Exploring AI-Driven Drug Repurposing Strategies Targeting ErbB Signalling Pathway for Brain Cancer Therapy

This study explores the application of machine learning methodologies in drug repurposing for brain cancer therapy, focusing on targeting the epidermal growth factor receptor (EGFR). Our approach involved the development of a predictive model to estimate the half-maximal inhibitory concentration (IC50) values of compounds against EGFR, leveraging existing biological activity data of known EGFR inhibitors and molecular structure descriptors. The constructed model exhibited efficacy in predicting the inhibitory activity of compounds against EGFR. Subsequent screening of a library of known drugs using the predictive model led to the identification of several compounds with low predicted IC50 values, indicating their potential as drug candidates for further investigation. This study underscores the utility of integrating machine learning techniques into drug repurposing endeavours, offering a pragmatic approach to identifying potential therapeutic options for brain cancer treatment.

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Publication Details

Published
2024-08-08
DOI
https://doi.org/10.1109/cis-ram61939.2024.10673264
Citations
1
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.36
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article

Exploring AI-Driven Drug Repurposing Strategies Targeting ErbB Signalling Pathway for Brain Cancer Therapy

Mingming Quan, Jianqiao Long, Jichun Li, Chi Kit Ng et al.
1 citations
Computational Drug Discovery Methods
0.36
article

Exploring AI-Driven Drug Repurposing Strategies Targeting ErbB Signalling Pathway for Brain Cancer Therapy

Mingming Quan, Jianqiao Long, Jichun Li, Chi Kit Ng, Muran Tang
article en
1 citations

Abstract

This study explores the application of machine learning methodologies in drug repurposing for brain cancer therapy, focusing on targeting the epidermal growth factor receptor (EGFR). Our approach involved the development of a predictive model to estimate the half-maximal inhibitory concentration (IC50) values of compounds against EGFR, leveraging existing biological activity data of known EGFR inhibitors and molecular structure descriptors. The constructed model exhibited efficacy in predicting the inhibitory activity of compounds against EGFR. Subsequent screening of a library of known drugs using the predictive model led to the identification of several compounds with low predicted IC50 values, indicating their potential as drug candidates for further investigation. This study underscores the utility of integrating machine learning techniques into drug repurposing endeavours, offering a pragmatic approach to identifying potential therapeutic options for brain cancer treatment.

Vol. 1
Newcastle University (GB)
Good health and well-being
Openalex Percentile: Top 36%
Computational Drug Discovery Methods
0.36
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