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      GraphADT: empowering interpretable predictions of acute dermal toxicity with multi-view graph pooling and structure remapping

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      Bioinformatics
      Oxford University Press

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          Abstract

          Motivation

          Accurate prediction of acute dermal toxicity (ADT) is essential for the safe and effective development of contact drugs. Currently, graph neural networks, a form of deep learning technology, accurately model the structure of compound molecules, enhancing predictions of their ADT. However, many existing methods emphasize atom-level information transfer and overlook crucial data conveyed by molecular bonds and their interrelationships. Additionally, these methods often generate “equal” node representations across the entire graph, failing to accentuate “important” substructures like functional groups, pharmacophores, and toxicophores, thereby reducing interpretability.

          Results

          We introduce a novel model, GraphADT, utilizing structure remapping and multi-view graph pooling (MVPool) technologies to accurately predict compound ADT. Initially, our model applies structure remapping to better delineate bonds, transforming “bonds” into new nodes and “bond-atom-bond” interactions into new edges, thereby reconstructing the compound molecular graph. Subsequently, we use MVPool to amalgamate data from various perspectives, minimizing biases inherent to single-view analyses. Following this, the model generates a robust node ranking collaboratively, emphasizing critical nodes or substructures to enhance model interpretability. Lastly, we apply a graph comparison learning strategy to train both the original and structure remapped molecular graphs, deriving the final molecular representation. Experimental results on public datasets indicate that the GraphADT model outperforms existing state-of-the-art models. The GraphADT model has been demonstrated to effectively predict compound ADT, offering potential guidance for the development of contact drugs and related treatments.

          Availability and implementation

          Our code and data are accessible at: https://github.com/mxqmxqmxq/GraphADT.git.

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          Most cited references20

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          A compact review of molecular property prediction with graph neural networks.

          As graph neural networks are becoming more and more powerful and useful in the field of drug discovery, many pharmaceutical companies are getting interested in utilizing these methods for their own in-house frameworks. This is especially compelling for tasks such as the prediction of molecular properties which is often one of the most crucial tasks in computer-aided drug discovery workflows. The immense hype surrounding these kinds of algorithms has led to the development of many different types of promising architectures and in this review we try to structure this highly dynamic field of AI-research by collecting and classifying 80 GNNs that have been used to predict more than 20 molecular properties using 48 different datasets.
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            • Article: found
            Is Open Access

            Machine Learning of Toxicological Big Data Enables Read-Across Structure Activity Relationships (RASAR) Outperforming Animal Test Reproducibility

            Abstract Earlier we created a chemical hazard database via natural language processing of dossiers submitted to the European Chemical Agency with approximately 10 000 chemicals. We identified repeat OECD guideline tests to establish reproducibility of acute oral and dermal toxicity, eye and skin irritation, mutagenicity and skin sensitization. Based on 350–700+ chemicals each, the probability that an OECD guideline animal test would output the same result in a repeat test was 78%–96% (sensitivity 50%–87%). An expanded database with more than 866 000 chemical properties/hazards was used as training data and to model health hazards and chemical properties. The constructed models automate and extend the read-across method of chemical classification. The novel models called RASARs (read-across structure activity relationship) use binary fingerprints and Jaccard distance to define chemical similarity. A large chemical similarity adjacency matrix is constructed from this similarity metric and is used to derive feature vectors for supervised learning. We show results on 9 health hazards from 2 kinds of RASARs—“Simple” and “Data Fusion”. The “Simple” RASAR seeks to duplicate the traditional read-across method, predicting hazard from chemical analogs with known hazard data. The “Data Fusion” RASAR extends this concept by creating large feature vectors from all available property data rather than only the modeled hazard. Simple RASAR models tested in cross-validation achieve 70%–80% balanced accuracies with constraints on tested compounds. Cross validation of data fusion RASARs show balanced accuracies in the 80%–95% range across 9 health hazards with no constraints on tested compounds.
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              Enhanced graph isomorphism network for molecular ADMET properties prediction

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                Author and article information

                Contributors
                Role: MethodologyRole: ValidationRole: Writing - original draft
                Role: MethodologyRole: Supervision
                Role: Methodology
                Role: MethodologyRole: SupervisionRole: Writing - review & editing
                Role: SupervisionRole: Writing - review & editing
                Role: Associate Editor
                Journal
                Bioinformatics
                Bioinformatics
                bioinformatics
                Bioinformatics
                Oxford University Press
                1367-4803
                1367-4811
                July 2024
                04 July 2024
                04 July 2024
                : 40
                : 7
                : btae438
                Affiliations
                School of Data Science and Artificial Intelligence, Wenzhou University of Technology , Wenzhou 325027, China
                College of Computer Science and Electronic Engineering, Hunan University , Changsha 410012, China
                School of Data Science and Artificial Intelligence, Wenzhou University of Technology , Wenzhou 325027, China
                School of Data Science and Artificial Intelligence, Wenzhou University of Technology , Wenzhou 325027, China
                Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China , Chengdu 611730, China
                Author notes
                Corresponding authors. School of Data Science and Artificial Intelligence, Wenzhou University of Technology,  No. 337, Jinhai 3rd Road, Wenzhou 325027, China. E-mail: zhuoninnin@ 123456163.com (L.Z.); Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 611730, China. E-mail: zouquan@ 123456nclab.net (Q.Z.)

                Xinqian Ma and Xiangzheng Fu Equal contribution.

                Author information
                https://orcid.org/0000-0001-6840-2573
                https://orcid.org/0000-0002-6586-0533
                https://orcid.org/0000-0001-6406-1142
                Article
                btae438
                10.1093/bioinformatics/btae438
                11245318
                38967119
                b4109a42-e414-448c-b282-9e56fc7d8ba7
                © The Author(s) 2024. Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 April 2024
                : 12 June 2024
                : 01 July 2024
                : 03 July 2024
                : 12 July 2024
                Page count
                Pages: 7
                Funding
                Funded by: National Natural Science Foundation of China, DOI 10.13039/501100001809;
                Award ID: 62302339
                Award ID: 62372158
                Categories
                Original Paper
                Sequence Analysis
                AcademicSubjects/SCI01060

                Bioinformatics & Computational biology
                Bioinformatics & Computational biology

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