Tiny Guides, Big Impact: Focus on the Opportunities and Challenges of miR-Based Treatments for ARDS
- PMID: 38474059
- PMCID: PMC10931977
- DOI: 10.3390/ijms25052812
Tiny Guides, Big Impact: Focus on the Opportunities and Challenges of miR-Based Treatments for ARDS
Abstract
Acute Respiratory Distress Syndrome (ARDS) is characterized by lung inflammation and increased membrane permeability, which represents the leading cause of mortality in ICUs. Mechanical ventilation strategies are at the forefront of supportive approaches for ARDS. Recently, an increasing understanding of RNA biology, function, and regulation, as well as the success of RNA vaccines, has spurred enthusiasm for the emergence of novel RNA-based therapeutics. The most common types of RNA seen in development are silencing (si)RNAs, antisense oligonucleotide therapy (ASO), and messenger (m)RNAs that collectively account for 80% of the RNA therapeutics pipeline. These three RNA platforms are the most mature, with approved products and demonstrated commercial success. Most recently, miRNAs have emerged as pivotal regulators of gene expression. Their dysregulation in various clinical conditions offers insights into ARDS pathogenesis and offers the innovative possibility of using microRNAs as targeted therapy. This review synthesizes the current state of the literature to contextualize the therapeutic potential of miRNA modulation. It considers the potential for miR-based therapeutics as a nuanced approach that incorporates the complexity of ARDS pathophysiology and the multifaceted nature of miRNA interactions.
Keywords: ARDS; gene therapy; miRNA; nanotechnology.
Conflict of interest statement
The authors declare no conflicts of interest.
Similar articles
-
MicroRNA and mRNA expression profiling in rat acute respiratory distress syndrome.BMC Med Genomics. 2014 Jul 28;7:46. doi: 10.1186/1755-8794-7-46. BMC Med Genomics. 2014. PMID: 25070658 Free PMC article.
-
The Role of MicroRNAs in Acute Respiratory Distress Syndrome and Sepsis, From Targets to Therapies: A Narrative Review.Anesth Analg. 2020 Nov;131(5):1471-1484. doi: 10.1213/ANE.0000000000005146. Anesth Analg. 2020. PMID: 33079870 Free PMC article. Review.
-
Targeting MALAT1 and miRNA-181a-5p for the intervention of acute lung injury/acute respiratory distress syndrome.Respir Med. 2020 Dec;175:106210. doi: 10.1016/j.rmed.2020.106210. Epub 2020 Nov 4. Respir Med. 2020. Retraction in: Respir Med. 2021 Nov;188:106601. doi: 10.1016/j.rmed.2021.106601. PMID: 33197806 Free PMC article. Retracted.
-
Circulating miRNA 887 is differentially expressed in ARDS and modulates endothelial function.Am J Physiol Lung Cell Mol Physiol. 2020 Jun 1;318(6):L1261-L1269. doi: 10.1152/ajplung.00494.2019. Epub 2020 Apr 22. Am J Physiol Lung Cell Mol Physiol. 2020. PMID: 32321279 Free PMC article.
-
Delivery systems of therapeutic nucleic acids for the treatment of acute lung injury/acute respiratory distress syndrome.J Control Release. 2023 Aug;360:1-14. doi: 10.1016/j.jconrel.2023.06.018. Epub 2023 Jun 19. J Control Release. 2023. PMID: 37330013 Review.
References
-
- Mohammed A., Alghetaa H., Sultan M., Singh N.P., Nagarkatti P., Nagarkatti M. Administration of Δ9-Tetrahydrocannabinol (THC) Post-Staphylococcal Enterotoxin B Exposure Protects Mice From Acute Respiratory Distress Syndrome and Toxicity. Front. Pharmacol. 2020;11:893. doi: 10.3389/fphar.2020.00893. - DOI - PMC - PubMed
-
- Alghetaa H., Mohammed A., Singh N., Wilson K., Cai G., Putluri N., Nagarkatti M., Nagarkatti P. Resveratrol attenuates staphylococcal enterotoxin B-activated immune cell metabolism via upregulation of miR-100 and suppression of mTOR signaling pathway. Front. Pharmacol. 2023;14:1106733. doi: 10.3389/fphar.2023.1106733. - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical