ArticleCancer management and research2026
Hyperbaric Oxygen Reverses High-Glucose-Induced Stemness and Radioresistance in Non-Small Cell Lung Cancer Cells.
Article in Cancer management and research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Hyperglycemia may promote aggressive phenotypes and treatment resistance in non-small cell lung cancer (NSCLC). We investigated whether chronic high glucose (HG) exposure induces stem cell-like properties and radioresistance and whether hyperbaric oxygen (HBO) reverses these effects. Methods: H1299 and A549 cells were maintained under normal glucose (NG; 5.5 mM D-glucose) or high glucose (HG; 25 mM D-glucose) conditions. Acute effects were evaluated by switching NG-grown cells to NG or HG and performing MTT assays. For all other experiments, cells were conditioned in HG for 3 months. Protein expression of glucose transporter-1 (Glut1), hypoxia-inducible factor-1α (HIF-1α), CD133, SOX2, and OCT4 was assessed by immunoblotting. Stem-like behavior and radiosensitivity were evaluated by tumorsphere formation and clonogenic survival assays following irradiation. HBO (100% O Results: Acute HG increased cell viability, whereas long-term HG conditioning did not significantly alter short-term viability but increased tumorsphere formation and clonogenic survival after irradiation. HG upregulated Glut1 and HIF-1α and increased SOX2 and OCT4 expression. Additional analyses showed that 4 weeks, but not 1 week, of continuous HBO exposure reduced HIF-1α, SOX2, and OCT4 expression under HG conditions, whereas Glut1 expression was not markedly altered. HBO suppressed HG-enhanced tumorsphere formation and reversed HG-associated radioresistance. Conclusion: Chronic HG promoted stem-like and radioresistant phenotypes in NSCLC cells. Prolonged HBO exposure for 4 weeks attenuated these effects and was associated with reduced HIF-1α, SOX2, and OCT4 expression, supporting HBO as a potential preclinical adjunct strategy for mitigating HG-associated therapeutic resistance.
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