Optimisation of conditions for the formation of spheroids of head and neck squamous cell carcinoma cell lines for use as animal alternatives

• Verfasst von: Tenschert, Esther [VerfasserIn]
• Verfasst von: Kern, Johann [VerfasserIn]
• Verfasst von: Affolter, Annette [VerfasserIn]
• Verfasst von: Rotter, Nicole [VerfasserIn]
• Verfasst von: Lammert, Anne [VerfasserIn]
• Titel: Optimisation of conditions for the formation of spheroids of head and neck squamous cell carcinoma cell lines for use as animal alternatives
• Verf.angabe: Esther Tenschert, Johann Kern, Annette Affolter, Nicole Rotter, and Anne Lammert
• E-Jahr: 2022
• Jahr: November 2022
• Umfang: 9 S.
• Fussnoten: Gesehen am 13.03.2023
• Titel Quelle: Enthalten in: Alternatives to laboratory animals
• Ort Quelle: London : SAGE Publications Ltd, 1981
• Jahr Quelle: 2022
• Band/Heft Quelle: 50(2022), 6 vom: Nov., Seite 414-422
• ISSN Quelle: 2632-3559
• DOI: doi:10.1177/02611929221135042
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: cancer
• Sach-SW: cancer cells
• Sach-SW: cell lines
• Sach-SW: coculture
• Sach-SW: culture models
• Sach-SW: drug discovery
• Sach-SW: heterogeneity
• Sach-SW: in vitro
• Sach-SW: microenvironment
• Sach-SW: spheroid
• Sach-SW: HNSCC
• K10plus-PPN: 1839065265

Abstract

The use of in vitro 3-D cell culture models in cancer research has yielded substantial gains in knowledge on various aspects of tumour biology. Such cell culture models could be useful in the study of head and neck squamous cell carcinoma (HNSCC), where mimicking intratumoral and intertumoral heterogeneity is especially challenging. Our research aims to establish 3-D spheroid models for HNSCC that reproduce in vitro the connections between tumour cells and the surrounding microenvironment. The aims of this study were to determine the optimal conditions for the culture and use of spheroids from HNSCC cell lines and optimal timepoint for using the spheroids obtained, to evaluate the effects of coculture with tumour-specific fibroblasts on spheroid formation, and to investigate spheroid responses to cisplatin treatment. Four HNSCC cell lines (UMSCC-11A, UMSCC-11B, UMSCC-22B and UD-SCC-01) were seeded in flat or round bottom well ultra-low attachment spheroid plates, and spheroid formation was evaluated. The HNSCC cell lines were then cocultured with stromal cells of the tumour microenvironment, producing an accelerated formation of dense spheroids. The viability of cells within the spheroids was assessed during cell culture by using a fluorescent dye. Our results suggest that: three out of the four cell lines tested could form usable spheroids with acceptable viability; the addition of stromal cells did not improve the number of viable cells; and the use of round bottom well plates supported the formation of a single spheroid, whereas flat bottom well plates led to the formation of multiple spheroids of different sizes.