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Reszczynska, E.

Publications and source records attributed to Reszczynska, E..

3 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↗

Mechanisms shaping the synergism of zeaxanthin and PsbS in photoprotective energy dissipation in the photosynthetic apparatus of plants

Safe operation of photosynthesis is vital to plants and is ensured by the activity of numerous processes protecting chloroplasts against photo-damage. The harmless dissipation of excess excitation energy is believed to be the main photoprotective mechanism and is most effective with the simultaneous presence of PsbS protein and zeaxanthin, a xanthophyll accumulated in strong light as a result of the xanthophyll cycle activity. Here we address the problem of specific molecular mechanisms underlying the synergistic effect of zeaxanthin and PsbS. The experiments were conducted with Arabidopsis thaliana, the wild-type and the mutants lacking PsbS (npq4) and affected in the xanthophyll cycle (npq1), with the application of multiple molecular spectroscopy and imaging techniques. Research results lead to the conclusion that PsbS interferes with the formation of tightly packed aggregates of thylakoid membrane proteins, thus enabling the incorporation of xanthophyll cycle pigments into such structures. It was found that xanthophylls trapped within supramolecular structures, most likely in the interfacial protein region, determine their photophysical properties. The structures formed in the presence of violaxanthin are characterized by minimized dissipation of excitation energy. In contrast, the structures formed in the presence of zeaxanthin show enhanced excitation quenching, thus protecting the system against photo-damage.

biophysics↗