Proton Compared to X-Irradiation Induces Different Protein Profiles in Oral Cancer Cells and Their Derived Extracellular Vesicles

Author:

Juvkam Inga Solgård12ORCID,Zlygosteva Olga3ORCID,Sitarz Mateusz4,Thiede Bernd5ORCID,Sørensen Brita Singers46,Malinen Eirik23ORCID,Edin Nina Jeppesen3ORCID,Søland Tine Merete17,Galtung Hilde Kanli1

Affiliation:

1. Institute of Oral Biology, Faculty of Dentistry, University of Oslo, 0372 Oslo, Norway

2. Department of Radiation Biology, Institute for Cancer Research, Oslo University Hospital, 0379 Oslo, Norway

3. Department of Physics, Faculty of Mathematics and Natural Sciences, University of Oslo, 0371 Oslo, Norway

4. Danish Centre for Particle Therapy, Aarhus University Hospital, 8200 Aarhus, Denmark

5. Department of Biosciences, Faculty of Mathematics and Natural Sciences, University of Oslo, 0371 Oslo, Norway

6. Department of Experimental Clinical Oncology, Aarhus University Hospital, 8200 Aarhus, Denmark

7. Department of Pathology, Oslo University Hospital, 0372 Oslo, Norway

Abstract

Extracellular vesicles (EVs) are membrane-bound particles released from cells, and their cargo can alter the function of recipient cells. EVs from X-irradiated cells have been shown to play a likely role in non-targeted effects. However, EVs derived from proton irradiated cells have not yet been studied. We aimed to investigate the proteome of EVs and their cell of origin after proton or X-irradiation. The EVs were derived from a human oral squamous cell carcinoma (OSCC) cell line exposed to 0, 4, or 8 Gy from either protons or X-rays. The EVs and irradiated OSCC cells underwent liquid chromatography–mass spectrometry for protein identification. Interestingly, we found different protein profiles both in the EVs and in the OSCC cells after proton irradiation compared to X-irradiation. In the EVs, we found that protons cause a downregulation of proteins involved in cell growth and DNA damage response compared to X-rays. In the OSCC cells, proton and X-irradiation induced dissimilar cell death pathways and distinct DNA damage repair systems. These results are of potential importance for understanding how non-targeted effects in normal tissue can be limited and for future implementation of proton therapy in the clinic.

Funder

UiO Life Science at the University of Oslo

Southern-Eastern Norway Regional Health Authority

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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