The function of miR-143, miR-145 and the MiR-143 host gene in cardiovascular development and disease

Francesca Vacante, Laura Denby, Judith C. Sluimer, Andrew H. Baker*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

47 Citations (Web of Science)

Abstract

Noncoding RNAs (long noncoding RNAs and small RNAs) are emerging as critical modulators of phenotypic changes associated with physiological and pathological contexts in a variety of cardiovascular diseases (CVDs). Although it has been well established that hereditable genetic alterations and exposure to risk factors are crucial in the development of CVDs, other critical regulators of cell function impact on disease processes. Here we discuss noncoding RNAs have only recently been identified as key players involved in the progression of disease. In particular, we discuss micro RNA (miR)-143/145 since they represent one of the most characterised microRNA clusters regulating smooth muscle cell (SMC) differentiation and phenotypic switch in response to vascular injury and remodelling. MiR143HG is a well conserved long noncoding RNA (lncRNA), which is the host gene for miR-143/145 and recently implicated in cardiac specification during heart development. Although the lncRNA-miRNA interactions have not been completely characterised, their crosstalk is now beginning to emerge and likely requires further research focus. In this review we give an overview of the biology of the genomic axis that is miR-143/145 and MiR143HG, focusing on their important functional role(s) in the cardiovascular system.

Original languageEnglish
Pages (from-to)24-30
Number of pages7
JournalVascular Pharmacology
Volume112
DOIs
Publication statusPublished - Jan 2019

Keywords

  • LONG NONCODING RNAS
  • SMOOTH-MUSCLE-CELLS
  • ENDOTHELIAL-CELLS
  • MICRORNA
  • EXPRESSION
  • BIOGENESIS
  • PHENOTYPE
  • SIGNATURE
  • GENOMICS
  • MICROVESICLES

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