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Updated: Mar 10, 2026

Development of an In Vitro Assay to Evaluate Contractile Function of Mesenchymal Cells that Underwent Epithelial-Mesenchymal Transition
Published on: June 10, 2016
MicroRNAs-mediated epithelial-mesenchymal transition in fibrotic diseases
Xiao-Zhou Zou1, Ting Liu1, Zhi-Cheng Gong2
1Department of Pharmacology, Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, Hunan 410078, China.
Abstract:
MicroRNAs (miRNAs), a large family of small and highly conserved non-coding RNAs, regulate gene expression through translational repression or mRNA degradation. Aberrant expression of miRNAs underlies a spectrum of diseases including organ fibrosis. Recent evidence suggests that miRNAs contribute to organ fibrosis through mediating epithelial-mesenchymal transition (EMT). Alleviation of EMT has been proposed as a promising strategy against fibrotic diseases given the key role of EMT in fibrosis. miRNAs impact the expression of specific ligands, receptors, and signaling pathways, thus modulating EMT and consequently influencing fibrosis. This review summarizes the current knowledge concerning how miRNAs regulate EMT and highlights the specific roles that miRNAs-regulated EMT plays in fibrotic diseases as diverse as pulmonary fibrosis, hepatic fibrosis, renal fibrosis and cardiac fibrosis. It is desirable that a more comprehensive understanding of the functions of miRNAs-regulated EMT will facilitate the development of novel diagnostic and therapeutic strategies for various debilitating organ fibrosis.
Insights
MicroRNAs (miRNAs) regulate gene expression and are implicated in organ fibrosis by mediating epithelial-mesenchymal transition (EMT). Understanding miRNA-regulated EMT offers new diagnostic and therapeutic avenues for fibrotic diseases.
Area of Science:
- Molecular Biology
- Genetics
- Pathology
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs regulating gene expression.
- Aberrant miRNA expression is linked to various diseases, including organ fibrosis.
- miRNAs are increasingly recognized for their role in mediating epithelial-mesenchymal transition (EMT), a key process in fibrosis.
Purpose of the Study:
- To review the current understanding of how miRNAs regulate EMT.
- To highlight the specific roles of miRNA-regulated EMT in diverse fibrotic diseases.
- To underscore the potential of targeting miRNA-regulated EMT for therapeutic development.
Main Methods:
- Literature review of studies on miRNAs, EMT, and organ fibrosis.
- Synthesis of evidence linking miRNA function to EMT pathways.
- Analysis of miRNA involvement across different fibrotic conditions (pulmonary, hepatic, renal, cardiac).
Main Results:
- miRNAs modulate EMT by affecting ligands, receptors, and signaling pathways.
- miRNA-regulated EMT is a significant contributor to pulmonary, hepatic, renal, and cardiac fibrosis.
- Specific miRNAs have been identified that promote or inhibit EMT in fibrotic contexts.
Conclusions:
- miRNA-regulated EMT is a critical mechanism in the pathogenesis of organ fibrosis.
- Targeting specific miRNAs or their downstream effects on EMT presents a promising therapeutic strategy.
- Further research into miRNA-regulated EMT could lead to novel diagnostic and therapeutic tools for fibrotic diseases.
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