MicroRNAs in pulmonary arterial hypertension.

Abstract:

:Pulmonary arterial hypertension (PAH) is a devastating disease without effective treatment. Despite decades of research and the development of novel treatments, PAH remains a fatal disease, suggesting an urgent need for better understanding of the pathogenesis of PAH. Recent studies suggest that microRNAs (miRNAs) are dysregulated in patients with PAH and in experimental pulmonary hypertension. Furthermore, normalization of a few miRNAs is reported to inhibit experimental pulmonary hypertension. We have reviewed the current knowledge about miRNA biogenesis, miRNA expression pattern, and their roles in regulation of pulmonary artery smooth muscle cells, endothelial cells, and fibroblasts. We have also identified emerging trends in our understanding of the role of miRNAs in the pathogenesis of PAH and propose future studies that might lead to novel therapeutic strategies for the treatment of PAH.

authors

Zhou G,Chen T,Raj JU

doi

10.1165/rcmb.2014-0166TR

subject

Has Abstract

pub_date

2015-02-01 00:00:00

pages

139-51

issue

2

eissn

1044-1549

issn

1535-4989

journal_volume

52

pub_type

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