| Literature DB >> 32638021 |
Christian Bär1,2, Shambhabi Chatterjee1,2, Inês Falcão Pires3, Patrícia Rodrigues3, Joost P G Sluijter4, Reinier A Boon5,6,7, Rosa M Nevado8,9, Vicente Andrés8,9, Marida Sansonetti1,2,10,11, Leon de Windt10,11, Michele Ciccarelli12, Nazha Hamdani13,14, Stephane Heymans15,16, Raquel Figuinha Videira3,10,11, Carlo G Tocchetti17, Mauro Giacca18,19,20, Serena Zacchigna18,20, Stefan Engelhardt21,22, Stefanie Dimmeler23,24,25, Rosalinda Madonna26,27, Thomas Thum1,2.
Abstract
Vast parts of mammalian genomes are actively transcribed, predominantly giving rise to non-coding RNA (ncRNA) transcripts including microRNAs, long ncRNAs, and circular RNAs among others. Contrary to previous opinions that most of these RNAs are non-functional molecules, they are now recognized as critical regulators of many physiological and pathological processes including those of the cardiovascular system. The discovery of functional ncRNAs has opened up new research avenues aiming at understanding ncRNA-related disease mechanisms as well as exploiting them as novel therapeutics in cardiovascular therapy. In this review, we give an update on the current progress in ncRNA research, particularly focusing on cardiovascular physiological and disease processes, which are under current investigation at the ESC Working Groups of Myocardial Function and Cellular Biology of the Heart. This includes a range of topics such as extracellular vesicle-mediated communication, neurohormonal regulation, inflammation, cardiac remodelling, cardio-oncology as well as cardiac development and regeneration, collectively highlighting the wide-spread involvement and importance of ncRNAs in the cardiovascular system. Published on behalf of the European Society of Cardiology. All rights reserved.Entities:
Keywords: Aging; Cardiovascular disease; MicroRNA; Non-coding RNA; Non-coding RNA therapy; Regeneration; Remodelling
Year: 2020 PMID: 32638021 DOI: 10.1093/cvr/cvaa195
Source DB: PubMed Journal: Cardiovasc Res ISSN: 0008-6363 Impact factor: 10.787