Identification of Long Noncoding RNA H19 as a New Biomarker and Therapeutic Target in Right Ventricular Failure in Pulmonary Arterial Hypertension.

Abstract

BACKGROUND:

Right ventricular (RV) function is the major determinant for both functional capacity and survival in patients with pulmonary arterial hypertension (PAH). Despite the recognized clinical importance of preserving RV function, the subcellular mechanisms that govern the transition from a compensated to a decompensated state remain poorly understood and as a consequence there are no clinically established treatments for RV failure and a paucity of clinically useful biomarkers. Accumulating evidence indicates that long noncoding RNAs are powerful regulators of cardiac development and disease. Nonetheless, their implication in adverse RV remodeling in PAH is unknown.

METHODS:

Expression of the long noncoding RNA H19 was assessed by quantitative PCR in plasma and RV from patients categorized as control RV, compensated RV or decompensated RV based on clinical history and cardiac index. The impact of H19 suppression using GapmeR was explored in 2 rat models mimicking RV failure, namely the monocrotaline and pulmonary artery banding. Echocardiographic, hemodynamic, histological, and biochemical analyses were conducted. In vitro gain- and loss-of-function experiments were performed in rat cardiomyocytes.

RESULTS:

We demonstrated that H19 is upregulated in decompensated RV from PAH patients and correlates with RV hypertrophy and fibrosis. Similar findings were observed in monocrotaline and pulmonary artery banding rats. We found that silencing H19 limits pathological RV hypertrophy, fibrosis and capillary rarefaction, thus preserving RV function in monocrotaline and pulmonary artery banding rats without affecting pulmonary vascular remodeling. This cardioprotective effect was accompanied by E2F transcription factor 1-mediated upregulation of enhancer of zeste homolog 2. In vitro, knockdown of H19 suppressed cardiomyocyte hypertrophy induced by phenylephrine, while its overexpression has the opposite effect. Finally, we demonstrated that circulating H19 levels in plasma discriminate PAH patients from controls, correlate with RV function and predict long-term survival in 2 independent idiopathic PAH cohorts. Moreover, H19 levels delineate subgroups of patients with differentiated prognosis when combined with the NT-proBNP (N-terminal pro-B-type natriuretic peptide) levels or the risk score proposed by both REVEAL (Registry to Evaluate Early and Long-Term PAH Disease Management) and the 2015 European Pulmonary Hypertension Guidelines.

CONCLUSIONS:

Our findings identify H19 as a new therapeutic target to impede the development of maladaptive RV remodeling and a promising biomarker of PAH severity and prognosis.

• Authors: Junichi Omura, Karima Habbout, Tsukasa Shimauchi, Wen-Hui Wu, Sandra Breuils-Bonnet, Eve Tremblay, Sandra Martineau, Valérie Nadeau, Kassandra Gagnon, Florence Mazoyer, Jean Perron, Francois Potus, Jian-Hui Lin, Hamza Zafar, David G Kiely, Allan Lawrie, Stephen L Archer, Roxane Paulin, Steeve Provencher, Olivier Boucherat, Sébastien Bonnet
• Journal: Circulation (Circulation) Vol. 142 Issue 15 Pg. 1464-1484 (10 13 2020) ISSN: 1524-4539 [Electronic] United States
• PMID: 32698630 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Biomarkers
• H19 long non-coding RNA
• Peptide Fragments
• RNA, Long Noncoding
• pro-brain natriuretic peptide (1-76)
• Natriuretic Peptide, Brain

Topics

• Animals
• Biomarkers (metabolism)
• Heart Failure (metabolism, mortality, pathology)
• Humans
• Natriuretic Peptide, Brain (metabolism)
• Peptide Fragments (metabolism)
• Pulmonary Arterial Hypertension (metabolism, mortality, pathology)
• RNA, Long Noncoding (metabolism)
• Rats
• Vascular Remodeling
• Ventricular Dysfunction, Right (metabolism, mortality, pathology)