GR: Oncosuppressor in KRAS driven lung cancer
GR: Oncosuppressor in KRAS driven lung cancer
Disciplines
Biology (40%); Medical-Theoretical Sciences, Pharmacy (60%)
Keywords
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Glucocorticoid Receptor,
Lung Cancer,
KRAS,
Tumor Microenvironment,
Genetically Engineered Mouse Model
Lung cancer is a devastating disease and is the leading cause of most tumor-associated deaths. At the genetic level, lung tumors are classified based on different mutations, and specific genetic changes determine the chosen treatment methods for affected patients. The most commonly mutated gene in lung cancer is KRAS, and there is still no well-established targeted treatment method for this gene. The majority of affected patients receive a type of immunotherapy, where efforts are made to support the body`s own immune cells in fighting the tumor. However, various factors can significantly influence the success of such therapy. Additionally, many patients are prescribed synthetic glucocorticoids for symptom management, which are structurally derived from a natural stress hormone, cortisol. Interestingly, relatively little is known about the direct effects of these hormones on lung cancer cells and thus the impact of different treatment methods. The aim of this project is to close this gap and thereby achieve improvements in the care of lung cancer patients.
- Judit Moldvay, Semmelweis University - Hungary
Research Output
- 1 Citations
- 1 Publications
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2025
Title Loss of SPHK1 fuels inflammation to drive KRAS-mutated lung adenocarcinoma DOI 10.1016/j.canlet.2025.217733 Type Journal Article Author Luca A Journal Cancer Letters Pages 217733 Link Publication