TAPB: an interventional debiasing framework for alleviating target prior bias in drug-target interaction prediction

Drug Target Interaction (DTI) prediction is vital for drug repurposing. Previous DTI studies on BioSNAP and BindingDB datasets often attribute biased predictions to "drug bias," while our work reveals "target prior bias" as the predominant issue. This bias stems from the "prior tendency," characterized by the imbalanced label distribution of targets in the training data. From causal lens, target "prior tendency" is a confounder, causing models trained with P(Y∣D, T) to learn spurious associations between targets and labels rather than genuine interaction mechanisms. In this study, we introduce alleviating Target Prior Bias in Drug-Target Interaction Prediction (TAPB), a novel debiasing framework that employs amino acid randomization, confounder alignment module (CAM), and interventional training to compute P(Y∣D, do(T)) via backdoor adjustment, thereby addressing this bias. TAPB achieves competitive performance over existing approaches, demonstrating enhanced generalization and providing interpretable insights into DTIs.

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Publication Details

Journal
Nature Communications
Published
2025-12-02
DOI
https://doi.org/10.1038/s41467-025-66915-1
Citations
1
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
1.50
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article

TAPB: an interventional debiasing framework for alleviating target prior bias in drug-target interaction prediction

Quan Zou, Yijie Ding, Zhong-Hao Ren, Changjun Zhou et al.
1 citations
Nature Communications
Computational Drug Discovery Methods
1.50
article

TAPB: an interventional debiasing framework for alleviating target prior bias in drug-target interaction prediction

Quan Zou, Yijie Ding, Zhong-Hao Ren, Changjun Zhou, Prayag Tiwari, Xin Zhang, Gaoming Lin
article en
1 citations

Abstract

Drug Target Interaction (DTI) prediction is vital for drug repurposing. Previous DTI studies on BioSNAP and BindingDB datasets often attribute biased predictions to "drug bias," while our work reveals "target prior bias" as the predominant issue. This bias stems from the "prior tendency," characterized by the imbalanced label distribution of targets in the training data. From causal lens, target "prior tendency" is a confounder, causing models trained with P(Y∣D, T) to learn spurious associations between targets and labels rather than genuine interaction mechanisms. In this study, we introduce alleviating Target Prior Bias in Drug-Target Interaction Prediction (TAPB), a novel debiasing framework that employs amino acid randomization, confounder alignment module (CAM), and interventional training to compute P(Y∣D, do(T)) via backdoor adjustment, thereby addressing this bias. TAPB achieves competitive performance over existing approaches, demonstrating enhanced generalization and providing interpretable insights into DTIs.

Nature CommunicationsVol. 16(1)
Zhejiang Normal University (CN), University of Electronic Science and Technology of China (CN), Hunan University (CN), Wenzhou Medical University (CN), Ministry of Education (SA), Quzhou University (CN), Halmstad University (SE)
Openalex Percentile: Top 12%
Computational Drug Discovery Methods
1.50
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