Development of an Ex Vivo Functional Assay for Prediction of Irradiation Related Toxicity in Healthy Oral Mucosa Tissue

Author:

Pachler Katrin S.1,Lauwers Iris2,Verkaik Nicole S.1,Rovituso Marta3ORCID,van der Wal Ernst3,Mast Hetty4,Jonker Brend P.4ORCID,Sewnaik Aniel5,Hardillo Jose A.5ORCID,Keereweer Stijn5ORCID,Monserez Dominiek5ORCID,Kremer Bernd5,Koppes Sjors6,van den Bosch Thierry P. P.6ORCID,Verduijn Gerda M.2ORCID,Petit Steven2ORCID,Sørensen Brita S.278ORCID,van Gent Dik C.1ORCID,Capala Marta E.2

Affiliation:

1. Department of Molecular Genetics, Erasmus MC Cancer Institute, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands

2. Department of Radiotherapy, Erasmus MC Cancer Institute, 3015 GD Rotterdam, The Netherlands

3. Holland Proton Therapy Centre (HPTC), Huismansingel 4, 2629 JH Delft, The Netherlands

4. Department of Oral and Maxillofacial Surgery, Erasmus MC Cancer Institute, 3015 GD Rotterdam, The Netherlands

5. Department of Otorhinolaryngology and Head and Neck Surgery, Erasmus MC Cancer Institute, 3015 GD Rotterdam, The Netherlands

6. Department of Pathology, Erasmus MC Cancer Institute, 3015 GD Rotterdam, The Netherlands

7. Department of Experimental Clinical Oncology, Danish Centre for Particle Therapy, Aarhus University Hospital, 8200 Aarhus, Denmark

8. Department of Clinical Medicine, Aarhus University, Nordre Ringgade 1, 8000 Aarhus, Denmark

Abstract

Radiotherapy in the head-and-neck area is one of the main curative treatment options. However, this comes at the cost of varying levels of normal tissue toxicity, affecting up to 80% of patients. Mucositis can cause pain, weight loss and treatment delays, leading to worse outcomes and a decreased quality of life. Therefore, there is an urgent need for an approach to predicting normal mucosal responses in patients prior to treatment. We here describe an assay to detect irradiation responses in healthy oral mucosa tissue. Mucosa specimens from the oral cavity were obtained after surgical resection, cut into thin slices, irradiated and cultured for three days. Seven samples were irradiated with X-ray, and three additional samples were irradiated with both X-ray and protons. Healthy oral mucosa tissue slices maintained normal morphology and viability for three days. We measured a dose-dependent response to X-ray irradiation and compared X-ray and proton irradiation in the same mucosa sample using standardized automated image analysis. Furthermore, increased levels of inflammation-inducing factors—major drivers of mucositis development—could be detected after irradiation. This model can be utilized for investigating mechanistic aspects of mucositis development and can be developed into an assay to predict radiation-induced toxicity in normal mucosa.

Funder

HollandPTC-Varian consortium-confined call 2019

KWF Dutch Cancer Society

Publisher

MDPI AG

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