ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025
A Network-Driven Framework for Drug Response Precision Prediction of Acute Myeloid Leukemia.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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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.
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.
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Who cites it
5 citing papers in PubMed.
- TargetPrior: a miRNA-signature embedded evolutionary learning framework for prioritizing drug targets in acute myeloid leukemia.Bioinformatics (Oxford, England) · 2026Article
- Putting the I in AML: Artificial Intelligence and Machine Learning in Acute Myeloid Leukemia.Cells · 2026Review
- Artificial Intelligence for Personalized Management of Acute Myeloid Leukemia.Journal of personalized medicine · 2026Review
- Pediatric leukemia: origins, pathogenesis, the role of microenvironment and immunological modulation.Frontiers in immunology · 2026Review
- A Network-Driven Framework for Drug Response Precision Prediction of Acute Myeloid Leukemia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
Acute myeloid leukemia (AML) is a clonal malignancy of myeloid progenitor cells that demonstrates highly variable responses to current regimens, highlighting the need for precision medicine. However, reliable biomarkers for precision medicine treatment remain elusive due to cellular heterogeneity. Conventional Models based on bulk RNA sequencing and ex vivo assays often fail to capture the intricate molecular pathways and gene networks that underlie treatment response and resistance. Here, NetAML, a novel network-based precision medicine platform that systematically develops 87 drug sensitivity prediction models for 87 clinical drugs using ex vivo drug responses from 520 AML patients with RNA-Seq is presented. The approach leverages network-based analysis and machine learning to identify biologically interpretable gene signatures that capture the complex molecular interactions driving differential drug responses. Notably, the signature genes derived from the models reveal distinct cellular mechanisms. For instance, the co-expression of C19ORF59 and FLT3 is associated with resistance to FLT3 inhibitors. In summary, NetAML offers a powerful strategy for personalized AML treatment by constructing drug-specific models, identifying clinically actionable biomarkers, and supporting the development of optimized, patient-specific therapeutic regimens.
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Registered trials
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.