Publication: Origin of aromatase inhibitory activity via proteochemometric modeling
2
Issued Date
2016-01-01
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ISSN
21678359
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2-s2.0-84971524531
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Mahidol University
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SCOPUS
Bibliographic Citation
PeerJ. Vol.2016, No.5 (2016)
Suggested Citation
Saw Simeon, Ola Spjuth, Maris Lapins, Sunanta Nabu, Nuttapat Anuwongcharoen, Virapong Prachayasittikul, Jarl E.S. Wikberg, Chanin Nantasenamat Origin of aromatase inhibitory activity via proteochemometric modeling. PeerJ. Vol.2016, No.5 (2016). doi:10.7717/peerj.1979 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/42137
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Title
Origin of aromatase inhibitory activity via proteochemometric modeling
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Abstract
© 2016 Simeon et al. Aromatase, the rate-limiting enzyme that catalyzes the conversion of androgen to estrogen, plays an essential role in the development of estrogen-dependent breast cancer. Side effects due to aromatase inhibitors (AIs) necessitate the pursuit of novel inhibitor candidates with high selectivity, lower toxicity and increased potency. Designing a novel therapeutic agent against aromatase could be achieved computationally by means of ligand-based and structure-based methods. For over a decade, we have utilized both approaches to design potential AIs for which quantitative structure-activity relationships and molecular docking were used to explore inhibitory mechanisms of AIs towards aromatase. However, such approaches do not consider the effects that aromatase variants have on different AIs. In this study, proteochemometrics modeling was applied to analyze the interaction space between AIs and aromatase variants as a function of their substructural and amino acid features. Good predictive performance was achieved, as rigorously verified by 10-fold cross-validation, external validation, leave-one-compound-out cross-validation, leave-one-protein-out cross-validation and Y-scrambling tests. The investigations presented herein provide important insights into the mechanisms of aromatase inhibitory activity that could aid in the design of novel potent AIs as breast cancer therapeutic agents.