Non-coding RNAs as therapeutic targets for preventing myocardial ischemia-reperfusion injury
- PMID: 29417868
- DOI: 10.1080/14728222.2018.1439015
Non-coding RNAs as therapeutic targets for preventing myocardial ischemia-reperfusion injury
Abstract
New treatments are required to improve clinical outcomes in patients with acute myocardial infarction (AMI), for reduction of myocardial infarct (MI) size and preventing heart failure. Following AMI, acute ischemia/reperfusion injury (IRI) ensues, resulting in cardiomyocyte death and impaired cardiac function. Emerging studies have implicated a fundamental role for non-coding RNAs (microRNAs [miRNA], and more recently long non-coding RNAs [lncRNA]) in the setting of acute myocardial IRI. Areas covered: In this article, we discuss the roles of miRNAs and lncRNAs as potential biomarkers and therapeutic targets for the detection and treatment of AMI, review their roles as mediators and effectors of cardioprotection, particularly in the settings of interventions such as ischemic pre- and post-conditioning (IPC & IPost) as well as remote ischemic conditioning (RIC), and highlight future strategies for targeting ncRNAs to reduce MI size and prevent heart failure following AMI. Expert opinion: Investigating the roles of miRNAs and lncRNAs in the setting of AMI has provided new insights into the pathophysiology underlying acute myocardial IRI, and has identified novel biomarkers and therapeutic targets for detecting and treating AMI. Pharmacological and genetic manipulation of these ncRNAs has the therapeutic potential to improve clinical outcomes in AMI patients.
Keywords: Ischemia-reperfusion injury; acute myocardial infarction; cardioprotection; ischemic conditioning; long non-coding RNA; microRNAs; non-coding RNAs.
Similar articles
-
Non-Coding RNAs: Prevention, Diagnosis, and Treatment in Myocardial Ischemia-Reperfusion Injury.Int J Mol Sci. 2022 Mar 1;23(5):2728. doi: 10.3390/ijms23052728. Int J Mol Sci. 2022. PMID: 35269870 Free PMC article. Review.
-
Inhibition of the LncRNA Gpr19 attenuates ischemia-reperfusion injury after acute myocardial infarction by inhibiting apoptosis and oxidative stress via the miR-324-5p/Mtfr1 axis.IUBMB Life. 2020 Mar;72(3):373-383. doi: 10.1002/iub.2187. Epub 2019 Oct 17. IUBMB Life. 2020. PMID: 31622017
-
Cardiac innervation in acute myocardial ischaemia/reperfusion injury and cardioprotection.Cardiovasc Res. 2019 Jun 1;115(7):1167-1177. doi: 10.1093/cvr/cvz053. Cardiovasc Res. 2019. PMID: 30796814 Free PMC article. Review.
-
Mitochondria in acute myocardial infarction and cardioprotection.EBioMedicine. 2020 Jul;57:102884. doi: 10.1016/j.ebiom.2020.102884. Epub 2020 Jul 10. EBioMedicine. 2020. PMID: 32653860 Free PMC article. Review.
-
Regulatory non-coding RNAs in acute myocardial infarction.J Cell Mol Med. 2017 May;21(5):1013-1023. doi: 10.1111/jcmm.13032. Epub 2016 Nov 23. J Cell Mol Med. 2017. PMID: 27878945 Free PMC article. Review.
Cited by
-
Putative therapeutic impacts of cardiac CTRP9 in ischaemia/reperfusion injury.J Cell Mol Med. 2022 Jun;26(11):3120-3132. doi: 10.1111/jcmm.17355. Epub 2022 May 10. J Cell Mol Med. 2022. PMID: 35535510 Free PMC article. Review.
-
Novel Roles of Non-Coding RNAs in Opioid Signaling and Cardioprotection.Noncoding RNA. 2018 Sep 17;4(3):22. doi: 10.3390/ncrna4030022. Noncoding RNA. 2018. PMID: 30227648 Free PMC article. Review.
-
Time-regulated transcripts with the potential to modulate human pluripotent stem cell-derived cardiomyocyte differentiation.Stem Cell Res Ther. 2022 Sep 2;13(1):437. doi: 10.1186/s13287-022-03138-x. Stem Cell Res Ther. 2022. PMID: 36056380 Free PMC article.
-
Deduction of novel genes potentially involved in hypoxic AC16 human cardiomyocytes using next-generation sequencing and bioinformatics approaches.Int J Mol Med. 2018 Nov;42(5):2489-2502. doi: 10.3892/ijmm.2018.3851. Epub 2018 Aug 31. Int J Mol Med. 2018. PMID: 30226555 Free PMC article.
-
LncRNA HOTTIP Knockdown Attenuates Acute Myocardial Infarction via Regulating miR-92a-2/c-Met Axis.Cardiovasc Toxicol. 2022 Apr;22(4):352-364. doi: 10.1007/s12012-021-09717-3. Epub 2022 Jan 19. Cardiovasc Toxicol. 2022. PMID: 35044621 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical