4.7 Article

Human Mesenchymal Stromal Cells Do Not Cause Radioprotection of Head-and-Neck Squamous Cell Carcinoma

Journal

Publisher

MDPI
DOI: 10.3390/ijms23147689

Keywords

mesenchymal stromal cells; head-and-neck squamous cell carcinoma; head-and-neck cancer; radiotherapy; radiosensitivity; radioresistance; co-culture

Funding

  1. IMM-PACT-Programme for Clinician Scientists, Department of Medicine II, Medical Center-University of Freiburg
  2. Faculty of Medicine, University of Freiburg - Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [413517907]
  3. MOTI-VATE scholarship of the Faculty of Medicine, University of Freiburg
  4. German Red Cross Blood Service Baden-Wurttemberg-Hessen, Mannheim, Germany
  5. Wissenschaftliche Gesellschaft Freiburg

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This study investigated the influence of mesenchymal stromal cells (MSCs) on the radiosensitivity of head-and-neck squamous cell carcinoma (HNSCC). The results showed that MSCs did not exert radioprotective effects on HNSCCs and can be safely used for radiotherapy-related issues in HNSCC patients.
Radiotherapy of head-and-neck squamous cell carcinoma (HNSCC) can cause considerable normal tissue injuries, and mesenchymal stromal cells (MSCs) have been shown to aid regeneration of irradiation-damaged normal tissues. However, utilization of MSC-based treatments for HNSCC patients undergoing radiotherapy is hampered by concerns regarding potential radioprotective effects. We therefore investigated the influence of MSCs on the radiosensitivity of HNSCCs. Several human papillomavirus (HPV)-negative and HPV-positive HNSCCs were co-cultured with human bone marrow-derived MSCs using two-dimensional and three-dimensional assays. Clonogenic survival, proliferation, and viability of HNSCCs after radiotherapy were assessed depending on MSC co-culture. Flow cytometry analyses were conducted to examine the influence of MSCs on irradiation-induced cell cycle distribution and apoptosis induction in HNSCCs. Immunofluorescence stainings of gamma H2AX were conducted to determine the levels of residual irradiation-induced DNA double-strand breaks. Levels of connective tissue growth factor (CTGF), a multifunctional pro-tumorigenic cytokine, were analyzed using enzyme-linked immunosorbent assays. Neither direct MSC co-culture nor MSC-conditioned medium exerted radioprotective effects on HNSCCs as determined by clonogenic survival, proliferation, and viability assays. Consistently, three-dimensional microwell arrays revealed no radioprotective effects of MSCs. Irradiation resulted in a G2/M arrest of HNSCCs at 96 h independently of MSC co-culture. HNSCCs' apoptosis rates were increased by irradiation irrespective of MSCs. Numbers of residual gamma H2AX foci after irradiation with 2 or 8 Gy were comparable between mono- and co-cultures. MSC mono-cultures and HNSCC-MSC co-cultures exhibited comparable CTGF levels. We did not detect radioprotective effects of human MSCs on HNSCCs. Our results suggest that the usage of MSC-based therapies for radiotherapy-related toxicities in HNSCC patients may be safe in the context of absent radioprotection.

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