Drug intelligence / Profile preview

miR-21-3p antagomiR

Development stage
Preclinical
Modality
Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Modified DNA Oligonucleotides → Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Single-strand DNA → Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

miR-21-3p antagomiR is a chemically modified antisense oligonucleotide designed to specifically bind to and inhibit the activity of microRNA-21-3p (miR-21-3p), a small non-coding RNA molecule involved in the regulation of gene expression[8]. Inhibition of miR-21-3p has been shown to have protective effects in the heart by altering macrophage polarization (reducing pro-inflammatory M1 phenotype), decreasing excessive mitophagy, and upregulating the mitochondrial fatty acid oxidation enzyme CPT1A, which is crucial for cardiac energy metabolism[1]. This intervention can mitigate myocardial fibrosis, improve cardiac function, and reduce markers of cardiac injury in experimental models of chronic heart failure and sepsis-induced cardiac dysfunction[1]. miR-21-3p antagomiR has also been investigated in other contexts, including wound healing and fibrotic diseases, where modulation of miR-21-3p levels affects fibroblast proliferation and collagen synthesis[3]. While promising in preclinical studies, miR-21-3p antagomiR is not an approved therapy and remains primarily a research tool.

Other names
miR-21-3p inhibitormiR21-3p inhibitormiR 21-3p inhibitorantagomiR-21-3pantagomiR21-3pantagomiR 21-3p
02

Targets

miR-21-3p (microRNA-21-3p)IFNG (Interferon gamma)CPT1A (Carnitine palmitoyltransferase 1A)

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