The ubiquitin-proteasome system: A potential therapeutic target for heart failure
- PMID: 28341100
- DOI: 10.1016/j.healun.2017.02.012
The ubiquitin-proteasome system: A potential therapeutic target for heart failure
Abstract
The rising incidence of heart failure (HF) is one of the biggest challenges in cardiovascular medicine. The persistent shortage of donor organs for transplantation has led to an expanding application of left ventricular assist devices as a bridge to recovery. Accumulating evidence suggests that the ubiquitin-proteasome system (UPS), which is responsible for protein degradation, plays a direct role in cardiac hypertrophy and HF and is impacted by mechanical unloading. The UPS system also plays a role in the cardiac regulation of apoptosis, cell mass, and sarcomere quality control. Furthermore, it is a key regulator of β2-adrenergic signaling, cell excitability, and conductance. In this review, we discuss the roles of the UPS in cardiac health and disease, including its roles in the pathologic hypertrophy associated with HF and its reversal during mechanical unloading. Finally, we suggest future areas of research, including possible therapeutic strategies for reversing cardiac remodeling by targeting the UPS.
Keywords: LVAD; autophagy; heart failure; proteosome; regenerative medicine.
Copyright © 2017 International Society for the Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.
Similar articles
-
Ventricular unloading is associated with increased 20s proteasome protein expression in the myocardium.J Heart Lung Transplant. 2010 Jan;29(1):125-32. doi: 10.1016/j.healun.2009.07.022. Epub 2009 Oct 17. J Heart Lung Transplant. 2010. PMID: 19837610
-
Mechanical unloading activates FoxO3 to trigger Bnip3-dependent cardiomyocyte atrophy.J Am Heart Assoc. 2013 Apr 8;2(2):e000016. doi: 10.1161/JAHA.113.000016. J Am Heart Assoc. 2013. PMID: 23568341 Free PMC article.
-
The ubiquitin proteasome system in human cardiomyopathies and heart failure.Am J Physiol Heart Circ Physiol. 2013 May 15;304(10):H1283-93. doi: 10.1152/ajpheart.00249.2012. Epub 2013 Mar 11. Am J Physiol Heart Circ Physiol. 2013. PMID: 23479263 Free PMC article. Review.
-
Sent to destroy: the ubiquitin proteasome system regulates cell signaling and protein quality control in cardiovascular development and disease.Circ Res. 2010 Feb 19;106(3):463-78. doi: 10.1161/CIRCRESAHA.109.208801. Circ Res. 2010. PMID: 20167943 Free PMC article. Review.
-
[Congestive heart failure: reverse cardiac remodeling mediated by left ventricular assist devices].Pathologe. 2012 May;33(3):175-82. doi: 10.1007/s00292-011-1559-3. Pathologe. 2012. PMID: 22576594 German.
Cited by
-
RING Finger Protein 10 Regulates AP-1/Meox2 to Mediate Pirarubicin-Induced Cardiomyocyte Apoptosis.Oxid Med Cell Longev. 2023 Jan 20;2023:7872193. doi: 10.1155/2023/7872193. eCollection 2023. Oxid Med Cell Longev. 2023. PMID: 36713029 Free PMC article.
-
Bioinformatic analysis for potential biological processes and key targets of heart failure-related stroke.J Zhejiang Univ Sci B. 2021 Sept 15;22(9):718-732. doi: 10.1631/jzus.B2000544. J Zhejiang Univ Sci B. 2021. PMID: 34514752 Free PMC article.
-
BK Channel Dysfunction in Diabetic Coronary Artery: Role of the E3 Ubiquitin Ligases.Front Physiol. 2020 May 29;11:453. doi: 10.3389/fphys.2020.00453. eCollection 2020. Front Physiol. 2020. PMID: 32547406 Free PMC article. Review.
-
Metabolic Processes are Potential Biological Processes Distinguishing Nonischemic Dilated Cardiomyopathy from Ischemic Cardiomyopathy: A Clue from Serum Proteomics.Pharmgenomics Pers Med. 2021 Sep 16;14:1169-1184. doi: 10.2147/PGPM.S323379. eCollection 2021. Pharmgenomics Pers Med. 2021. PMID: 34557019 Free PMC article.
-
Ubiquitin‑proteasomes are the dominant mediators of the regulatory effect of microRNA‑1 on cardiac remodeling after myocardial infarction.Int J Mol Med. 2019 Nov;44(5):1899-1907. doi: 10.3892/ijmm.2019.4330. Epub 2019 Sep 4. Int J Mol Med. 2019. PMID: 31485642 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous