Long noncoding RNA MEG3: an active player in fibrosis

被引:0
|
作者
Jiang, Xiaoying [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Hlth Sci Ctr, 76 Yanta West Rd, Xian 710061, Shaanxi, Peoples R China
基金
美国国家科学基金会;
关键词
Fibrosis; Long noncoding RNAs; MEG3; Potential target; STELLATE CELLS ACTIVATION; DIABETIC-NEPHROPATHY; CARDIAC FIBROSIS;
D O I
10.1007/s43440-024-00661-x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fibrosis, characterized by excess accumulation of extracellular matrix components, disrupts normal tissue structure and causes organ dysfunction. Long noncoding RNAs (lncRNAs) are a subset of RNAs longer than 200 nucleotides that are not converted into proteins. The increasing research indicated that lncRNA maternally expressed gene 3 (MEG3) was dysregulated in the pathologic process of fibrosis in several tissues. LncRNA MEG3 was revealed to regulate the expression of target proteins or serve as a miRNAs sponge to control the development of fibrosis, which was involved in NF-kappa B, PI3K/AKT, JAK2/STAT3, Wnt/beta-catenin, ERK/p38, and Hh pathway. Importantly, the interference of MEG3 level ameliorated fibrosis. The present review summarized available studies of lncRNA MEG3 in fibrosis, which is helpful for a deeper understanding of the roles of MEG3 in fibrosis.
引用
收藏
页码:21 / 30
页数:10
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