hyaluronic acid-modified liposomes for ursolic acid-targeted delivery treat lung cancer based on p53/arts-mediated mitochondrial apoptosis

Background: chemotherapy drugs can cause drug resistance and other problems when treating lung cancer, which leads to treatment failure. ursolic acid (ua) is used in formulations based on traditional chinese medicine. ua has excellent anti-tumor effects, but they are limited by solubility and non-specificity to tumor cells.objectives: to overcome these issues, we created a novel hyaluronic acid (ha)-targeted liposome system for delivering ua (ha-lipo/ua) to explore the targeting and anti-tumor effects of ua.methods: we constructed the ha-lipo/ua delivery system by the thin film hydration method. the uptake and localization of ua were detected by flow cytometry and microscope. cell proliferation of a549 cells was detected by mtt assays. apoptosis and reactive oxygen species (ros) expression of a549 cells were also evaluated after being treated with ha-lipo/ua. western blot analysis evaluated the anti-tumor mechanism of ha-lipo/ua. results: ha-lipo/ua exhibited favorable targeting of the cluster of differentiation (cd)44-overexpressing a549 cells. ha-lipo/ua exhibited significant inhibition of the proliferation of a549 cells and induced their apoptosis compared with the corresponding monotherapies. ha-lipo/ua induced overexpression of reactive oxygen species and upregulated expression of p53 and apoptosis-related protein in the transforming growth factor-β signaling (arts) pathway, which induced cytochrome-c release, activation of caspase-3, and promoted mitochondrial apoptosis in a549 cells.conclusions: taken together, these data suggested that ha-lipo/ua could be used to target tumor cells.