| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10953739 | Journal of Molecular and Cellular Cardiology | 2015 | 9 Pages | 
Abstract
												Cardiovascular diseases are currently the main cause of morbidity and mortality worldwide. Ischemic heart disease, in particular, is responsible for the majority of cardiac-related deaths. Given the negligible regenerative potential of the human myocardium, there is a strong need for therapeutic strategies aiming at enhancing cardiomyocyte survival and proliferation following injury or at inhibiting their death. MicroRNAs (miRNAs) are small non-coding RNA molecules regulating gene expression at a post-transcriptional level with important functions in cardiovascular physiology and disease. It has been demonstrated that miRNAs can influence the ability of cardiomyocytes to enter the cell cycle and/or escape from death pathways. Additionally, long non coding-RNAs could be involved in such pathways. This review summarizes recent evidences on noncoding RNAs regulating proliferation and death of cardiomyocytes representing a future therapeutic for the treatment of heart diseases. This article is part of a Special Issue entitled SI: Non-coding RNAs.
											Keywords
												EPCsATG9tuberous sclerosis complex 1mTORC2TSC1VSMCsATG5mTORC1HCMMfn1BCL2/adenovirus E1B 19 kDa protein-interacting protein 3BNIP3AAVMPTPCSCslncRNAmTORmiRNAsI/Rlong non-coding RNAMyocardial infarctionAutophagymitochondrial permeability transition poreischemia/reperfusionProliferationTriiodothyronineApoptosisDiabetes mellitusmicroRNAsapoptosis repressor with caspase recruitment domainCardiac stem cellsVascular smooth muscle cellsEndothelial progenitor cellsCardiomyocyteArcLADLow-density lipoproteinLDLmitofusin 1Necrosismammalian target of rapamycinMammalian target of rapamycin complex 2Mammalian target of rapamycin complex 1Adeno-associated virusleft anterior descending coronary arteryHypertrophic cardiomyopathyCARL
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											Authors
												Maria-Teresa Piccoli, Shashi Kumar Gupta, Thomas Thum, 
											