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Updated: Feb 16, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Development of Novel Therapeutic Agents by Inhibition of Oncogenic MicroRNAs
Dinh-Duc Nguyen1, Suhwan Chang2
1Department of Biomedical Sciences, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea. michaelnguyen1986@gmail.com.
Abstract:
MicroRNAs (miRs, miRNAs) are regulatory small noncoding RNAs, with their roles already confirmed to be important for post-transcriptional regulation of gene expression affecting cell physiology and disease development. Upregulation of a cancer-causing miRNA, known as oncogenic miRNA, has been found in many types of cancers and, therefore, represents a potential new class of targets for therapeutic inhibition. Several strategies have been developed in recent years to inhibit oncogenic miRNAs. Among them is a direct approach that targets mature oncogenic miRNA with an antisense sequence known as antimiR, which could be an oligonucleotide or miRNA sponge. In contrast, an indirect approach is to block the biogenesis of miRNA by genome editing using the CRISPR/Cas9 system or a small molecule inhibitor. The development of these inhibitors is straightforward but involves significant scientific and therapeutic challenges that need to be resolved. In this review, we summarize recent relevant studies on the development of miRNA inhibitors against cancer.
Insights
This review covers microRNA (miRNA) inhibitors for cancer therapy. Strategies include direct antimiR targeting and indirect inhibition of miRNA biogenesis, addressing key challenges in cancer treatment.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- MicroRNAs (miRNAs) are small noncoding RNAs regulating gene expression.
- Oncogenic miRNAs are upregulated in cancers, presenting therapeutic targets.
Purpose of the Study:
- To review recent developments in miRNA inhibitors for cancer therapy.
- To summarize strategies for inhibiting oncogenic miRNAs.
Main Methods:
- Direct inhibition using antisense oligonucleotides (antimiRs) or miRNA sponges.
- Indirect inhibition via genome editing (CRISPR/Cas9) or small molecule inhibitors to block miRNA biogenesis.
Main Results:
- Various strategies have been developed to inhibit oncogenic miRNAs.
- Both direct and indirect approaches face scientific and therapeutic challenges.
Conclusions:
- miRNA inhibitors offer a promising new class of cancer therapeutics.
- Further research is needed to overcome challenges in developing effective miRNA inhibitors.
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