Evidence map›Paper›PMID 40918644›Full record

ArticleNAR cancer2025

Neural interaction explainable AI predicts drug response across cancers.

Philipp Keyl, Julius Keyl, Andreas Mock, Gabriel Dernbach, Liliana H Mochmann, Niklas Kiermeyer, Philipp Jurmeister, Michael Bockmayr, Roland F Schwarz, Grégoire Montavon and 2 more

Abstract read
In one paragraph

Article in NAR cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Philipp KeylInstitute of Pathology, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-5472-4683
Julius KeylInstitute for Artificial Intelligence in Medicine, University Hospital Essen (AöR), Essen, Germany.ORCID 0000-0002-5617-091X
Andreas MockInstitute of Pathology, Faculty of Medicine, LMU Munich, 80337 Munich, Germany.
Gabriel DernbachMachine Learning Group, Technical University of Berlin, 10587 Berlin, Germany.
Liliana H MochmannInstitute of Pathology, Faculty of Medicine, LMU Munich, 80337 Munich, Germany.
Niklas KiermeyerInstitute of Pathology, Faculty of Medicine, LMU Munich, 80337 Munich, Germany.
Philipp JurmeisterInstitute of Pathology, Faculty of Medicine, LMU Munich, 80337 Munich, Germany.
Michael BockmayrInstitute of Pathology, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-9249-4292
Roland F SchwarzBIFOLD-Berlin Institute for the Foundations of Learning and Data, 10587 Berlin, Germany.
Grégoire MontavonBIFOLD-Berlin Institute for the Foundations of Learning and Data, 10587 Berlin, Germany.ORCID 0000-0001-7243-6186
Klaus-Robert MüllerBIFOLD-Berlin Institute for the Foundations of Learning and Data, 10587 Berlin, Germany.ORCID 0000-0002-3861-7685
Frederick KlauschenInstitute of Pathology, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.ORCID 0000-0002-9131-2389

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Personalized treatment selection is crucial for cancer patients due to the high variability in drug response. While actionable mutations can increasingly inform treatment decisions, most therapies still rely on population-based approaches. Here, we introduce neural interaction explainable AI (NeurixAI), an explainable and highly scalable deep learning framework that models drug-gene interactions and identifies transcriptomic patterns linked with drug response. Trained on data from 546 646 drug perturbation experiments involving 1135 drugs and molecular profiles from 476 tumors, NeurixAI accurately predicted treatment responses for 272 targeted and 30 chemotherapeutic drugs in unseen tumor samples (Spearman's rho >0.2), maintaining high performance on an external validation set. Additionally, NeurixAI identified the anticancer potential of 160 repurposed non-cancer drugs. Using explainable artificial intelligence (xAI), our framework uncovered key genes influencing drug response at the individual tumor level and revealed both known and novel mechanisms of drug resistance. These findings demonstrate the potential of integrating transcriptomics with xAI to optimize cancer treatment, enable drug repurposing, and identify new therapeutic targets.

Indexed as

Antineoplastic AgentsArtificial IntelligenceNeoplasmsDeep LearningDrug RepositioningDrug Resistance, NeoplasmGene Expression ProfilingHumansPrecision MedicineTranscriptomeAntineoplastic Agents

Identifiers

PMID40918644
PMCPMC12409417

What OpenQuestion holds

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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.