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Updated: May 12, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
Published on: October 7, 2025
microRNAs as pharmacological targets in cancer
Aroa Soriano1, Luz Jubierre, Ana Almazán-Moga
1Laboratory of Translational Research in Childhood Cancer, Vall d'Hebron Institut de Recerca, Universitat Autónoma de Barcelona, Spain.
Abstract:
The survival rate of cancer patients has increased considerably in the last 20 years owing to significant efforts made in prevention, early detection protocols, combined chemotherapy regimens, targeted therapies, refined radiotherapy and cancer vaccines. However, metastasis and acquired resistance to current therapies represent two major challenges for achieving long-term cure. Therefore, new treatment strategies must be developed. One promising alternative is epigenetic-based therapies, of which miRNAs are at the forefront. MicroRNAs are endogenous small non-coding RNAs, often deregulated in cancer, which regulate gene expression by specific binding to the 3'-UTR of target genes. They are excellent candidates for therapy since miRNAs can regulate multiple targets of the same or different pathways, thereby minimizing the risk of resistance development or compensatory mechanisms. In this review, the mechanisms that lead to miRNA deregulation in cancer, their feasibility as therapeutic tools and the different strategies for the pharmacological manipulation of miRNAs in preclinical animal models are discussed.
Insights
MicroRNAs (miRNAs) offer a promising new avenue for cancer treatment by targeting multiple genes simultaneously. This approach aims to overcome challenges like metastasis and therapy resistance, improving patient survival rates.
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- Cancer patient survival has improved due to advances in prevention, early detection, and therapies.
- Metastasis and acquired resistance to existing treatments remain significant hurdles for long-term cancer cure.
- Novel therapeutic strategies are essential to address these persistent challenges in cancer treatment.
Purpose of the Study:
- To review the mechanisms of microRNA (miRNA) deregulation in cancer.
- To assess the therapeutic potential of miRNAs as a novel cancer treatment strategy.
- To discuss various approaches for the pharmacological manipulation of miRNAs in preclinical cancer models.
Main Methods:
- Literature review of epigenetic-based therapies, focusing on miRNAs.
- Analysis of miRNA biogenesis and function in cancer gene regulation.
- Examination of preclinical studies involving miRNA-targeted cancer therapies.
Main Results:
- MicroRNAs are small non-coding RNAs that regulate gene expression and are frequently deregulated in cancer.
- miRNAs can target multiple genes within the same or different pathways, potentially reducing treatment resistance.
- Pharmacological strategies for miRNA manipulation show promise in preclinical cancer models.
Conclusions:
- Epigenetic therapies, particularly those involving miRNAs, represent a promising frontier in cancer treatment.
- The ability of miRNAs to regulate multiple targets offers a potential advantage over conventional therapies in overcoming resistance.
- Further research and development of miRNA-based therapeutics are warranted for improved cancer patient outcomes.
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