多任务图深度学习模型,用于预测协同作用和敏感性得分的药物组合。

IF 2.9 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Samar Monem, Aboul Ella Hassanien, Alaa H Abdel-Hamid
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引用次数: 0

摘要

背景:事实证明,联合用药是治疗癌症等具有挑战性疾病的现实技术,既能提高疗效,又能减轻副作用。为了实现这些联合疗法的治疗目标,必须采用多靶点药物组合,以最大限度地提高疗效和协同效应:本文提出的 "MultiComb "是一种多任务深度学习(MTDL)模型,旨在同时预测药物组合的协同作用和敏感性。该模型利用图卷积网络来表示两种药物的简化分子输入线段(SMILES),生成它们各自的特征。此外,三个完全连接的子网络还能提取癌细胞系的特征。然后,这些药物和细胞系特征被连接起来,并通过注意力机制进行处理,从而为目标任务输出两个优化的特征表示。交叉缝合模型学习这些任务之间的关系。最后,将每个学习到的任务特征输入全连接子网络,以预测协同性和敏感性得分。我们使用 O'Neil 基准数据集对所提出的模型进行了验证,该数据集包含 38 种独特的药物,组合成 17,901 对药物组合,并在 37 种独特的癌细胞中进行了测试。该模型的性能测试采用了一些指标,如均方误差(MSE)、平均绝对误差(MAE)、决定系数(R 2)、斯皮尔曼和皮尔逊评分。在上述指标中,拟议模型的平均协同得分分别为 232.37、9.59、0.57、0.76 和 0.73。此外,平均灵敏度得分分别为 15.59、2.74、0.90、0.95 和 0.95:本文提出了一种 MTDL 模型,用于预测针对特定癌细胞系的药物组合的协同作用和敏感性得分。与现有方法相比,MTDL 模型表现出更优越的性能,提供了更好的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A multi-task graph deep learning model to predict drugs combination of synergy and sensitivity scores.

Background: Drug combination treatments have proven to be a realistic technique for treating challenging diseases such as cancer by enhancing efficacy and mitigating side effects. To achieve the therapeutic goals of these combinations, it is essential to employ multi-targeted drug combinations, which maximize effectiveness and synergistic effects.

Results: This paper proposes 'MultiComb', a multi-task deep learning (MTDL) model designed to simultaneously predict the synergy and sensitivity of drug combinations. The model utilizes a graph convolution network to represent the Simplified Molecular-Input Line-Entry (SMILES) of two drugs, generating their respective features. Also, three fully connected subnetworks extract features of the cancer cell line. These drug and cell line features are then concatenated and processed through an attention mechanism, which outputs two optimized feature representations for the target tasks. The cross-stitch model learns the relationship between these tasks. At last, each learned task feature is fed into fully connected subnetworks to predict the synergy and sensitivity scores. The proposed model is validated using the O'Neil benchmark dataset, which includes 38 unique drugs combined to form 17,901 drug combination pairs and tested across 37 unique cancer cells. The model's performance is tested using some metrics like mean square error ( MSE ), mean absolute error ( MAE ), coefficient of determination ( R 2 ), Spearman, and Pearson scores. The mean synergy scores of the proposed model are 232.37, 9.59, 0.57, 0.76, and 0.73 for the previous metrics, respectively. Also, the values for mean sensitivity scores are 15.59, 2.74, 0.90, 0.95, and 0.95, respectively.

Conclusion: This paper proposes an MTDL model to predict synergy and sensitivity scores for drug combinations targeting specific cancer cell lines. The MTDL model demonstrates superior performance compared to existing approaches, providing better results.

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来源期刊
BMC Bioinformatics
BMC Bioinformatics 生物-生化研究方法
CiteScore
5.70
自引率
3.30%
发文量
506
审稿时长
4.3 months
期刊介绍: BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology. BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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