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Updated: May 7, 2026

MicroRNA In situ Hybridization for Formalin Fixed Kidney Tissues
Published on: November 30, 2013
MicroRNAs in kidney fibrosis and diabetic nephropathy: roles on EMT and EndMT
Swayam Prakash Srivastava1, Daisuke Koya, Keizo Kanasaki
1Department of Diabetology & Endocrinology, Kanazawa Medical University, Uchinada, Ishikawa 920-0293, Japan.
Abstract:
MicroRNAs (miRNAs) are a family of small, noncoding RNAs that regulate gene expression in diverse biological and pathological processes, including cell proliferation, differentiation, apoptosis, and carcinogenesis. As a result, miRNAs emerged as major area of biomedical research with relevance to kidney fibrosis. Fibrosis is characterized by the excess deposition of extracellular matrix (ECM) components, which is the end result of an imbalance of metabolism of the ECM molecule. Recent evidence suggests that miRNAs participate in the fibrotic process in a number of organs including the heart, kidney, liver, and lung. Epithelial mesenchymal transition (EMT) and endothelial mesenchymal transition (EndMT) programs play vital roles in the development of fibrosis in the kidney. A growing number of the extracellular and intracellular molecules that control EMT and EndMT have been identified and could be exploited in developing therapeutics for fibrosis. This review highlights recent advances on the role of miRNAs in the kidney diseases; diabetic nephropathy especially focused on EMT and EndMT program responsible for the development of kidney fibrosis. These miRNAs can be utilized as a potential novel drug target for the studying of underlying mechanism and treatment of kidney fibrosis.
Insights
MicroRNAs (miRNAs) regulate gene expression and are key in kidney fibrosis. Targeting these small RNAs offers a promising therapeutic strategy for kidney diseases like diabetic nephropathy.
Area of Science:
- Biomedical research
- Molecular biology
- Nephrology
Background:
- MicroRNAs (miRNAs) are small, noncoding RNAs regulating gene expression in biological and pathological processes.
- Kidney fibrosis involves excessive extracellular matrix deposition due to ECM metabolism imbalance.
- miRNAs are implicated in fibrotic processes across multiple organs, including the kidney.
Purpose of the Study:
- To review recent advances on the role of miRNAs in kidney diseases, particularly diabetic nephropathy.
- To focus on the epithelial-mesenchymal transition (EMT) and endothelial-mesenchymal transition (EndMT) programs in kidney fibrosis development.
- To highlight miRNAs as potential therapeutic targets for kidney fibrosis.
Main Methods:
- Literature review of recent advances in miRNA research related to kidney fibrosis.
- Focus on studies investigating the role of miRNAs in EMT and EndMT pathways.
- Analysis of current understanding of miRNA involvement in diabetic nephropathy and kidney fibrosis.
Main Results:
- miRNAs play significant roles in regulating gene expression relevant to kidney fibrosis.
- EMT and EndMT programs are critical in the pathogenesis of kidney fibrosis.
- Numerous extracellular and intracellular molecules controlling EMT and EndMT have been identified.
Conclusions:
- miRNAs are crucial regulators in kidney fibrosis, particularly in diabetic nephropathy.
- Targeting specific miRNAs involved in EMT and EndMT presents a novel therapeutic avenue.
- Further research into miRNA mechanisms can lead to effective treatments for kidney fibrosis.
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