Zero-shot Learning of Drug Response Prediction for Preclinical Drug Screening
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Abstract (arXiv)
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.
Key facts. Cited by 1 paper in the map (data through 14 Oct 2026). Builds on 16 of its 54 references that are in the map. First posted on arXiv 5 Oct 2023.
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16 of 54 references.
References · 16
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4 more
- 2021Regressive Domain Adaptation for Unsupervised Keypoint Detectioncited by 34
- 2020Unsupervised Domain Adaptation of a Pretrained Cross-Lingual Language Modelcited by 24
- 2018Drug cell line interaction predictioncited by 8
- 2022Towards a Better Model with Dual Transformer for Drug Response Predictioncited by 2
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Citing papers per year: 2023: 1.
1 paper.