A network-driven computational framework for identifying FDA-approved drug repurposing across heterogeneous brain cancers

The proposed profile-network-based method achieved 70%-95% accuracy for drug repurposing across different disease categories related to the brain. <i>In-mac</i> and ReBrain were used for the repurposing of known drugs for the treatment of brain cancer. As a result, three repurposed drugs were identified as priorities: (i) mefloquine (reference drug: vorasidenib citrate), (ii) clofibric acid (reference drug: carmustine), and armillarisin A (reference drug: lomustine). These results also suggest repurposing candidates for synergistic combinations across different brain tumors. The two applications developed in this work are freely accessible and in the public domain at https://assay.smallmoles.com/escorwin.

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Publication Details

Journal
Frontiers in Molecular Biosciences
Published
2026-02-17
DOI
https://doi.org/10.3389/fmolb.2026.1768081
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

A network-driven computational framework for identifying FDA-approved drug repurposing across heterogeneous brain cancers

Om Prakash
Frontiers in Molecular Biosciences
Computational Drug Discovery Methods
article

A network-driven computational framework for identifying FDA-approved drug repurposing across heterogeneous brain cancers

Om Prakash
article en

Abstract

The proposed profile-network-based method achieved 70%-95% accuracy for drug repurposing across different disease categories related to the brain. <i>In-mac</i> and ReBrain were used for the repurposing of known drugs for the treatment of brain cancer. As a result, three repurposed drugs were identified as priorities: (i) mefloquine (reference drug: vorasidenib citrate), (ii) clofibric acid (reference drug: carmustine), and armillarisin A (reference drug: lomustine). These results also suggest repurposing candidates for synergistic combinations across different brain tumors. The two applications developed in this work are freely accessible and in the public domain at https://assay.smallmoles.com/escorwin.

Frontiers in Molecular BiosciencesVol. 13
Institute of Mathematical Sciences, Division of Mathematical Sciences
Openalex Percentile: Top 50%
Computational Drug Discovery Methods
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