ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Deep Learning-Powered Scalable Cancer Organ Chip for Cancer Precision Medicine.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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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.
Who cites it
5 citing papers in PubMed.
- Evaluating Alternatives to Fetal Bovine Serum in the Development of Advanced Biomaterial-Based Tumor Models: Overcoming Challenges in Biofabrication.Bioengineering (Basel, Switzerland) · 2026Article
- Macrophage-derived fibronectin suppresses antitumor immunity via tissue stiffening and immunosuppressive cell induction in cancer mouse models.Nature communications · 2026Article
- Harnessing Cancer Stem Cells and 3D Organoids in Unravelling Spatial and Cellular Heterogeneity in Cancer.International journal of molecular sciences · 2026Review
- Engineering Organ-on-a-Chip Systems for Cancer Immunotherapy: Strategies and Assay Integration.Bioengineering (Basel, Switzerland) · 2026Review
- Patient-derived organoids in gastric cancer: bridging the tumor microenvironment to functional precision oncology.Frontiers in bioengineering and biotechnology · 2026Review
Corrections and comments
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Authors and funding
25 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Functional precision oncology complements genomic approaches by directly testing treatment options on patient-derived models. However, existing platformssuch as patient-derived xenografts (PDXs) and patient-derived organoids (PDOs), face major barriers in clinical use due to technical challenges, including limited standardization, high costs, long assay times, scalability constraints, and incomplete recapitulation of the patient tumor microenvironment (TME). Here, we present a scalable, low-cost Organ Chip (OC) platform fabricated entirely from thermoplastics via injection molding. Leveraging a patented channel geometry and surface treatment, the device achieves barrier-free hydrogel confinement through capillary pinning without porous membranes, micropillars, or other barrier structures. This automation-compatible platform supports tissue-specific extracellular matrices and co-culture through versatile perfusion modes, with robust imaging compatibility. We demonstrate its feasibility for drug sensitivity testing using multiple cell lines and patient-derived primary cells, with imaging-based phenotypic profiling for accurate quantification of drug responses, closely aligning with clinical outcomes. Additionally, we integrated a deep learning-based image translation model that predicts fluorescence staining from bright-field images. This approach enables longitudinal, label-free phenotypic analysis with higher sensitivity than conventional endpoint staining. Together, this integrated cancer OC system overcomes key technical challenges and offers a promising framework for functional precision oncology through high-throughput, patient-relevant drug testing.
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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 Socratic graph.