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  2. MT-EpiPred: Multitask Learning for Prediction of Small-Molecule Epigenetic Modulators

MT-EpiPred: Multitask Learning for Prediction of Small-Molecule Epigenetic Modulators

  • J Chem Inf Model. 2023 Dec 18. doi: 10.1021/acs.jcim.3c01368.
Ruihan Zhang 1 Xingran Xie 1 Dongxuan Ni 1 Hairong Wang 1 Jin Li 1 Weilie Xiao 1
Affiliations

Affiliation

  • 1 Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education; Yunnan Key Laboratory of Research and Development for Natural Products; The Cloud Computing Engineering Research Center of Yunnan Province; Key Laboratory of Software Engineering of Yunnan Province; School of Software; School of Pharmacy, Yunnan University, Kunming 650500, P. R. China.
Abstract

Epigenetic modulators play an increasingly crucial role in the treatment of various diseases. In this case, it is imperative to systematically investigate the activity of these agents and understand their influence on the entire epigenetic regulatory network rather than solely concentrate on individual targets. This work introduces MT-EpiPred, a multitask learning method capable of predicting the activity of compounds against 78 epigenetic targets. MT-EpiPred demonstrated outstanding performance, boasting an average auROC of 0.915 and the ability to handle few-shot targets. In comparison to the existing method, MT-EpiPred not only expands the target pool but also achieves superior predictive performance with the same data set. MT-EpiPred was then applied to predict the epigenetic target of a newly synthesized compound (1), where the molecular target was unknown. The method identified KDM4D as a potential target, which was subsequently validated through an in vitro Enzyme inhibition assay, revealing an IC50 of 4.8 μM. The MT-EpiPred method has been implemented in the web server MT-EpiPred (http://epipred.com), providing free accessibility. In summary, this work presents a convenient and accurate tool for discovering novel small-molecule epigenetic modulators, particularly in the development of selective inhibitors and evaluating the impact of these inhibitors over a broad epigenetic network.

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