Combination therapies represent one of the most effective strategy in inducing cancer cell death and reducing the risk to develop drug resistance. The identification of putative novel drug combinations, which typically requires the execution of expensive and time consuming lab experiments, can be supported by the synergistic use of mathematical models and multi-objective optimization algorithms. The computational approach allows to automatically search for potential therapeutic combinations and to test their effectiveness in silico, thus reducing the costs of time and money, and driving the experiments toward the most promising therapies. In this work, we couple dynamic fuzzy modeling of cancer cells with different multi-objective optimization algorithm, and we compare their performance in identifying drug target combinations. Specifically, we perform batches of optimizations with 3 and 4 objective functions defined to achieve a desired behavior of the system (e.g., maximize apoptosis while minimizing necrosis and survival), and we compare the quality of the solutions included in the Pareto fronts. Our results show that both the choice of the multi-objective algorithm and the formulation of the optimization problem have an impact on the identified solutions, highlighting the strengths as well as the limitations of this approach.

Spolaor, S., Papetti, D., Cazzaniga, P., Besozzi, D., Nobile, M. (2021). A comparison of multi-objective optimization algorithms to identify drug target combinations. In 2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology, CIBCB 2021 (pp.1-8) [10.1109/CIBCB49929.2021.9562773].

A comparison of multi-objective optimization algorithms to identify drug target combinations

Spolaor S.;Papetti D. M.;Besozzi D.;Nobile M. S.
2021

Abstract

Combination therapies represent one of the most effective strategy in inducing cancer cell death and reducing the risk to develop drug resistance. The identification of putative novel drug combinations, which typically requires the execution of expensive and time consuming lab experiments, can be supported by the synergistic use of mathematical models and multi-objective optimization algorithms. The computational approach allows to automatically search for potential therapeutic combinations and to test their effectiveness in silico, thus reducing the costs of time and money, and driving the experiments toward the most promising therapies. In this work, we couple dynamic fuzzy modeling of cancer cells with different multi-objective optimization algorithm, and we compare their performance in identifying drug target combinations. Specifically, we perform batches of optimizations with 3 and 4 objective functions defined to achieve a desired behavior of the system (e.g., maximize apoptosis while minimizing necrosis and survival), and we compare the quality of the solutions included in the Pareto fronts. Our results show that both the choice of the multi-objective algorithm and the formulation of the optimization problem have an impact on the identified solutions, highlighting the strengths as well as the limitations of this approach.
slide + paper
Cancer; Combination chemotherapy; Fuzzy modeling; Global optimization; Multi-objective optimization; Therapeutic targets;
English
2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology, CIBCB 2021 - 13 October 2021 through 15 October 2021
2021
Hallinan, J; Chetty, M; Heredia, GR; Shatte, A; Lim, S
2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology, CIBCB 2021
978-1-6654-0112-8
2021
1
8
none
Spolaor, S., Papetti, D., Cazzaniga, P., Besozzi, D., Nobile, M. (2021). A comparison of multi-objective optimization algorithms to identify drug target combinations. In 2021 IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology, CIBCB 2021 (pp.1-8) [10.1109/CIBCB49929.2021.9562773].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/391250
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