Zero-shot Learning of Drug Response Prediction for Preclinical Drug Screening

Kun Li, Yong Luo, Xiantao Cai, Wenbin Hu, Bo Du
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Abstract

Conventional deep learning methods typically employ supervised learning for drug response prediction (DRP). This entails dependence on labeled response data from drugs for model training. However, practical applications in the preclinical drug screening phase demand that DRP models predict responses for novel compounds, often with unknown drug responses. This presents a challenge, rendering supervised deep learning methods unsuitable for such scenarios. In this paper, we propose a zero-shot learning solution for the DRP task in preclinical drug screening. Specifically, we propose a Multi-branch Multi-Source Domain Adaptation Test Enhancement Plug-in, called MSDA. MSDA can be seamlessly integrated with conventional DRP methods, learning invariant features from the prior response data of similar drugs to enhance real-time predictions of unlabeled compounds. We conducted experiments using the GDSCv2 and CellMiner datasets. The results demonstrate that MSDA efficiently predicts drug responses for novel compounds, leading to a general performance improvement of 5-10\% in the preclinical drug screening phase. The significance of this solution resides in its potential to accelerate the drug discovery process, improve drug candidate assessment, and facilitate the success of drug discovery.
临床前药物筛选中药物反应预测的零学习
传统的深度学习方法通常采用监督学习进行药物反应预测(DRP)。这就需要依赖药物的标记反应数据来进行模型训练。然而,在临床前药物筛选阶段的实际应用需要DRP模型预测新化合物的反应,通常是未知的药物反应。这提出了一个挑战,使监督深度学习方法不适合这种情况。本文针对临床前药物筛选中的DRP任务,提出了一种零机会学习解决方案。具体来说,我们提出了一个多分支多源域适应测试增强插件,称为MSDA。MSDA可以与传统的DRP方法无缝集成,从类似药物的先前反应数据中学习不变特征,以增强对未标记化合物的实时预测。我们使用gdscv2和CellMiner数据集进行了实验。结果表明,MSDA有效地预测了新化合物的药物反应,导致临床前药物筛选阶段的总体性能提高5- 10%。该解决方案的意义在于它有可能加速药物发现过程,改进候选药物评估,并促进药物发现的成功。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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