Related Experiment Video
Updated: May 24, 2026

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as a Novel Detection and Quantification Method
Published on: October 7, 2025
Identification of links between small molecules and miRNAs in human cancers based on transcriptional responses
Wei Jiang1, Xiaowen Chen, Mingzhi Liao
1College of Bioinformatics Science and Technology and State-Province Key Laboratories of Biomedicine-Pharmaceutics of China, Harbin Medical University, Harbin, Heilongjiang 150081, PR China.
Abstract:
The use of small molecules to target miRNAs is a new type of therapy for human diseases, particularly cancers. We proposed a novel high-throughput approach to identify the biological links between small molecules and miRNAs in 23 different cancers and constructed the Small Molecule-MiRNA Network (SMirN) for each cancer to systematically analyze the properties of their associations. In each SMirN, we partitioned small molecules (miRNAs) into modules, in which small molecules (miRNAs) were connected with one miRNA (small molecule). Almost all of the miRNA modules comprised miRNAs that had similar target genes and functions or were members of the same miRNA family. Most of the small molecule modules involved compounds with similar chemical structures, modes of action, or drug interactions. These modules can be used to identify drug candidates and new indications for existing drugs. Therefore, our approach is valuable to drug discovery and cancer therapy.
Insights
This study introduces a new method to link small molecules with microRNAs (miRNAs) across 23 cancers. The developed Small Molecule-MiRNA Network (SMirN) aids in discovering new cancer drug candidates and therapies.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Targeting microRNAs (miRNAs) with small molecules represents a novel therapeutic strategy for human diseases, especially cancers.
- Understanding the complex interactions between small molecules and miRNAs is crucial for developing effective cancer treatments.
Purpose of the Study:
- To develop a high-throughput approach for identifying biological links between small molecules and miRNAs in 23 distinct cancer types.
- To construct and analyze Small Molecule-MiRNA Networks (SMirNs) for systematic characterization of these associations.
Main Methods:
- A novel high-throughput screening method was employed to identify interactions.
- Small Molecule-MiRNA Networks (SMirNs) were constructed for 23 cancer types.
- Network analysis involved partitioning molecules and miRNAs into functional modules based on connectivity.
Main Results:
- MiRNA modules predominantly contained miRNAs with similar target genes, functions, or family memberships.
- Small molecule modules typically comprised compounds with shared chemical structures, modes of action, or drug interactions.
- The identified modules facilitate the discovery of potential drug candidates and repurposing opportunities for existing drugs.
Conclusions:
- The developed approach provides a systematic framework for analyzing small molecule-miRNA interactions in cancer.
- The constructed SMirNs offer valuable insights for accelerating drug discovery and advancing cancer therapy.
- This methodology holds significant potential for identifying novel therapeutic strategies in oncology.
Related Concept Videos
MicroRNAs
MicroRNAs
MicroRNAs
lncRNA - Long Non-coding RNAs

