MultiCTox: Empowering Accurate Cardiotoxicity Prediction through Adaptive Multimodal Learning

IF 5.6 2区 化学 Q1 CHEMISTRY, MEDICINAL
Lin Feng, Xiangzheng Fu, Zhenya Du, Yuting Guo, Linlin Zhuo*, Yan Yang, Dongsheng Cao* and Xiaojun Yao*, 
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引用次数: 0

Abstract

Cardiotoxicity refers to the inhibitory effects of drugs on cardiac ion channels. Accurate prediction of cardiotoxicity is crucial yet challenging, as it directly impacts the evaluation of cardiac drug efficacy and safety. Numerous methods have been developed to predict cardiotoxicity, yet their performance remains limited. A key limitation is that these methods often rely solely on single-modal data, making multimodal data integration challenging. As a result, we present a multimodal method integrating molecular SMILES, structure, and fingerprint to enhance cardiotoxicity prediction. First, we designed a fusion layer to unify representations from different modalities. During training, the model maximizes intramodal similarity for the same molecule while minimizing intermolecular similarity, ensuring consistent cross-modal representations. This study evaluates the inhibitory effects of candidate drugs on voltage-gated potassium (hERG), sodium (Nav1.5), and calcium (Cav1.2) channels. Experimental results demonstrate that the proposed model significantly outperforms existing state-of-the-art methods in cardiotoxicity prediction. We anticipate that this model will contribute significantly to the development and safety evaluation of cardiac drugs, reducing cardiotoxicity-related risks.

Abstract Image

MultiCTox:通过自适应多模态学习实现准确的心脏毒性预测
心脏毒性是指药物对心脏离子通道的抑制作用。准确预测心脏毒性至关重要,但也极具挑战性,因为它直接影响到心脏药物疗效和安全性的评估。目前已开发出许多预测心脏毒性的方法,但其性能仍然有限。一个关键的局限是,这些方法通常仅依赖于单模态数据,这使得多模态数据整合具有挑战性。因此,我们提出了一种整合分子 SMILES、结构和指纹的多模态方法来增强心脏毒性预测。首先,我们设计了一个融合层来统一来自不同模态的表征。在训练过程中,该模型将同一分子的模内相似度最大化,同时将分子间相似度最小化,从而确保跨模态表征的一致性。本研究评估了候选药物对电压门控钾(hERG)、钠(Nav1.5)和钙(Cav1.2)通道的抑制作用。实验结果表明,在心脏毒性预测方面,所提出的模型明显优于现有的最先进方法。我们预计该模型将极大地促进心脏病药物的开发和安全性评估,降低与心脏毒性相关的风险。
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来源期刊
CiteScore
9.80
自引率
10.70%
发文量
529
审稿时长
1.4 months
期刊介绍: The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery. Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field. As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.
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