Condition-matched in silico prediction of drug transcriptional responses enables mechanism-guided screening and combination discovery

Perturbational transcriptomics links therapeutic compounds to cellular mechanisms and provides a powerful framework for drug discovery, but experimentally profiling transcriptional responses across diverse cell states, doses and durations is costly and often infeasible. Here we present DEPICT (Drug rEsponse Prediction in transCriptomics with Transformers), a deep learning framework that predicts condition-matched drug-induced transcriptional responses from baseline gene expression, perturbation settings and complementary drug representations. Using the LINCS L1000 dataset, DEPICT generalized to unseen drugs and cell types and outperformed five baseline strategies and two recent deep learning models. In the most challenging unseen-cell evaluation, DEPICT was the only model to surpass all baselines, improving differential-expression prediction accuracy and reducing perturbed-expression prediction error by 30.3% and 36.8%, respectively, relative to the next-best deep model. In a non-small cell lung cancer (NSCLC) case study, DEPICT-enabled virtual screening prioritized compounds predicted to reverse disease-associated transcriptional signatures. Notably, 13 of the top 20 prioritized compounds had either previously entered NSCLC-related clinical trials or been validated in NSCLC studies, supporting the translational relevance of the predicted perturbational profiles. DEPICT further enabled condition-matched drug synergy prediction and mechanistic exploration when experimentally matched profiles were unavailable. Together, these results show that accurate, condition-matched in silico perturbation profiling can scale transcriptomics-driven hypothesis generation for drug repurposing and combination discovery.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-03-31
DOI
https://doi.org/10.64898/2026.03.27.714886
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Condition-matched in silico prediction of drug transcriptional responses enables mechanism-guided screening and combination discovery

Fei Zou, Baiming Zou, Mei‐Sheng Xiao, Jianhua Hu et al.
bioRxiv (Cold Spring Harbor Laboratory)
Computational Drug Discovery Methods
article

Condition-matched in silico prediction of drug transcriptional responses enables mechanism-guided screening and combination discovery

Fei Zou, Baiming Zou, Mei‐Sheng Xiao, Jianhua Hu, Yiping He
article en

Abstract

Perturbational transcriptomics links therapeutic compounds to cellular mechanisms and provides a powerful framework for drug discovery, but experimentally profiling transcriptional responses across diverse cell states, doses and durations is costly and often infeasible. Here we present DEPICT (Drug rEsponse Prediction in transCriptomics with Transformers), a deep learning framework that predicts condition-matched drug-induced transcriptional responses from baseline gene expression, perturbation settings and complementary drug representations. Using the LINCS L1000 dataset, DEPICT generalized to unseen drugs and cell types and outperformed five baseline strategies and two recent deep learning models. In the most challenging unseen-cell evaluation, DEPICT was the only model to surpass all baselines, improving differential-expression prediction accuracy and reducing perturbed-expression prediction error by 30.3% and 36.8%, respectively, relative to the next-best deep model. In a non-small cell lung cancer (NSCLC) case study, DEPICT-enabled virtual screening prioritized compounds predicted to reverse disease-associated transcriptional signatures. Notably, 13 of the top 20 prioritized compounds had either previously entered NSCLC-related clinical trials or been validated in NSCLC studies, supporting the translational relevance of the predicted perturbational profiles. DEPICT further enabled condition-matched drug synergy prediction and mechanistic exploration when experimentally matched profiles were unavailable. Together, these results show that accurate, condition-matched in silico perturbation profiling can scale transcriptomics-driven hypothesis generation for drug repurposing and combination discovery.

bioRxiv (Cold Spring Harbor Laboratory)
University of North Carolina at Chapel Hill (US), Duke University (US), Duke Medical Center (US), Columbia University (US)
National Institutes of Health
Good health and well-being
Openalex Percentile: Top 23%
Computational Drug Discovery Methods
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