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与格雷夫斯病发病机制相关的关键基因共表达模块和功能途径。

Key gene co-expression modules and functional pathways involved in the pathogenesis of Graves' disease.

机构信息

Department of Endocrinology, Jinshan Hospital of Fudan University, Shanghai 201508, China.

Department of Endocrinology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, Shanghai 201318, China.

出版信息

Mol Cell Endocrinol. 2018 Oct 15;474:252-259. doi: 10.1016/j.mce.2018.03.015. Epub 2018 Mar 31.

Abstract

Graves' disease (GD) is a common autoimmune thyroid disease characterized by positive thyroid stimulating hormone receptor antibody. To better understand its molecular pathogenesis, we adopted the weighted gene co-expression network analysis to reveal co-expression modules of key genes involved in the pathogenesis of GD, protein-protein interaction network analysis to identify the hub genes related to GD development and functional analyses to explore their possible functions. Our results showed that 1) a total of 2667 differentially expressed genes in our microarray study and 16 different gene co-expression modules were associated with GD, and 2) the most significant module was associated with the percentage of macrophages, T follicular helper cells and CD4 memory T cells and mainly enriched in immune regulation and immune response. Overall, our study reveals several key gene co-expression modules and functional pathways involved in GD, which provides some novel insights into the pathogenesis of GD.

摘要

格雷夫斯病(GD)是一种常见的自身免疫性甲状腺疾病,其特征是促甲状腺激素受体抗体阳性。为了更好地了解其分子发病机制,我们采用加权基因共表达网络分析来揭示与 GD 发病机制相关的关键基因的共表达模块、蛋白质-蛋白质相互作用网络分析来鉴定与 GD 发展相关的枢纽基因,并进行功能分析以探讨其可能的功能。我们的研究结果表明:1)我们的基因芯片研究中共有 2667 个差异表达基因和 16 个不同的基因共表达模块与 GD 相关,2)最显著的模块与巨噬细胞、滤泡辅助 T 细胞和 CD4 记忆 T 细胞的百分比相关,主要富集在免疫调节和免疫反应中。总的来说,我们的研究揭示了 GD 涉及的几个关键基因共表达模块和功能途径,为 GD 的发病机制提供了一些新的见解。

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