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Updated: Jan 15, 2026

Author Spotlight: Establishment of Pancreatic Cancer-Derived Tumor Organoids and Fibroblasts From Fresh Tissue
Published on: May 26, 2023
Advances in precision oncology using patient-derived organoids and functional biomaterials
Hina Singh1, Ivan Mijakovic2,3, Priyanka Singh2
1Division of Biomedical Sciences, School of Medicine, University of California, Riverside, Riverside, CA, United States.
Abstract:
Despite major advances in oncology, cancer therapy continues to face persistent challenges due to intratumoral heterogeneity, drug resistance, and the poor clinical translation of experimental therapeutics. Conventional preclinical models such as 2D cultures and animal systems often fail to accurately recapitulate the tumor microenvironment immune contexture, and patient-specific variability limiting their predictive power. While nanomedicine and advanced drug delivery platforms offer promising solutions, their translational success is hindered by insufficient integration with physiologically relevant tumor models. In this review, we critically examine how patient-derived organoids derived from patient tumors serve as next-generation platforms for modeling cancer heterogeneity, therapeutic response, and biomarker discovery. We further explore how the integration of PDOs with functional biomaterials, extracellular matrix mimetics, and organ-on-chip systems enables dynamic co-culture environments that capture tumor-stroma-immune interactions with high fidelity. By linking the biological underpinnings of resistance, such as genetic mutations, altered signaling, metabolic rewiring, and immune evasion, with smart biomaterial design and drug screening workflows, we propose a unified roadmap for precision oncology. Additionally, we highlight the emergence of PDO biobanks, co-culture innovations, and high-throughput phenotypic screening as essential tools for improving clinical translation. This interdisciplinary synthesis underscores the transformative potential of PDO-based platforms in accelerating personalized cancer therapy.
Insights
Patient-derived organoids (PDOs) offer a powerful new way to study cancer. Integrating PDOs with advanced biomaterials and organ-on-chip systems accelerates precision oncology by improving drug screening and clinical translation.
Area of Science:
- Oncology
- Biomaterials Science
- Translational Medicine
Background:
- Cancer therapy faces challenges from tumor heterogeneity, drug resistance, and poor translation of experimental treatments.
- Traditional models like 2D cultures and animal systems lack accuracy in mimicking the tumor microenvironment and patient variability.
- Nanomedicine and advanced drug delivery face hurdles due to insufficient integration with relevant tumor models.
Purpose of the Study:
- To review patient-derived organoids (PDOs) as next-generation platforms for cancer research.
- To explore the integration of PDOs with biomaterials and organ-on-chip systems for modeling tumor microenvironments.
- To propose a roadmap for precision oncology by linking resistance mechanisms with advanced modeling and drug screening.
Main Methods:
- Critical examination of PDOs for modeling cancer heterogeneity, therapeutic response, and biomarker discovery.
- Exploration of PDO integration with functional biomaterials, extracellular matrix mimetics, and organ-on-chip systems.
- Synthesis of biological resistance mechanisms with biomaterial design and drug screening workflows.
Main Results:
- PDOs serve as advanced platforms for modeling cancer heterogeneity and response.
- Integrated PDO systems capture high-fidelity tumor-stroma-immune interactions.
- PDO biobanks, co-culture innovations, and high-throughput screening enhance clinical translation.
Conclusions:
- PDO-based platforms offer transformative potential for personalized cancer therapy.
- Integrating PDOs with advanced technologies addresses limitations of conventional preclinical models.
- This approach accelerates the development and clinical application of precision oncology treatments.
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