长非编码 RNA MEG3:纤维化的积极参与者。

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacological Reports Pub Date : 2024-10-07 DOI:10.1007/s43440-024-00661-x
Xiaoying Jiang
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引用次数: 0

摘要

纤维化的特点是细胞外基质成分的过度积累,它会破坏正常的组织结构并导致器官功能障碍。长非编码 RNA(lncRNA)是长于 200 个核苷酸的 RNA 子集,它们不会转化为蛋白质。越来越多的研究表明,lncRNA 母系表达基因 3(MEG3)在多个组织纤维化的病理过程中出现失调。研究发现,LncRNA MEG3可调控靶蛋白的表达,或作为miRNAs海绵控制纤维化的发展,参与NF-ҡB、PI3K/AKT、JAK2/STAT3、Wnt/β-catenin、ERK/p38和Hh通路。重要的是,干扰 MEG3 水平可改善纤维化。本综述总结了现有的关于lncRNA MEG3在纤维化中的作用的研究,有助于深入了解MEG3在纤维化中的作用。
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Long noncoding RNA MEG3: an active player in fibrosis.

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-ҡB, PI3K/AKT, JAK2/STAT3, Wnt/β-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.

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来源期刊
Pharmacological Reports
Pharmacological Reports 医学-药学
CiteScore
8.40
自引率
0.00%
发文量
91
审稿时长
6 months
期刊介绍: Pharmacological Reports publishes articles concerning all aspects of pharmacology, dealing with the action of drugs at a cellular and molecular level, and papers on the relationship between molecular structure and biological activity as well as reports on compounds with well-defined chemical structures. Pharmacological Reports is an open forum to disseminate recent developments in: pharmacology, behavioural brain research, evidence-based complementary biochemical pharmacology, medicinal chemistry and biochemistry, drug discovery, neuro-psychopharmacology and biological psychiatry, neuroscience and neuropharmacology, cellular and molecular neuroscience, molecular biology, cell biology, toxicology. Studies of plant extracts are not suitable for Pharmacological Reports.
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