AlJarf Raghad, Rodrigues Carlos H M, Myung Yoochan, Pires Douglas E V, Ascher David B
Structural Biology and Bioinformatics, Department of Biochemistry and Pharmacology, University of Melbourne, Melbourne, VIC, Australia.
Systems and Computational Biology, Bio21 Institute, University of Melbourne, Melbourne, VIC, Australia.
J Cheminform. 2024 Jul 19;16(1):81. doi: 10.1186/s13321-024-00859-4.
While drug combination therapies are of great importance, particularly in cancer treatment, identifying novel synergistic drug combinations has been a challenging venture. Computational methods have emerged in this context as a promising tool for prioritizing drug combinations for further evaluation, though they have presented limited performance, utility, and interpretability. Here, we propose a novel predictive tool, piscesCSM, that leverages graph-based representations to model small molecule chemical structures to accurately predict drug combinations with favourable anticancer synergistic effects against one or multiple cancer cell lines. Leveraging these insights, we developed a general supervised machine learning model to guide the prediction of anticancer synergistic drug combinations in over 30 cell lines. It achieved an area under the receiver operating characteristic curve (AUROC) of up to 0.89 on independent non-redundant blind tests, outperforming state-of-the-art approaches on both large-scale oncology screening data and an independent test set generated by AstraZeneca (with more than a 16% improvement in predictive accuracy). Moreover, by exploring the interpretability of our approach, we found that simple physicochemical properties and graph-based signatures are predictive of chemotherapy synergism. To provide a simple and integrated platform to rapidly screen potential candidate pairs with favourable synergistic anticancer effects, we made piscesCSM freely available online at https://biosig.lab.uq.edu.au/piscescsm/ as a web server and API. We believe that our predictive tool will provide a valuable resource for optimizing and augmenting combinatorial screening libraries to identify effective and safe synergistic anticancer drug combinations. SCIENTIFIC CONTRIBUTION: This work proposes piscesCSM, a machine-learning-based framework that relies on well-established graph-based representations of small molecules to identify and provide better predictive accuracy of syngenetic drug combinations. Our model, piscesCSM, shows that combining physiochemical properties with graph-based signatures can outperform current architectures on classification prediction tasks. Furthermore, implementing our tool as a web server offers a user-friendly platform for researchers to screen for potential synergistic drug combinations with favorable anticancer effects against one or multiple cancer cell lines.
虽然联合药物疗法非常重要,尤其是在癌症治疗中,但确定新的协同药物组合一直是一项具有挑战性的工作。在这种情况下,计算方法已成为一种很有前景的工具,可用于对药物组合进行优先级排序以便进一步评估,不过它们的性能、实用性和可解释性都很有限。在此,我们提出了一种新型预测工具piscesCSM,它利用基于图的表示法对小分子化学结构进行建模,以准确预测对一种或多种癌细胞系具有良好抗癌协同效应的药物组合。利用这些见解,我们开发了一个通用的监督机器学习模型,以指导在30多种细胞系中预测抗癌协同药物组合。在独立的非冗余盲测中,它在受试者工作特征曲线下面积(AUROC)高达0.89,在大规模肿瘤学筛查数据和阿斯利康生成的独立测试集上均优于现有方法(预测准确率提高超过16%)。此外,通过探索我们方法的可解释性,我们发现简单的物理化学性质和基于图的特征可预测化疗协同作用。为了提供一个简单且集成的平台,以快速筛选具有良好协同抗癌效应的潜在候选药物对,我们将piscesCSM作为网络服务器和应用程序编程接口免费在线提供,网址为https://biosig.lab.uq.edu.au/piscescsm/。我们相信,我们的预测工具将为优化和扩充组合筛选文库以识别有效且安全的协同抗癌药物组合提供有价值的资源。科学贡献:这项工作提出了piscesCSM,这是一个基于机器学习的框架,它依赖于成熟的小分子基于图的表示法来识别并提供更好的合成药物组合预测准确性。我们的模型piscesCSM表明,将物理化学性质与基于图的特征相结合在分类预测任务上可优于当前架构。此外,将我们的工具实现为网络服务器为研究人员提供了一个用户友好的平台,用于筛选对一种或多种癌细胞系具有良好抗癌效应的潜在协同药物组合。