脱甲基酶
FTO基因
调解人
临床意义
医学
背景(考古学)
计算生物学
癌症
生物信息学
基因表达
药物发现
药理学
神经科学
N6-甲基腺苷
人体研究
小RNA
小分子
对接(动物)
核糖核酸
基因表达调控
细胞色素P450
仿形(计算机编程)
生物
基因
表观遗传学
作者
Cun-Yang Guo,Yifei Du,Hui-cong Yan,Xin-ming Fan,Fang-Qi Tian,Ping Xu
标识
DOI:10.14336/ad.2025.0916
摘要
A), thereby influencing RNA splicing, stability, and translation. This regulatory activity plays a major role in processes such as inflammation and fibrosis. Dysregulation of FTO has been implicated in several non-malignant diseases, including metabolic disorders, neurological diseases, and cardiovascular conditions. Computational docking studies showed that FTO exhibited strong binding affinity with two drugs and moderate affinity with eight others. Bibliometric analysis revealed high-frequency keywords and visualized research hotspots pertaining to FTO, providing valuable insight into current areas of scientific interest and potential future directions of study. FTO functions as a key epigenetic regulator in non-cancerous diseases and represents a promising biomarker and therapeutic target. Our findings underscore the importance of FTO-drug interactions and suggest that small-molecule FTO modulators may hold therapeutic value for managing a variety of non-oncologic conditions.
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