Journal of Siberian Federal University. Chemistry / Development of 3D Glioma Models Based on Cell Spheroids Embedded in Pectin- Collagen Matrix

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Supplementary material
Application 1 (.pdf, 210 KB)
Issue
Journal of Siberian Federal University. Chemistry. 2024 17 (4)
Authors
Lanskikh, Daria V.; Yakutovich, Dmitriy V.; Belousov, Andrei S.; Shved, Nikita A.; Kumeiko, Vadim V.
Contact information
Lanskikh, Daria V.: School of Medicine and Life Sciences, Far Eastern Federal University Vladivostok, Russian Federation; A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences Vladivostok, Russia Federation; Yakutovich, Dmitriy V. : School of Medicine and Life Sciences, Far Eastern Federal University Vladivostok, Russian Federation; Belousov, Andrei S.: School of Medicine and Life Sciences, Far Eastern Federal University Vladivostok, Russian Federation; Shved, Nikita A.: School of Medicine and Life Sciences, Far Eastern Federal University Vladivostok, Russian Federation; A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences Vladivostok, Russia Federation; Kumeiko, Vadim V. : School of Medicine and Life Sciences, Far Eastern Federal University Vladivostok, Russian Federation; A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch, Russian Academy of Sciences Vladivostok, Russia Federation;
Keywords
glioma; cell-based model; spheroids; biomaterials
Abstract

Three-dimensional cell culture is a modern tool for cancer research. This cell-based model combines the simplicity and accessibility of two-dimensional systems with mimicking in vivo conditions via supporting cell- cell and cell-matrix interactions. This allows it to be used both for studying the mechanisms of cancerogenesis and for preclinical testing anticancer therapeutics. In this research, we propose a simple and detailed technique for the preparation of spheroids composed of human glioblastoma cells embedded in a biopolymer matrix based on modified pectins supplemented with collagen I. The protocol also includes long-term cell monitoring with comprehensive analysis of cell viability, migration and behavior in culture using conventional optical imaging, laser scanning microscopy and flow cytometry

Pages
495–504
EDN
BNORRQ
Paper at repository of SibFU
https://elib.sfu-kras.ru/handle/2311/154317