NeuTox 2.0: A hybrid deep learning architecture for screening potential neurotoxicity of chemicals based on multimodal feature fusion

Chemically induced neurotoxicity is a critical aspect of chemical safety assessment. Traditional and costly experimental methods call for the development of high-throughput virtual screening. However, the small datasets of neurotoxicity have limited the application of advanced deep learning techniques. The current study developed a hybrid deep learning architecture, NeuTox 2.0, through multimodal feature fusion for enhanced prediction accuracy and generalization ability. We incorporated transfer learning based on self-supervised learning, graph neural networks, and molecular fingerprints/descriptors. Four datasets were used to profile neurotoxicity; these were related to blood-brain barrier permeability, neuronal cytotoxicity, microelectrode array-based neural activity, and mammalian neurotoxicity. Comprehensive performance evaluations demonstrated that NeuTox 2.0 has relatively higher predictive capability across all statistical metrics. Specifically, NeuTox 2.0 exhibits remarkable performance in three of the four datasets. In the BBB dataset, although it does not outperform the PaDEL descriptor model, its performance closely approximates that of the top single-modal model. The ablation experiments indicated that NeuTox 2.0 can learn the deeper structural differences of molecules from various feature extractions and capture complex interactions and mapping relationships between various modalities, thereby improving performance for neurotoxicity prediction. Evaluations of anti-noise ability indicated that NeuTox 2.0 has excellent noise resistance relative to traditional machine learning. We applied the NeuTox 2.0 model to predict the neurotoxicity of 315,790 compounds in the REACH database. The results showed that 701 compounds exhibited potential neurotoxicity in the four neurotoxicity-related predictions. In conclusion, NeuTox 2.0 can be used as an efficient tool for early neurotoxicity screening of environmental chemicals.

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Publication Details

Journal
Environment International
Published
2024-12-28
DOI
https://doi.org/10.1016/j.envint.2024.109244
Citations
12
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
4.34

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article

NeuTox 2.0: A hybrid deep learning architecture for screening potential neurotoxicity of chemicals based on multimodal feature fusion

Huiming Cao, Ling Wang, Yong Liang, Xuejun He et al.
12 citations
Environment International
Computational Drug Discovery Methods
4.34
article

NeuTox 2.0: A hybrid deep learning architecture for screening potential neurotoxicity of chemicals based on multimodal feature fusion

Huiming Cao, Ling Wang, Yong Liang, Xuejun He, Ying Yang, Yuzhen Sun, Xudi Pang
article en
12 citations

Abstract

Chemically induced neurotoxicity is a critical aspect of chemical safety assessment. Traditional and costly experimental methods call for the development of high-throughput virtual screening. However, the small datasets of neurotoxicity have limited the application of advanced deep learning techniques. The current study developed a hybrid deep learning architecture, NeuTox 2.0, through multimodal feature fusion for enhanced prediction accuracy and generalization ability. We incorporated transfer learning based on self-supervised learning, graph neural networks, and molecular fingerprints/descriptors. Four datasets were used to profile neurotoxicity; these were related to blood-brain barrier permeability, neuronal cytotoxicity, microelectrode array-based neural activity, and mammalian neurotoxicity. Comprehensive performance evaluations demonstrated that NeuTox 2.0 has relatively higher predictive capability across all statistical metrics. Specifically, NeuTox 2.0 exhibits remarkable performance in three of the four datasets. In the BBB dataset, although it does not outperform the PaDEL descriptor model, its performance closely approximates that of the top single-modal model. The ablation experiments indicated that NeuTox 2.0 can learn the deeper structural differences of molecules from various feature extractions and capture complex interactions and mapping relationships between various modalities, thereby improving performance for neurotoxicity prediction. Evaluations of anti-noise ability indicated that NeuTox 2.0 has excellent noise resistance relative to traditional machine learning. We applied the NeuTox 2.0 model to predict the neurotoxicity of 315,790 compounds in the REACH database. The results showed that 701 compounds exhibited potential neurotoxicity in the four neurotoxicity-related predictions. In conclusion, NeuTox 2.0 can be used as an efficient tool for early neurotoxicity screening of environmental chemicals.

Environment InternationalVol. 195
Jianghan University (CN)
National Natural Science Foundation of China, Jianghan University, National Key Research and Development Program of China
Openalex Percentile: Top 5%
Computational Drug Discovery Methods
4.34
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