Your browser doesn't support javascript.
loading
Cardiac splicing as a diagnostic and therapeutic target.
Gotthardt, Michael; Badillo-Lisakowski, Victor; Parikh, Victoria Nicole; Ashley, Euan; Furtado, Marta; Carmo-Fonseca, Maria; Schudy, Sarah; Meder, Benjamin; Grosch, Markus; Steinmetz, Lars; Crocini, Claudia; Leinwand, Leslie.
Afiliação
  • Gotthardt M; Neuromuscular and Cardiovascular Cell Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany. gotthardt@mdc-berlin.de.
  • Badillo-Lisakowski V; DZHK (German Center for Cardiovascular Research Partner Site Berlin), Berlin, Germany. gotthardt@mdc-berlin.de.
  • Parikh VN; Department of Cardiology, Charité - Universitätsmedizin Berlin, Berlin, Germany. gotthardt@mdc-berlin.de.
  • Ashley E; Neuromuscular and Cardiovascular Cell Biology, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Furtado M; DZHK (German Center for Cardiovascular Research Partner Site Berlin), Berlin, Germany.
  • Carmo-Fonseca M; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Palo Alto, CA, USA.
  • Schudy S; Stanford Center for Inherited Cardiovascular Disease, Stanford University School of Medicine, Palo Alto, CA, USA.
  • Meder B; Stanford Genome Technology Center, Stanford University, Palo Alto, CA, USA.
  • Grosch M; Department of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.
  • Steinmetz L; Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
  • Crocini C; Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.
  • Leinwand L; Institute for Cardiomyopathies, Department of Medicine III, University of Heidelberg, Heidelberg, Germany.
Nat Rev Cardiol ; 20(8): 517-530, 2023 Aug.
Article em En | MEDLINE | ID: mdl-36653465
ABSTRACT
Despite advances in therapeutics for heart failure and arrhythmias, a substantial proportion of patients with cardiomyopathy do not respond to interventions, indicating a need to identify novel modifiable myocardial pathobiology. Human genetic variation associated with severe forms of cardiomyopathy and arrhythmias has highlighted the crucial role of alternative splicing in myocardial health and disease, given that it determines which mature RNA transcripts drive the mechanical, structural, signalling and metabolic properties of the heart. In this Review, we discuss how the analysis of cardiac isoform expression has been facilitated by technical advances in multiomics and long-read and single-cell sequencing technologies. The resulting insights into the regulation of alternative splicing - including the identification of cardiac splice regulators as therapeutic targets and the development of a translational pipeline to evaluate splice modulators in human engineered heart tissue, animal models and clinical trials - provide a basis for improved diagnosis and therapy. Finally, we consider how the medical and scientific communities can benefit from facilitated acquisition and interpretation of splicing data towards improved clinical decision-making and patient care.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca / Cardiomiopatias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Cardíaca / Cardiomiopatias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article