Melittin Acts as a Radiosensitizer for Non-Small Cell Lung Cancer by Inhibiting the DNA Damage Repair System and...

This study aimed to evaluate the radiosensitizing effects of melittin, the main active component of bee venom, in non-small cell lung cancer (NSCLC) cells. Given the limitations of radiotherapy due to intrinsic tumor resistance, we investigated whether melittin could enhance the efficacy of radiation by promoting apoptosis and impairing DNA damage repair mechanisms.

NSCLC cell lines were treated with melittin and exposed to ionizing radiation. Clonogenic assays assessed radiosensitivity, while Western blot analyses examined DNA damage response proteins (DNA-PKcs, ATM, γ-H2AX) and apoptosis markers (Bax, cleaved caspase-3). In vivo, a BALB/c nude mouse xenograft model was used to evaluate the therapeutic effect of combined treatment. Tumor volume, weight, and immunohistochemical (IHC) staining were analyzed.

Melittin significantly enhanced radiosensitivity in NSCLC cells, as indicated by decreased colony formation. It reduced phosphorylation of DNA-PKcs and ATM while increasing γ-H2AX, suggesting impaired DNA double-strand break repair. Apoptotic activity increased with elevated Bax and cleaved caspase-3 levels. In vivo, combination therapy markedly inhibited tumor growth, as supported by IHC evidence of increased apoptosis and DNA damage.

Melittin is a potent radiosensitizer in NSCLC, impairing DNA repair and promoting apoptosis. These findings support its potential as a novel adjunct to radiotherapy to improve NSCLC treatment outcomes.