TY - JOUR
T1 - scRADAR
T2 - Dissecting intratumoral drug response heterogeneity at single-cell resolution via mechanism-guided prototype routing
AU - Qi, Ren
AU - Teng, Wenjie
AU - Yang, Xin
AU - Han, Peng
AU - Shaytan, Alexey K.
AU - Liu, Bin
N1 - Publisher Copyright:
© 2026 Qi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. http://creativecommons.org/licenses/by/4.0/
PY - 2026/6
Y1 - 2026/6
N2 - Precision oncology requires resolving intratumoral heterogeneity to identify drug-resistant cell states associated with treatment failure and relapse. Although single-cell RNA sequencing enables characterization of heterogeneous resistance-associated states, single-cell drug-response phenotype prediction remains challenging because of sparsity, noise, class imbalance, and limited mechanistic interpretability. Here, we present scRADAR (Response Analysis via Drug-Aware Routing), a mechanism-guided prototype routing framework for predicting and interpreting drug-response phenotypes at single-cell resolution. Rather than relying on cell-line–anchored transfer learning, scRADAR learns directly from labeled single-cell cohorts. The framework integrates metabolic and signaling pathway activities to form a dual-view cellular representation, conditions pathway embeddings on drug mechanisms through feature-wise linear modulation, and uses sparse prototype routing to decompose predictions into interpretable response archetypes. Across nine independent cohorts, scRADAR showed strong predictive performance and consistent cross-cohort behavior, particularly under imbalanced settings. Post hoc attribution analyses highlighted candidate TGF-β-associated epithelial-to-mesenchymal transition signatures in Erlotinib-associated Resistant-labeled states and cytoskeletal/metabolic response-associated signatures in BET-inhibitor-associated Resistant-labeled states. These results suggest that scRADAR provides an interpretable framework for single-cell drug-response phenotype prediction and for generating hypotheses about resistance-associated programs from heterogeneous tumor transcriptomes.
AB - Precision oncology requires resolving intratumoral heterogeneity to identify drug-resistant cell states associated with treatment failure and relapse. Although single-cell RNA sequencing enables characterization of heterogeneous resistance-associated states, single-cell drug-response phenotype prediction remains challenging because of sparsity, noise, class imbalance, and limited mechanistic interpretability. Here, we present scRADAR (Response Analysis via Drug-Aware Routing), a mechanism-guided prototype routing framework for predicting and interpreting drug-response phenotypes at single-cell resolution. Rather than relying on cell-line–anchored transfer learning, scRADAR learns directly from labeled single-cell cohorts. The framework integrates metabolic and signaling pathway activities to form a dual-view cellular representation, conditions pathway embeddings on drug mechanisms through feature-wise linear modulation, and uses sparse prototype routing to decompose predictions into interpretable response archetypes. Across nine independent cohorts, scRADAR showed strong predictive performance and consistent cross-cohort behavior, particularly under imbalanced settings. Post hoc attribution analyses highlighted candidate TGF-β-associated epithelial-to-mesenchymal transition signatures in Erlotinib-associated Resistant-labeled states and cytoskeletal/metabolic response-associated signatures in BET-inhibitor-associated Resistant-labeled states. These results suggest that scRADAR provides an interpretable framework for single-cell drug-response phenotype prediction and for generating hypotheses about resistance-associated programs from heterogeneous tumor transcriptomes.
UR - https://www.scopus.com/pages/publications/105043876729
U2 - 10.1371/journal.pcbi.1014392
DO - 10.1371/journal.pcbi.1014392
M3 - Article
C2 - 42361193
AN - SCOPUS:105043876729
SN - 1932-6203
VL - 22
JO - PLoS ONE
JF - PLoS ONE
IS - 6
ER -