Ziyan Wang, Zhankun Xiong, Feng Huang, Xuan Liu, Wen Zhang
{"title":"ZeroDDI: A Zero-Shot Drug-Drug Interaction Event Prediction Method with Semantic Enhanced Learning and Dual-Modal Uniform Alignment","authors":"Ziyan Wang, Zhankun Xiong, Feng Huang, Xuan Liu, Wen Zhang","doi":"arxiv-2407.00891","DOIUrl":null,"url":null,"abstract":"Drug-drug interactions (DDIs) can result in various pharmacological changes,\nwhich can be categorized into different classes known as DDI events (DDIEs). In\nrecent years, previously unobserved/unseen DDIEs have been emerging, posing a\nnew classification task when unseen classes have no labelled instances in the\ntraining stage, which is formulated as a zero-shot DDIE prediction (ZS-DDIE)\ntask. However, existing computational methods are not directly applicable to\nZS-DDIE, which has two primary challenges: obtaining suitable DDIE\nrepresentations and handling the class imbalance issue. To overcome these\nchallenges, we propose a novel method named ZeroDDI for the ZS-DDIE task.\nSpecifically, we design a biological semantic enhanced DDIE representation\nlearning module, which emphasizes the key biological semantics and distills\ndiscriminative molecular substructure-related semantics for DDIE representation\nlearning. Furthermore, we propose a dual-modal uniform alignment strategy to\ndistribute drug pair representations and DDIE semantic representations\nuniformly in a unit sphere and align the matched ones, which can mitigate the\nissue of class imbalance. Extensive experiments showed that ZeroDDI surpasses\nthe baselines and indicate that it is a promising tool for detecting unseen\nDDIEs. Our code has been released in https://github.com/wzy-Sarah/ZeroDDI.","PeriodicalId":501022,"journal":{"name":"arXiv - QuanBio - Biomolecules","volume":"33 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Biomolecules","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2407.00891","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
Drug-drug interactions (DDIs) can result in various pharmacological changes,
which can be categorized into different classes known as DDI events (DDIEs). In
recent years, previously unobserved/unseen DDIEs have been emerging, posing a
new classification task when unseen classes have no labelled instances in the
training stage, which is formulated as a zero-shot DDIE prediction (ZS-DDIE)
task. However, existing computational methods are not directly applicable to
ZS-DDIE, which has two primary challenges: obtaining suitable DDIE
representations and handling the class imbalance issue. To overcome these
challenges, we propose a novel method named ZeroDDI for the ZS-DDIE task.
Specifically, we design a biological semantic enhanced DDIE representation
learning module, which emphasizes the key biological semantics and distills
discriminative molecular substructure-related semantics for DDIE representation
learning. Furthermore, we propose a dual-modal uniform alignment strategy to
distribute drug pair representations and DDIE semantic representations
uniformly in a unit sphere and align the matched ones, which can mitigate the
issue of class imbalance. Extensive experiments showed that ZeroDDI surpasses
the baselines and indicate that it is a promising tool for detecting unseen
DDIEs. Our code has been released in https://github.com/wzy-Sarah/ZeroDDI.