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. 2022 Nov 30;23(23):15013. doi: 10.3390/ijms232315013

Table 1.

A list of research studies evaluating out the role of microRNA that play a role in oxidative-stress mechanisms involved in heart failure according to the sections.

No. miRNA Ref. Type of Study 1 Techniqe 2 Main Conclusion
3.1 Mitochondrial integrity and function
1 miRNA-690 Wang, X. et al. (2017) [24] animal RT qRT-PCR microRNAs were enriched in mitochondria during heart failure, which establishes a link between microRNA and mitochondrion in heart failure.
miRNA-696
miRNA-532-5p
miRNA-345-3p
2 miRNA-122 Shi, Y. et al. (2021) [25] animal qRT-PCR with the miRCute Enhanced Fluorescence Quantitative Assay Kit (Tiangen) miR-122 causes cardiomyocyte apoptosis by inhibiting Hand2 transcription factor and consequently increasing mitochondrial fission. This mechanism likely contributes to heart failure and modulating this pathway could be therapeutically valuable against heart failure.
3 miRNA-15b Roy, S. et al. (2013) [26] animal/in vivo qRT-PCR Suppression of inducible miRNA-15b can prevent rapid loss of cardiac function in an animal adult heart and can be a key approach worthy of therapeutic consideration.
3.2 Antioxidant defence
4 miRNA-27a Tian, C. et al. (2018) [27] animal/in vivo qRT-PCR Increased expression of local microRNAs induced by myocardial infarction may contribute to oxidative stress by the inhibition of nuclear factor erythroid 2-related factor 2(NRF2) translation in chronic heart failure.
miRNA-28-3p
miRNA-34a
5 miRNA-27a * Tian, C. et al. (2020) [28] animal/in vivo qRT-PCR Cardiac fibroblast-secretion of miRNA27a *-enriched extracellular vesicles (EV) might act as a paracrine signaling mediator of cardiac hypertrophy and may have a potential to become novel therapeutic target.
6 miRNA-24-3p Shimizu, T. et al. (2020) [29] animal RNA-sequencing, western blot, ELISA Protein kinase R–like endoplasmic reticulum (ER) kinase (PERK)-mediated suppression of miRNAs by sildenafil improves cardiac dysfunction in heart failure.
3.3 Iron overload and ferroptosis
7 miRNA-224-5p Zheng, H. et al. (2021) [30] animal qRT-PCR, Western blot analysis, luciferase reporter assay Circulatory RNA (circRNA), microRNA(miRNA) and mRNA work in a regulatory network and reveal potential targets for the treatment of heart failure.
miRNA-296-3p
miRNA-671-5p
miRNA-1306-5p
miRNA-3082-5p
3.4 Cardiac hypertrophy and remodelling
8 miRNA-21-3p Zhao, Y. et al. (2018) [31] animal miRNA microarray, bioinforma-tic analysis, qRT-PCR, Western blot The injection of Yiqifumai (YQFM) has a potential effect which alleviates cardiac hypertrophy and apoptosis in chronic heart failure by miRNA expression regulation.
miRNA216-5p
miRNA-219a-2-3p
miRNA-381-3p
miRNA-466c-5p
miRNA-542-3p
miRNA-702-5p
9 miRNA-93 Su, Q. et al. (2019) [32] animal/in vivo RT qRT-PCR, ELISA, Western blot Upregulated miR-93 and downregulated LIM domain kinase 1 (LIMK1) reduce cardiac dysfunction and improve ventricular remodelling in rats with chronic heart failure.
10 miRNA-142-5p Sharma, S. et al. (2012) [33] animal/in vivo qRT-PCR, Western blot Downregulation of miR-142 is a critical element of adaptive cardiac muscle hypertrophy in response to hemodynamic stress.
miRNA-142-3p
11 miRNA-195-5p Shen, Y. et al. (2020) [34] animal RT qRT-PCR Depleting miR-195-5p and up-regulating Chemokine receptor type 4 alleviates cardiac function injury in mice with heart failure and may be a potential candidate marker and therapeutic target for heart failure.
For Section 3.4 see also research studies no.: 4 [27] and 5 [28].
3.5 Apoptosis
12 miRNA-454 Wang, Y. et al. (2021) [35] animal RT qRT-PCR, Western blot The cardioprotective role of miR-454 is achieved through activation of the cyclic adenosine 3′5′-monophosphate(cAMP).
3.6 Human studies
13 miRNA-129-5p Ramachandran, S. et al. (2017) [36] human isolation of mir129-5p from plasma microvesicles, qRT-PCR miR129-5p was found to be a sensitive and specific biomarker for heart failure in univentricular heart disease in pediatric patients independent of ventricular morphology or stage of palliation.
14 miRNA-208a Mohammadi et al. (2021) [37] human qRT-PCR The results on different populations of cardiovascular patients (after myocardial infarction, with arrhythmia, heart failure etc.) showed increases in both oxidative stress, inflammation, apoptotic factors, and in the expression of miR-208a.
3.7 Therapeutic potential
15 miRNA-15b Roy, S. et al. (2013) [26] animal/in vivo qRT-PCR Suppression of inducible miRNA-15b can prevent rapid loss of cardiac function in an animal adult heart and can be a key approach worthy of therapeutic consideration.
For Section 3.5 see also research studies no.: 5 [28] and 11 [34].

1 Types of study include: review, human—study based on human participants, animal—study based on animal models, in vivo—study based on research inside the organism. 2 qRT-PCR—quantitative Real-Time Polymerase Chain Reaction, RT qRT-PCR—Reverse Transcriptase quantitative Real-Time Polymerase Chain Reaction, *—passenger strand.