Lawrence Patrick J, Burns Benjamin, Ning Xia
Biomedical Informatics Department, The Ohio State University, 1800 Cannon Drive, Lincoln Tower 250, Columbus, OH, 43210, USA.
Computer Science and Engineering Department, The Ohio State University, 2015 Neil Avenue, Columbus, OH, 43210, USA.
NPJ Precis Oncol. 2024 May 18;8(1):106. doi: 10.1038/s41698-024-00589-8.
Due to cancer's complex nature and variable response to therapy, precision oncology informed by omics sequence analysis has become the current standard of care. However, the amount of data produced for each patient makes it difficult to quickly identify the best treatment regimen. Moreover, limited data availability has hindered computational methods' abilities to learn patterns associated with effective drug-cell line pairs. In this work, we propose the use of contrastive learning to improve learned drug and cell line representations by preserving relationship structures associated with drug mechanisms of action and cell line cancer types. In addition to achieving enhanced performance relative to a state-of-the-art method, we find that classifiers using our learned representations exhibit a more balanced reliance on drug- and cell line-derived features when making predictions. This facilitates more personalized drug prioritizations that are informed by signals related to drug resistance.
由于癌症的复杂性以及对治疗的可变反应,基于组学序列分析的精准肿瘤学已成为当前的治疗标准。然而,为每位患者生成的数据量使得快速确定最佳治疗方案变得困难。此外,有限的数据可用性阻碍了计算方法学习与有效药物 - 细胞系对相关模式的能力。在这项工作中,我们提出使用对比学习来通过保留与药物作用机制和细胞系癌症类型相关的关系结构来改进学习到的药物和细胞系表示。除了相对于一种先进方法实现性能增强外,我们发现使用我们学习到的表示的分类器在进行预测时对药物和细胞系衍生特征表现出更平衡的依赖。这有助于基于与耐药性相关的信号进行更个性化的药物优先级排序。