# Two-color spheroid model for determining the O2-induced radiosensitivity of HNSCC

**Authors:** Danny Knobloch-Sperlich, Matthias Kappler, Markus Glaß, Antje Güttler, Marina Petrenko, Jonas Pyko, Tony Gutschner, Frank Tavasol, Dirk Vordermark, Matthias Bache

PMC · DOI: 10.1186/s13036-025-00611-y · Journal of Biological Engineering · 2026-01-08

## TL;DR

A two-color spheroid model was developed to study how oxygen levels affect the radiosensitivity of head and neck cancer cells.

## Contribution

A novel two-color spheroid model with fluorescently labeled cell layers was created to study hypoxia-induced radiosensitivity in HNSCC.

## Key findings

- The inner GFP-labeled cells showed lower plating efficiency and increased radiation resistance, similar to 2D hypoxic cells.
- Adding ascorbic acid reduced normoxia-induced HIF1α expression and increased spheroid growth and radioresistance under normoxia.
- The model provides a robust method to distinguish hypoxic from normoxic tumor areas in radiotherapy research.

## Abstract

Hypoxia strongly affects the growth, invasion, and therapeutic response of solid tumors, including head and neck squamous cell carcinoma (HNSCC). Despite intensive research, only a few substances have progressed to clinical trials as radiosensitizers. Therefore, new clinically relevant tumor models are needed to identify agents that overcome radiation resistance in hypoxic tumors. To study radiosensitivity of hypoxic and normoxic cells, we developed a two-color spheroid model using two HNSCC cell lines, SAS and FaDu, with GFP-labeled inner cell layers and mCherry-labeled outer layers. Optimizing the ratios of fluorescent cells enabled formation of hypoxic and normoxic zones, confirmed by pimonidazole, HIF1α, and CA IX staining. A newly established fluorescence clonogenic survival assay demonstrated transferability of results from 2D normoxia and hypoxia assays to these 3D model. The inner GFP-labeled cells showed significantly lower plating efficiency and increased radiation resistance compared to outer mCherry-labeled cells, similar to 2D hypoxic cells. To improve the model by reducing normoxia-induced HIF1α expression in the outer layer, we added physiological concentrations of ascorbic acid. Ascorbic acid also increased spheroid growth, clonogenic survival, and radioresistance under normoxia, while hypoxic responses remained unchanged. These two-layer spheroid model with distinct fluorescent labels provide a simple, robust assay to distinguish hypoxic from normoxic tumor areas in radiotherapy research. Addition of ascorbic acid further refines the physiological relevance of 3D tumor models and modulates radiosensitivity of the outer mCherry-labeled cell layer in both HNSCC models.

The online version contains supplementary material available at 10.1186/s13036-025-00611-y.

## Linked entities

- **Proteins:** HIF1A (hypoxia inducible factor 1 subunit alpha), CA9 (carbonic anhydrase 9)
- **Chemicals:** ascorbic acid (PubChem CID 9888239), pimonidazole (PubChem CID 50981)
- **Diseases:** head and neck squamous cell carcinoma (MONDO:0010150), HNSCC (MONDO:0010150)

## Full-text entities

- **Diseases:** HNSCC (MESH:D000077195)
- **Chemicals:** O2 (-)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12836854/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12836854/full.md

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Source: https://tomesphere.com/paper/PMC12836854