达circRNAs被检测到在三组中,277 circRNAsNG组DM与组;NG组拉达和组和1065年circRNAsDM组与组拉达。确认为最独特的差异表示目标(p < 0.05)。这些不同的分子功能表示circRNAS包括肿瘤坏死FoxO信号因子信号通路通路、细胞衰老和长期的增强作用(所有的错误发现率p < 0.05)这可能导致2型糖尿病和拉达。circRNAs中异常表达二型糖尿病患者的外周血和拉达可能与microrna的交互和circRNA-derived肽在糖尿病的发展。调查可能说明部分糖尿病的发病机制。注册号:ChiCTR1900020644。

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