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Micro-RNA Analysis in Pulmonary Arterial Hypertension: Current Knowledge and Challenges
Cátia A Santos-Ferreira1,2, Mónica T Abreu3,4,2, Carla I Marques3,4,2
1Cardiology Department, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
JACC. Basic to Translational Science
|December 9, 2020
Summary
This review explores micro-RNA (miRNA) deregulation in pulmonary arterial hypertension (PAH), highlighting four key miRNAs (miR-29, miR-124, miR-140, miR-204) with significant translational potential for treating this rare vascular disease.
Area of Science:
- Cardiovascular Research
- Molecular Biology
- Genetics
Background:
- Pulmonary arterial hypertension (PAH) is a severe, chronic vascular disease with limited treatment options.
- Micro-RNAs (miRNAs) play a crucial role in the multifactorial pathogenesis of PAH through gene expression regulation.
- The rapidly evolving field of miRNA research in PAH presents challenges in identifying therapeutically relevant targets.
Purpose of the Study:
- To review current knowledge on miRNA expression profiles in pulmonary arterial hypertension.
- To discuss the analytical and interpretative challenges in studying miRNAs in PAH.
- To identify and highlight specific miRNAs with high translational potential for PAH therapeutics.
Main Methods:
- Comprehensive literature review of studies investigating miRNA expression in PAH.
- Analysis of existing data on miRNA deregulation in pulmonary arterial hypertension.
- Identification of miRNAs consistently implicated in PAH pathogenesis and progression.
Main Results:
- miRNA expression is significantly altered in patients with pulmonary arterial hypertension.
- Specific miRNAs, including miR-29, miR-124, miR-140, and miR-204, show promise due to their roles in PAH.
- Challenges in miRNA detection and functional validation impact translational efforts.
Conclusions:
- miRNA deregulation is a key feature of pulmonary arterial hypertension pathogenesis.
- miR-29, miR-124, miR-140, and miR-204 represent promising therapeutic targets for PAH.
- Further research is needed to overcome analytical hurdles and advance miRNA-based PAH treatments.
Keywords:
BMPR2, bone morphogenetic protein receptor type 2EPC, endothelial progenitor cellHIF, hypoxia-inducible factorHPAH, hereditary pulmonary arterial hypertensionMCT, monocrotalinePAAF, pulmonary arterial adventitial fibroblastPAEC, pulmonary artery endothelial cellPAH, pulmonary arterial hypertensionPASMC, pulmonary artery smooth muscle cellsPH, pulmonary hypertensionRV, right ventricleSU/Hx/Nx, association of Sugen 5416 with chronic hypoxia followed by normoxiaWHO, World Health Organizationanimal modellncRNA, long noncoding RNAmRNA, messenger RNAmiRNA, micro-RNAmicro-RNAmicroarrayncRNAs, noncoding RNAspulmonary arterial hypertension
