Abstract
This study investigated the anti-PD-1/PD-L1 inhibition potential of the flavonoid cosmosiin against breast cancer (BC) using computational chemistry, network pharmacology, bioinformatics, and validated by experimental assays. Execution of Density Functional Theory (DFT) calculations was achieved by GAUSSIAN 09 with the 6-311G/B3LYP formalism to assess cosmosiin's physicochemical properties. Potential targets of cosmosiin were identified through SuperPred, Stitch, and SwissTargetPrediction databases, while BC-allied targets were sourced by accessing GeneCards. Overlapping analysis using Venny 2.0 identified 25 common targets between 38 targets of cosmosiin and 1314 targets of breast cancer. CytoHubba analysis highlighted 10 hub genes, with PTGS2, NFKB1, and CDK5 being the most significant. Molecular docking revealed stable binding of cosmosiin to CDK5 (-8.5 kcal mol(-1)), NFKB1 (-7.6 kcal mol(-1)), and PTGS2 (-9.6 kcal mol(-1)), confirmed by molecular dynamics simulations. GEPIA analysis linked the expression of these genes to survival outcomes and disease stage in breast cancer. Experimentally, cosmosiin was tested on MCF-7 (breast cancer) and MCF-10 (non-tumorigenic) cells. Cytotoxicity was evaluated using the MTT assay, showing dose-dependent viability reduction in MCF-7 cells with minimal impact on MCF-10 cells, thus exhibiting selective cytotoxicity. Phase-contrast microscopy revealed altered morphology in treated MCF-7 cells. Annexin V/PI flow cytometry confirmed increased early and late apoptosis, while EdU incorporation assays indicated decreased DNA synthesis and reduced proliferation. Transwell assays demonstrated up to 81% inhibition of cell migration at higher concentrations. Western blotting validated downregulation of CDK5, NFKB1, and PTGS2, aligning with computational predictions. These findings highlight selective, multi-targeted anticancer activity of cosmosiin, particularly through PTGS2, NFKB1, and CDK5, supporting its therapeutic potency for breast cancer with favorable effects on apoptosis, proliferation, and cell migration, while correlating with survival and immune infiltration outcomes.