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