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2 型糖尿病口渴乏力患者外周血转录组测序分析。

Transcriptome Sequencing Analysis of Peripheral Blood of Type 2 Diabetes Mellitus Patients With Thirst and Fatigue.

机构信息

Traditional Chinese Medicine School, Beijing University of Chinese Medicine, Beijing, China.

Third Affiliated Hospital, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Endocrinol (Lausanne). 2020 Nov 9;11:558344. doi: 10.3389/fendo.2020.558344. eCollection 2020.

Abstract

The purpose of this study is to explore the differences in transcriptome expression profiles between healthy subjects and type 2 diabetes mellitus patients with thirst and fatigue (D-T2DM) and, in addition, to investigate the possible role of noncoding ribonucleic acids (RNAs) in the pathogenesis of D-T2DM. We constructed the expression profiles of RNAs by RNA sequencing in the peripheral blood of D-T2DM patients and healthy subjects and analyzed differentially expressed RNAs. Compared with healthy subjects, a total of 469 mRNAs, 776 long non-coding RNAs (lncRNAs), and 21 circular RNAs (circRNAs) were differentially expressed in D-T2DM patients. Furthermore, several genes associated with insulin resistance, inflammation, and mitochondrial dysfunction were identified within the differentially expressed mRNAs. Differentially expressed lncRNAs were primarily involved in biological processes associated with immune responses. In addition, differentially expressed circRNAs may target miRNAs associated with glucose metabolism and mitochondrial function. Our results may bring a new perspective on differential RNA expression involved in the pathogenesis of D-T2DM and promote the development of novel treatments for this disease.

摘要

本研究旨在探讨健康受试者与伴有口渴和乏力的 2 型糖尿病患者(D-T2DM)之间转录组表达谱的差异,并探讨非编码 RNA(RNAs)在 D-T2DM 发病机制中的可能作用。我们通过对 D-T2DM 患者和健康受试者外周血中的 RNA 进行 RNA 测序,构建了 RNA 的表达谱,并对差异表达的 RNA 进行了分析。与健康受试者相比,D-T2DM 患者中共有 469 个 mRNA、776 个长链非编码 RNA(lncRNAs)和 21 个环状 RNA(circRNAs)差异表达。此外,在差异表达的 mRNAs 中还鉴定出了一些与胰岛素抵抗、炎症和线粒体功能障碍相关的基因。差异表达的 lncRNAs 主要参与与免疫反应相关的生物学过程。此外,差异表达的 circRNAs 可能靶向与葡萄糖代谢和线粒体功能相关的 miRNA。我们的研究结果可能为 D-T2DM 发病机制中涉及的差异 RNA 表达提供新的视角,并促进针对该疾病的新疗法的开发。

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