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

Kun Li, Yong Luo, Xiantao Cai, Wenbin Hu, Bo Du
{"title":"Zero-shot Learning of Drug Response Prediction for Preclinical Drug Screening","authors":"Kun Li, Yong Luo, Xiantao Cai, Wenbin Hu, Bo Du","doi":"arxiv-2310.12996","DOIUrl":null,"url":null,"abstract":"Conventional deep learning methods typically employ supervised learning for\ndrug response prediction (DRP). This entails dependence on labeled response\ndata from drugs for model training. However, practical applications in the\npreclinical drug screening phase demand that DRP models predict responses for\nnovel compounds, often with unknown drug responses. This presents a challenge,\nrendering supervised deep learning methods unsuitable for such scenarios. In\nthis paper, we propose a zero-shot learning solution for the DRP task in\npreclinical drug screening. Specifically, we propose a Multi-branch\nMulti-Source Domain Adaptation Test Enhancement Plug-in, called MSDA. MSDA can\nbe seamlessly integrated with conventional DRP methods, learning invariant\nfeatures from the prior response data of similar drugs to enhance real-time\npredictions of unlabeled compounds. We conducted experiments using the GDSCv2\nand CellMiner datasets. The results demonstrate that MSDA efficiently predicts\ndrug responses for novel compounds, leading to a general performance\nimprovement of 5-10\\% in the preclinical drug screening phase. The significance\nof this solution resides in its potential to accelerate the drug discovery\nprocess, improve drug candidate assessment, and facilitate the success of drug\ndiscovery.","PeriodicalId":501321,"journal":{"name":"arXiv - QuanBio - Cell Behavior","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Cell Behavior","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2310.12996","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Persistent pseudopod splitting is an effective chemotaxis strategy in shallow gradients Geometric Effects in Large Scale Intracellular Flows Motion Ordering in Cellular Polar-polar and Polar-nonpolar Interactions Modelling how lamellipodia-driven cells maintain persistent migration and interact with external barriers Synchronized Memory-Dependent Intracellular Oscillations for a Cell-Bulk ODE-PDE Model in $\mathbb{R}^2$
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1