转录组
医学
颌下腺
病理
计算生物学
疾病
基因表达
基因
遗传学
生物
作者
Motohisa Yamamoto,Ryuta Kamekura,Masaaki Uehara,Yuta Ichii,T Tanaka,Satsuki Aochi,Kenichi Takano
出处
期刊:Rheumatology
[Oxford University Press]
日期:2024-07-26
被引量:2
标识
DOI:10.1093/rheumatology/keae393
摘要
Abstract Objective To identify genes that could provide clues leading to the discovery of drugs to treat IgG4-related disease (IgG4-RD). Methods Submandibular gland tissue bulk RNAseq analysis of 45 cases with a definite diagnosis of IgG4-RD was integrated with Visium spatial transcriptome analysis of two cases to identify pathogenic genes expressed in tertiary lymphoid tissues. Results Bulk RNAseq and pathway analyses showed upregulation of cell cycle and T cell-related signals in IgG4-RD. Spatial transcriptome analysis identified the cluster corresponding to germinal centres and the top 38 common genes that showed significant variations in expression compared with other clusters. The top 20 genes were extracted by comparing the bulk RNAseq data. Network analysis identified CDK1 as the gene most strongly associated of the top 20 genes. Conclusion The CDK1 gene may be a regulator of the pathogenesis of IgG4-RD and provide clues for drug discovery.
科研通智能强力驱动
Strongly Powered by AbleSci AI