Emerging epigenetic therapies of cardiac fibrosis and remodelling in heart failure: from basic mechanisms to early clinical development

Author:

McKinsey Timothy A1,Foo Roger23ORCID,Anene-Nzelu Chukwuemeka George234,Travers Joshua G1,Vagnozzi Ronald J1,Weber Natalie5,Thum Thomas567ORCID

Affiliation:

1. Department of Medicine, Division of Cardiology, and Consortium for Fibrosis Research & Translation, University of Colorado Anschutz Medical Campus , 12700 E.19th Ave, Aurora, CO, 80045-2507 , USA

2. NUHS Cardiovascular Disease Translational Research Programme, NUS Yong Loo Lin School of Medicine , 14 Medical Drive, Level 8, 117599 Singapore , Singapore

3. Cardiovascular Research Institute, National University Heart Centre , 14 Medical Drive, Level 8, 117599 Singapore , Singapore

4. Montreal Heart Institute , 5000 Rue Belanger, H1T 1C8, Montreal, Canada

5. Institute of Molecular and Translational Therapeutic Strategies (IMTTS), Hannover Medical School, Carl-Neuberg-Straße 1, 30625   Hannover , Germany

6. REBIRTH Center for Translational Regenerative Therapies, Hannover Medical School, Carl-Neuberg-Straße 1, 30625   Hannover , Germany

7. Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Straße 1, 30625   Hannover , Germany

Abstract

Abstract Cardiovascular diseases and specifically heart failure (HF) impact global health and impose a significant economic burden on society. Despite current advances in standard of care, the risks for death and readmission of HF patients remain unacceptably high and new therapeutic strategies to limit HF progression are highly sought. In disease settings, persistent mechanical or neurohormonal stress to the myocardium triggers maladaptive cardiac remodelling, which alters cardiac function and structure at both the molecular and cellular levels. The progression and magnitude of maladaptive cardiac remodelling ultimately leads to the development of HF. Classical therapies for HF are largely protein-based and mostly are targeted to ameliorate the dysregulation of neuroendocrine pathways and halt adverse remodelling. More recently, investigation of novel molecular targets and the application of cellular therapies, epigenetic modifications, and regulatory RNAs has uncovered promising new avenues to address HF. In this review, we summarize the current knowledge on novel cellular and epigenetic therapies and focus on two non-coding RNA-based strategies that reached the phase of early clinical development to counteract cardiac remodelling and HF. The current status of the development of translating those novel therapies to clinical practice, limitations, and future perspectives are additionally discussed.

Funder

National Institutes of Health

American Heart Association

ERC Advanced Grant REVERSE

Singapore National Medical Research Council

Biomedical Research Council

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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