Radiation-induced and obesity-dependent NK cell activities
Radiation-induced and obesity-dependent NK cell activities
Disciplines
Clinical Medicine (30%); Medical-Theoretical Sciences, Pharmacy (70%)
Keywords
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Breast cancer,
Metastasis,
Radiotherapy,
Obesity,
NK cells
Radiation therapy (RT) is one of the leading therapeutic approaches used in the management of metastatic breast cancer (BC). However, currently existing RT schedules are limited in their efficacy due to the impossibility to reach a curative radiation dose for killing of aggressive and radiation resistant carcinoma cells. Although high -LET irradiation could more efficiently eradicate therapy resistant carcinoma cells in comparison with photon -based RT, it is unclear whether it could also better mobilize immune cells for elimination of undifferentiated and radioresistant cancer stem cells (CSCs). Currently, overweight and obesity is an increasing problem that can diminish an efficacy of RT and alter immune response in patients with metastatic BC. Unfortunately, it is still unknown how adipocytes can contribute to the crosstalk between carcinoma and immune cells upon low- and high-LET radiation exposure. Research objectives: elucidation of the role of obese microenvironment in the regulation of cytotoxic activities of low- and high-LET ionizing radiations and NK cells against BC cells with enhanced metastatic properties.
- Slavisa Tubin, EBG Medaustron GmbH , national collaboration partner
- Christian Ploner, Medizinische Universität Innsbruck , national collaboration partner
- Sergej Skvortsov, Medizinische Universität Innsbruck , national collaboration partner
- Alessandra Bisio, Università di Trento - Italy
- Yari Ciribilli, Università di Trento - Italy
- Monica Marchese, Luxembourg Institute of Health - Luxembourg
- Olga Kofanova, Luxembourg Institute of Health - Luxembourg
- Maja Cemazar, Institute of Oncology Ljubljana - Slovenia
- Anahid Jewett, UCLA School of Dentistry - USA
Research Output
- 14 Citations
- 1 Publications
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2023
Title Erk1/2-Dependent HNSCC Cell Susceptibility to Erastin-Induced Ferroptosis DOI 10.3390/cells12020336 Type Journal Article Author Savic D Journal Cells Pages 336 Link Publication