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Updated: Dec 31, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Therapeutic potential of antagomiRs in haematological and oncological neoplasms
Vanessa Innao1, Alessandro Allegra1, Nicolina Pulvirenti1
1Division of Hematology, Dipartimento di Patologia Umana dell'Adulto e dell'Età Evolutiva "Gaetano Barresi", University of Messina, Messina, Italy.
Background:
The importance of the role of MicroRNAs (or miRNAs) has been emphasised by the large number of studies in human tumour cells, underlining the high impact of post-transcriptional processes in cancer onset, progression, invasion and metastatisation. Currently known as oncomiR, real databases are collecting all the smaller fragments of RNA capable of participating in the oncogenesis.
Aims:
With the aim to collect for the first time the most important acquisitions in literature about antagomiRs in oncology, our narrative review is born with the purpose of showing that specific antisense oligonucleotides, capable to bind and antagonise single or multiple miRNAs, are effective as therapeutic compounds.
Results:
Peptide or locked nucleic acids, miRNA sponges or antagomiRs attached to plasmid or lentiviral vectors carrying miRNA sequences to its target are objects of our analysis, demonstrating their effectiveness in a large number and types of tumours. We have also tried how to overcome their high immunogenicity, which remains its greatest limit for clinical use.
Conclusions:
They are ambitious but fascinating promise to alter the promotion of the tumour growth by binding specific molecular targets, with high precision and low toxicity, leaving the scientists the chance of development as anti-cancer drugs and not just.
Insights
AntagomiRs, which are antisense oligonucleotides targeting microRNAs (miRNAs), show promise as effective cancer therapeutics. These compounds can precisely inhibit oncogenic miRNAs, offering a novel approach to anti-cancer drug development.
Area of Science:
- Oncology
- Molecular Biology
- RNA Therapeutics
Background:
- MicroRNAs (miRNAs) play a crucial role in human cancers by regulating post-transcriptional processes.
- Dysregulated miRNAs, known as oncomiRs, are implicated in cancer initiation, progression, invasion, and metastasis.
- Databases are actively collecting information on small RNA fragments involved in oncogenesis.
Purpose of the Study:
- To review and consolidate key literature findings on antagomiRs in oncology.
- To demonstrate the therapeutic potential of antagomiRs as effective anti-cancer compounds.
- To highlight antagomiRs as specific antisense oligonucleotides that antagonize single or multiple miRNAs.
Main Methods:
- Analysis of various antagomiR delivery systems, including peptide or locked nucleic acids.
- Evaluation of miRNA sponges and antagomiRs conjugated to plasmid or lentiviral vectors.
- Review of strategies to mitigate the high immunogenicity of antagomiRs for clinical application.
Main Results:
- AntagomiRs have demonstrated effectiveness across a wide range of tumor types.
- Various delivery methods, such as peptide conjugates and vector-based systems, show promise.
- Research is actively addressing the challenge of antagomir immunogenicity to facilitate clinical use.
Conclusions:
- AntagomiRs represent a promising therapeutic strategy for cancer treatment.
- These molecules offer precise targeting of molecular pathways involved in tumor growth.
- Further development of antagomiRs could lead to novel anti-cancer drugs with high efficacy and low toxicity.
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