溃疡性结肠炎
鉴定(生物学)
基因
计算生物学
生物
遗传学
医学
植物
病理
疾病
作者
Xinyu Bai,Fengrui Zhang,Chan Zhou,Jingxian Yan,Hao Liang,Rui Zhu,Min Gong,Huixian Song,Junkun Niu,Yinglei Miao
出处
期刊:Heliyon
[Elsevier BV]
日期:2024-01-01
卷期号:10 (2): e24875-e24875
被引量:4
标识
DOI:10.1016/j.heliyon.2024.e24875
摘要
Ulcerative colitis (UC) is a refractory inflammatory disease with imbalances in intestinal mucosal homeostasis. Cuproptosis serves as newly identified programmed cell death (PCD) form involved in UC. In the study, UC-related datasets were extracted from the Gene Expression Omnibus (GEO) database. A comparison of UC patients and healthy controls identified 11 differentially expressed cuproptosis-related genes (DE-CRGs), where FDX1, LIAS, and DLAT were differentially expressed in UC groups from the mouse models and clinical samples, with their expression correlating with disease severity. By comprehending weighted gene co-expression network analysis (WGCNA) and differential expression analysis, the key genes common to the module genes relevant to different cuproptosis-related clusters and differentially expressed genes (DEGs) both in different clusters and patients with and without UC were identified using several bioinformatic analysis. Furthermore, the mRNA levels of four characteristic genes with diagnostic potential demonstrated significant decrease in both mouse models and clinical UC samples. Our discoveries offer a theoretical foundation for cuproptosis effect in UC.
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