MicroRNA in Fibrotic Disorders: A Potential Target for Future Therapeutics

被引:3
作者
Mehjabin, Aanushka [1 ]
Kabir, Maliha [1 ]
Micolucci, Luigina [2 ]
Akhtar, Most Mauluda [1 ]
Mollah, A. K. M. Moniruzzaman [1 ]
Islam, Md Soriful [3 ]
机构
[1] Asian Univ Women, Sci & Math Program, Chittagong 4000, Bangladesh
[2] Univ Politecn Marche, Dept Clin & Mol Sci, I-60126 Ancona, Italy
[3] Johns Hopkins Med, Dept Gynecol & Obstet, Div Reprod Sci & Womens Hlth Res, Baltimore, MD 21205 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2023年 / 28卷 / 11期
关键词
microRNA; fibrotic disorders; cardiac fibrosis; liver fibrosis; kidney fibrosis; lung fibrosis; dermal fibrosis; primary myelofi-brosis; miRNA therapeutic; natural compounds; REGULATES CARDIAC FIBROSIS; EXTRACELLULAR-MATRIX; MYOCARDIAL FIBROSIS; DOWN-REGULATION; TGF-BETA; LIVER FIBROSIS; RENAL FIBROSIS; NUCLEAR EXPORT; UP-REGULATION; CELL-PROLIFERATION;
D O I
10.31083/j.fbl2811317
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fibrotic disorders are defined by accumulating excessive extracellular matrix (ECM) components, especially collagens, in various organs, leading to tissue scarring and organ dysfunction. These conditions are associated with significant challenges in the healthcare system because of their progressive nature and limited treatment options. MicroRNAs (miRNAs) are small non-coding RNA molecules (approximately 22 nucleotides) that modulate gene expression by selectively targeting mRNAs for degradation or translational repression. MiRNAs have recently been identified as potential targets for therapeutic developments in fibrotic disorders. They play vital roles in inducing fibrotic phenotype by regulating fibroblast activation and ECM remodeling. Multiple strategies for targeting specific miRNAs in fibrotic disorders have been explored, including antisense oligonucleotides, small molecule modulators, and natural compounds. This review discussed the role of miRNAs in different fibrotic disorders, including cardiac fibrosis, liver fibrosis, kidney fibrosis, lung fibrosis, dermal fibrosis, and primary myelofibrosis, with recent advances in developing miRNA-based therapeutics.
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页数:21
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