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Epigenomic and transcriptomic approaches in the post-genomic era : Path to novel targets for diagnosis and therapy of the ischaemic heart? Position Paper of the European Society of Cardiology Working Group on Cellular Biology of the Heart
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Publication Volume
Publication Issue
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Authors
Perrino, Cinzia
Barabási, Albert László
Condorelli, Gianluigi
Davidson, Sean Michael
De Windt, Leon
Dimmeler, Stefanie
Engel, Felix Benedikt
Hausenloy, Derek John
Hill, Joseph Addison
Van Laake, Linda Wilhelmina
Lecour, Sandrine
Leor, Jonathan
Madonna, Rosalinda
Mayr, Manuel
Prunier, Fabrice
Sluijter, Joost Petrus Geradus
Schulz, Rainer
Thum, Thomas
Ytrehus, Kirsti
Ferdinandy, Péter
Barabási, Albert László
Condorelli, Gianluigi
Davidson, Sean Michael
De Windt, Leon
Dimmeler, Stefanie
Engel, Felix Benedikt
Hausenloy, Derek John
Hill, Joseph Addison
Van Laake, Linda Wilhelmina
Lecour, Sandrine
Leor, Jonathan
Madonna, Rosalinda
Mayr, Manuel
Prunier, Fabrice
Sluijter, Joost Petrus Geradus
Schulz, Rainer
Thum, Thomas
Ytrehus, Kirsti
Ferdinandy, Péter
Editors
Keywords
Big Data
Bioinformatics
Multiomics
Network analysis
Omics
Tailored medicine
General Medicine
SDG 3 - Good Health and Well-being
Bioinformatics
Multiomics
Network analysis
Omics
Tailored medicine
General Medicine
SDG 3 - Good Health and Well-being
URI
https://hdl.handle.net/20.500.14018/27164
Abstract
Despite advances in myocardial reperfusion therapies, acute myocardial ischaemia/reperfusion injury and consequent ischaemic heart failure represent the number one cause of morbidity and mortality in industrialized societies. Although different therapeutic interventions have been shown beneficial in preclinical settings, an effective cardioprotective or regenerative therapy has yet to be successfully introduced in the clinical arena. Given the complex pathophysiology of the ischaemic heart, large scale, unbiased, global approaches capable of identifying multiple branches of the signalling networks activated in the ischaemic/reperfused heart might be more successful in the search for novel diagnostic or therapeutic targets. High-throughput techniques allow high-resolution, genome-wide investigation of genetic variants, epigenetic modifications, and associated gene expression profiles. Platforms such as proteomics and metabolomics (not described here in detail) also offer simultaneous readouts of hundreds of proteins and metabolites. Isolated omics analyses usually provide Big Data requiring large data storage, advanced computational resources and complex bioinformatics tools. The possibility of integrating different omics approaches gives new hope to better understand the molecular circuitry activated by myocardial ischaemia, putting it in the context of the human ‘diseasome’. Since modifications of cardiac gene expression have been consistently linked to pathophysiology of the ischaemic heart, the integration of epigenomic and transcriptomic data seems a promising approach to identify crucial disease networks. Thus, the scope of this Position Paper will be to highlight potentials and limitations of these approaches, and to provide recommendations to optimize the search for novel diagnostic or therapeutic targets for acute ischaemia/reperfusion injury and ischaemic heart failure in the post-genomic era.
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Place of Publication
Type
Journal article
Date
2017-06-01
Language
ISBN
Identifiers
10.1093/cvr/cvx070