串扰
癌症研究
肝细胞癌
纤维化
乙酰化
癌变
非酒精性脂肪肝
炎症
生物
泛素
脂肪肝
生物信息学
医学
疾病
免疫学
癌症
内科学
生物化学
物理
光学
基因
作者
Zun Mao,Junpeng Mu,Zhixiang Gao,Shile Huang,Long Chen
出处
期刊:Cells
[MDPI AG]
日期:2024-05-09
卷期号:13 (10): 805-805
标识
DOI:10.3390/cells13100805
摘要
O-linked-β-D-N-acetylglucosamine (O-GlcNAc) glycosylation (O-GlcNAcylation), which is dynamically regulated by O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA), is a post-translational modification involved in multiple cellular processes. O-GlcNAcylation of proteins can regulate their biological functions via crosstalk with other post-translational modifications, such as phosphorylation, ubiquitination, acetylation, and methylation. Liver diseases are a major cause of death worldwide; yet, key pathological features of the disease, such as inflammation, fibrosis, steatosis, and tumorigenesis, are not fully understood. The dysregulation of O-GlcNAcylation has been shown to be involved in some severe hepatic cellular stress, viral hepatitis, liver fibrosis, nonalcoholic fatty acid liver disease (NAFLD), malignant progression, and drug resistance of hepatocellular carcinoma (HCC) through multiple molecular signaling pathways. Here, we summarize the emerging link between O-GlcNAcylation and hepatic pathological processes and provide information about the development of therapeutic strategies for liver diseases.
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