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Biology subjects

Nees, M.

Publications and source records attributed to Nees, M..

2 recordsLinked to original sources

A Patient-Derived Scaffold-Based 3D Culture Platform for Head and Neck Cancer: Preserving Tumor Heterogeneity for Personalized Drug Testing

Standard 3-D models for head-and-neck cancer (HNC) often lose stromal partners that influence drug response or never include them. We developed a patient-derived cell culture system that maintains tumor cells, cancer-associated fibroblasts (CAFs), and cells undergoing partial epithelial-to-mesenchymal transition (pEMT) for rapid sensitivity testing. Biopsies from four HNC patients were enzymatically dissociated. CAFs were directly cultured, and their conditioned medium (CAF-CM) was collected. Cryopreserved tumour cell suspensions were later revived, screened in five different growth media in 2-D conditions, and the most heterogeneous cultures were re-embedded in 3-D hydrogels with varied gel mix, medium, and seeding geometry. A perimeter-derived complexity index was used to quantify tumoroid morphology and viability after exposure to cisplatin or the Notch modulators RIN-1 (activator) and FLI-06 (inhibitor), which were assessed by live imaging and WST-8 assays. ECM-2 medium alone produced compact CAF-free spheroids, whereas ECM-2 supplemented with CAF medium generated invasive aggregates that deposited endogenous matrix; Matrigel plus this medium and single-point seeding yielded the highest complexity scores. Two of the three patient tumoroids were cisplatin-sensitive, and all showed significant growth inhibition with the FLI-06 inhibitor, while RIN-1 induced minimal change. The optimised scaffold retains tumour-stroma cross-talk and affords patient-specific drug-response data within days, supporting personalised treatment selection in HNC.

cancer biology↗

Genipin-Crosslinked, Silane-Anchored 3D Tumor-Stroma Microtissues for High-Content On-Chip Drug Testing

Physiologically relevant 3D tumor models incorporating extracellular matrix (ECM) and cancer-associated fibroblasts (CAFs) are essential for studying tumor progression and drug resistance yet often suffer from hydrogel contraction and instability - especially in microfluidic formats, where ECM deformation hampers long-term culture and quantitative imaging. Here, we present a microfluidic tumor-stroma co-culture platform for head and neck squamous cell carcinoma (HNSCC) that overcomes these limitations through a dual-material strategy: APTES-mediated surface silanization anchors the ECM to the chip, while Genipin-based crosslinking enhances matrix stiffness without compromising cell viability. This approach stabilizes collagen-rich hydrogels for over 10 days, preserving 3D architecture, sustaining >85% viability, and supporting active proliferation. Fourier-transform infrared spectroscopy (FTIR) confirmed successful collagen crosslinking, combining covalent modification of biomaterials with improved mechanical performance. The platform further integrates AI-assisted, high-content imaging to quantify dynamic phenotypic drug responses at both single-cell and higher multicellular/tissue level resolution. Drug chemosensitivity assays, including the co-culture of tumor cells with patient-derived CAFs, demonstrated the quantitative assessment of clinically relevant chemoprotective effects. By combining biomaterial engineering with functional microfluidic design, this system enables reproducible, physiologically relevant modeling of tumor-stroma interactions, offering a scalable tool for preclinical drug screening and personalized medicine or precision oncology applications.

bioengineering↗