Shi-Yi Tian, Ming-Qing Peng, Min Li
Propofol is widely used in anesthesia, but its role in breast cancer progression remains controversial. This study investigated the molecular mechanisms of propofol in breast cancer, focusing on IL-6 and tumor microenvironment modulation. Bioinformatics analysis identified IL-6 as a potential target of propofol. MCF-7 cells were treated with varying propofol concentrations (0–100 ?g/mL), and cell viability was assessed via CCK-8 assay. Propofol at 50 ?g/mL significantly reduced viability, while 25 ?g/mL (a non-cytotoxic dose) was selected for further experiments. Western blot confirmed propofol down regulated IL-6 expression. Functional assays demonstrated that propofol suppressed migration, invasion, and angiogenesis in MCF-7 cells; and effects that were reversed by recombinant human IL-6 (rhIL-6). Molecular docking analysis further supported the interaction between propofol and IL-6. Additionally, IL-6 and VEGF-C were found to be co-expressed, suggesting a possible link between propofol and vascular mimicry inhibition. These findings indicate that propofol may exert anti-tumor effects in breast cancer by targeting IL-6, thereby inhibiting key oncogenic processes. This study provides new insights into the potential therapeutic benefits of propofol in breast cancer management.
Breast neoplasms
propofol
neoangiogenesis
cell migration
interleukin-6