Matrix metalloproteinases in coronary artery disease and myocardial infarction.
Hanna BräuningerSaskia KrügerLucas BacmeisterAlexander NyströmKilian EyerichDirk WestermannDiana LindnerPublished in: Basic research in cardiology (2023)
Cardiovascular diseases (CVDs) remain the leading cause of death worldwide. Most cardiovascular deaths are caused by ischaemic heart diseases such as myocardial infarction (MI). Hereby atherosclerosis in the coronary arteries often precedes disease manifestation. Since tissue remodelling plays an important role in the development and progression of atherosclerosis as well as in outcome after MI, regulation of matrix metalloproteinases (MMPs) as the major ECM-degrading enzymes with diverse other functions is crucial. Here, we provide an overview of the expression profiles of MMPs in coronary artery and left ventricular tissue using publicly available data from whole tissue to single-cell resolution. To approach an association between MMP expression and the development and outcome of CVDs, we further review studies investigating polymorphisms in MMP genes since polymorphisms are known to have an impact on gene expression. This review therefore aims to shed light on the role of MMPs in atherosclerosis and MI by summarizing current knowledge from publically available datasets, human studies, and analyses of polymorphisms up to preclinical and clinical trials of pharmacological MMP inhibition.
Keyphrases
- left ventricular
- coronary artery
- cardiovascular disease
- coronary artery disease
- gene expression
- heart failure
- clinical trial
- single cell
- endothelial cells
- poor prognosis
- rna seq
- cell migration
- healthcare
- dna methylation
- aortic stenosis
- cardiovascular events
- cardiac resynchronization therapy
- mitral valve
- atrial fibrillation
- cell therapy
- stem cells
- percutaneous coronary intervention
- phase ii
- left atrial
- case control
- long non coding rna
- artificial intelligence
- mesenchymal stem cells
- transcription factor
- phase iii
- double blind
- genome wide identification
- pulmonary hypertension
- induced pluripotent stem cells