Drug repositioning: a machine-learning approach through data integration
Open accessAbstract
Existing computational methods for drug repositioning either rely only on the gene expression response of cell lines after treatment, or on drug-to-disease relationships, merging several information levels. However, the noisy nature of the gene expression and the scarcity of genomic data for many diseases are important limitations to such approaches. Here we focused on a drug-centered approach by predicting the therapeutic class of FDA-approved compounds, not considering data concerning the diseases. We propose a novel computational approach to predict drug repositioning based on state-of-the-art machine-learning algorithms. We have integrated multiple layers of information: i) on the distances of the drugs based on how similar are their chemical structures, ii) on how close are their targets within the protein-protein interaction network, and iii) on how correlated are the gene expression patterns after treatment. Our classifier reaches high accuracy levels (78%), allowing us to re-interpret the top misclassifications as re-classifications, after rigorous statistical evaluation. Efficient drug repurposing has the potential to significantly impact the whole field of drug development. The results presented here can significantly accelerate the translation into the clinics of known compounds for novel therapeutic uses.
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Machine learning can learn from almost any data type, such as research papers, patient records, images, genes, symptoms, diseases, proteins, tissues, species and drug candidates or compounds that have been shown to affect any of the preceding.
“Machine learning can learn from almost any data type, such as that from research papers, patient records, images, genes, symptoms, diseases, proteins, tissues, species and drug candidates or compounds that have been shown to affect any of the preceding74.”
From Exploiting machine learning for end-to-end drug discovery and development (2019) · cites this paper as [74]
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References 44 · Cited by 349
- Authors
- Napolitano, F., Zhao, Y., Moreira, V. M., Tagliaferri, R., Kere, J., D’Amato, M., & Greco, D.
- Affiliations
- University of Salerno (IT)
- University of Helsinki (FI)
- Karolinska Institutet (SE)
- Corresponding author
- Greco, Dario
- ORCID
- Venue
- Journal of Cheminformatics
- Published
- 2013-06-22
- Volume
- 5
- Issue
- 1
- Pages
- 30-30
- ISSN
- 1758-2946 (ISSN-L)
- PMC
- PMC3704944
- OpenAlex
- W2100929382
- Cited by
- 349
- References
- 44
- Citations by year
- 2026: 12 · 2025: 27 · 2024: 35 · 2023: 30 · 2022: 42 · 2021: 25 · 2020: 46 · 2019: 43 · 2018: 26 · 2017: 19 · 2016: 17 · 2015: 14 · 2014: 10 · 2013: 2
- FWCI
- 16.06
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Journal of Cheminformatics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Strathprints: The University of Strathclyde institutional repository (University of Strathclyde) (acceptedVersion, cc-by)
- Funders
- European Commission (228398)
- Academy of Finland
- Suomen Kulttuurirahasto
- Ella ja Georg Ehrnroothin Säätiö
- Magnus Ehrnroothin Säätiö
- Novo Nordisk
- Vetenskapsrådet
- Topics
- Physical Sciences › Computer Science › Computational Theory and Mathematics › Computational Drug Discovery Methods
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biomedical Text Mining and Ontologies
- Keywords
- drug repurposing, machine learning classification, molecular similarity, protein-protein interaction network, gene expression response, drug-target interactions, FDA-approved drugs, data integration
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