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Published on: June 14, 2016
Cardiac fibrosis: emerging agents in preclinical and clinical development
Roberto Spoladore1, Giulio Falasconi2, Giorgio Fiore2
1Cardiology Division, Alessandro Manzoni Hospital, ASST-Lecco , Italy.
Introduction:
Myocardial fibrosis is a remarkably dynamic process mediated by different molecular pathways that represent potential targets of novel therapeutic interventions. Transforming Growth Factor-beta (TGF-β), connective Tissue Growth Factor (cTGF) and Galectin-3 (Gal-3) represent the most promising targets on which research has been currently focusing.
Area Covered:
This review initially discusses those drugs used in clinical practice for their anti-fibrotic properties and later examines emerging pathway-specific agents in preclinical and clinical development [phase I and II-concluded or ongoing trials]. We performed a PubMed, Embase and Google Scholar research including original articles, systematic reviews, ongoing and completed trials using combinations of keywords such as 'myocardial fibrosis', 'reverse remodeling', 'RAAs', 'therapy'.
Expert Opinion:
A variety of preclinical evidences suggest that new drugs and molecules are potentially useful to target cardiac fibrosis and improve left ventricular function, reduce infarct size and scars, delay incident heart failure and cardiac dysfunction in animal models. However, there are very few clinical trials investigating the effect of such drugs in this setting, as well as a lack of new engineered molecules for specific targets.
Insights
Novel therapies targeting cardiac fibrosis show promise in preclinical models, but clinical trials are scarce. Further research is needed to validate these anti-fibrotic drugs for treating heart conditions.
Area of Science:
- Cardiovascular Research
- Pharmacology
- Fibrosis Mechanisms
Background:
- Myocardial fibrosis is a dynamic process with therapeutic potential.
- Transforming Growth Factor-beta (TGF-β), connective Tissue Growth Factor (cTGF), and Galectin-3 (Gal-3) are key targets.
- Research focuses on novel therapeutic interventions for cardiac fibrosis.
Purpose of the Study:
- To review current drugs with anti-fibrotic properties.
- To examine emerging pathway-specific agents in development.
- To assess the clinical and preclinical status of cardiac fibrosis therapies.
Main Methods:
- Literature search of PubMed, Embase, and Google Scholar.
- Included original articles, systematic reviews, and clinical trials.
- Used keywords: 'myocardial fibrosis', 'reverse remodeling', 'RAAs', 'therapy'.
Main Results:
- Preclinical evidence supports new drugs for cardiac fibrosis.
- Potential benefits include improved left ventricular function and reduced infarct size.
- Few clinical trials exist for these novel anti-fibrotic agents.
Conclusions:
- New drugs show potential in animal models for cardiac fibrosis.
- Clinical investigation of these agents is limited.
- A need exists for engineered molecules targeting specific fibrosis pathways.
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