Noncoding RNAs in peritoneal fibrosis: Background, Mechanism, and Therapeutic Approach

Biomed Pharmacother. 2020 Sep:129:110385. doi: 10.1016/j.biopha.2020.110385. Epub 2020 Jul 2.

Abstract

Peritoneal fibrosis (PF) is the main reason for patients to withdraw from peritoneal dialysis, while the mechanism underlying PF remains unclear. Increasing evidence has demonstrated the regulatory roles of different classes of noncoding RNAs (ncRNAs) in PF. MicroRNAs (miRNAs), which belong to a distinct class of ncRNAs, play crucial roles in the post-transcriptional regulation of gene expression. Studies have suggested that miRNAs play important roles in the pathogenesis of PF and have the potential to be used as diagnostic markers and therapeutic targets for PF in the future. Long noncoding RNAs (lncRNAs) have raised much attention in the recent years, which are involved in the pathophysiological processes of many diseases, including tumors, heart diseases and so on. Recently, some researchers have begun to notice the roles of lncRNAs in PF, and found that lncRNAs play certain roles in the pathogenesis of PF. Circular RNAs (circRNAs) have been proven to be participated in the pathogenesis of many diseases, including tumor metastasis, organ fibrosis and so on. However, studies on the correlation of circRNAs and PF are rather poor compared with miRNAs and lncRNAs. In this review, we will focus on the findings of ncRNAs in peritoneal dialysis therapy and discuss the rising interests in ncRNAs as diagnostic and therapeutic targets of PF.

Keywords: Circular RNA; Long noncoding RNAs; Peritoneal fibrosis; microRNA.

Publication types

  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation
  • Humans
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Peritoneal Dialysis / adverse effects*
  • Peritoneal Fibrosis / etiology
  • Peritoneal Fibrosis / genetics
  • Peritoneal Fibrosis / metabolism*
  • Peritoneal Fibrosis / pathology
  • Peritoneum / metabolism*
  • Peritoneum / pathology
  • RNA, Circular / genetics
  • RNA, Circular / metabolism*
  • Signal Transduction

Substances

  • MicroRNAs
  • RNA, Circular