Evidence map›Paper›PMID 42304175›Full record

ArticleBMC bioinformatics2026

drGT: interpretable drug response prediction with attention-guided gene attribution on a drug-cell-gene heterogeneous graph.

Yoshitaka Inoue, Hunmin Lee, Tianfan Fu, Rui Kuang, Augustin Luna

Abstract read
In one paragraph

Article in BMC bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yoshitaka InoueDepartment of Computer Science and Engineering, University of Minnesota, 200 Union Street SE, Minneapolis, MN, 55455, USA.
Hunmin LeeDepartment of Computer Science and Engineering, University of Minnesota, 200 Union Street SE, Minneapolis, MN, 55455, USA.
Tianfan FuSchool of Computer Science, Nanjing University, 22 Hankou Road, Nanjing, 210093, Jiangsu, China.
Rui KuangDepartment of Computer Science and Engineering, University of Minnesota, 200 Union Street SE, Minneapolis, MN, 55455, USA.
Augustin LunaComputational Biology Branch, National Library of Medicine, 8600 Rockville Pike, Bethesda, MD, 20894, USA. augustin@nih.gov.

Funding

Computational Analysis of Drug Response in Biological NetworksZIALM240126 · NLM · NATIONAL LIBRARY OF MEDICINE · PI LUNA, AUGUSTIN · 2024 to 2025
$1.8M
Intramural NIH HHS ZIA LM240126NLM NIH HHS ZIALM240126
6 · The paper itself

Abstract

backgroundFor translational impact, both accurate drug response prediction and biological plausibility of predictive features are needed. We present drGT, a heterogeneous graph deep learning model over drugs, genes, and cell lines that couples prediction with mechanism-oriented interpretability via attention coefficients (ACs).

resultsWe assess both predictive generalization (random, unseen-drug, unseen-cell, and zero-shot splits) and biological plausibility (use of text-mined PubMed gene-drug co-mentions and comparison to a structure-based DTI predictor) on GDSC, NCI60, and CTRP datasets. Across benchmarks, drGT consistently delivers top regression performance while maintaining competitive classification accuracy for drug sensitivity. Under random 5-fold cross-validation, drGT attains an AUROC of up to 0.945 (3rd overall) and an [Formula: see text] up to 0.690, outperforming all baselines on regression. In leave-one-out tests for unseen cell lines and drugs, drGT achieves AUROCs of 0.706 and 0.844, and [Formula: see text] values of 0.692 and 0.022, the only model yielding positive [Formula: see text] for unseen drugs. In zero-shot prediction, drGT achieves an AUROC of 0.786 and a regression [Formula: see text] of 0.334, both representing the highest scores among all models. For interpretability, AC-derived drug-gene links recover known biology: among 976 drugs with known DTIs, 36.9% of predicted links match established DTIs, and 63.7% are supported by either PubMed abstracts or a structure-based predictive model. Enrichment analyses of AC-prioritized genes reveal drug-perturbed biological processes, providing pathway-level explanations.

conclusionsdrGT advances predictive generalization and mechanism-centered interpretability, offering state-of-the-art regression accuracy and literature-supported biological hypotheses that demonstrate the use of graph learning from heterogeneous input data for biological discovery. Code: https://github.com/sciluna/drGT .

Indexed as

Computational BiologyDeep LearningHumansDrug response predictionGraph neural networksHeterogeneous networksInterpretability

Identifiers

PMID42304175
PMCPMC13523525

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.