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.

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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