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Journal article : Review

Small molecule-mediated targeting of microRNAs for drug discovery: experiments, computational techniques, and disease implications

Abstract:
Small molecules have been providing medical breakthroughs for human diseases for more than a century. Recently, identifying small molecule inhibitors that target microRNAs (miRNAs) has gained importance, despite the challenges posed by labour-intensive screening experiments and the significant efforts required for medicinal chemistry optimization. Numerous experimentally-verified cases have demonstrated the potential of miRNA-targeted small molecule inhibitors for disease treatment. This new approach is grounded in their posttranscriptional regulation of the expression of disease-associated genes. Reversing dysregulated gene expression using this mechanism may help control dysfunctional pathways. Furthermore, the ongoing improvement of algorithms has allowed for the integration of computational strategies built on top of laboratory-based data, facilitating a more precise and rational design and discovery of lead compounds. To complement the use of extensive pharmacogenomics data in prioritising potential drugs, our previous work introduced a computational approach based on only molecular sequences. Moreover, various computational tools for predicting molecular interactions in biological networks using similarity-based inference techniques have been accumulated in established studies. However, there are a limited number of comprehensive reviews covering both computational and experimental drug discovery processes. In this review, we outline a cohesive overview of both biological and computational applications in miRNA-targeted drug discovery, along with their disease implications and clinical significance. Finally, utilizing drug-target interaction (DTIs) data from DrugBank, we showcase the effectiveness of deep learning for obtaining the physicochemical characterization of DTIs.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.ejmech.2023.115500

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Botnar Research Centre
Role:
Author
ORCID:
0000-0002-1274-5080
More by this author
Role:
Author
ORCID:
0000-0002-6757-6018
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Sub department:
Botnar Research Centre
Role:
Author


Publisher:
Elsevier
Journal:
European Journal of Medicinal Chemistry More from this journal
Volume:
257
Article number:
115500
Place of publication:
France
Publication date:
2023-05-17
Acceptance date:
2023-05-15
DOI:
ISSN:
0223-5234
Pmid:
37262996


Language:
English
Keywords:
Subtype:
Review
Pubs id:
1350164
Local pid:
pubs:1350164
Deposit date:
2023-08-01
ARK identifier:

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