Abstract
Background: Ovarian cancer typically presents at an advanced stage, has a poor prognosis, and is a leading cause of cancer-related deaths in women. Extracellular vesicles (EVs) are cell membrane-derived nanoparticles that function in specific cell- to-cell communication and are under development as novel drug delivery vehicles and modulators of the tumor microenvironment. Artificial cell-derived vesicles (ACDVs) from M1 macrophages are able to repolarize macrophages from a M2 to a M1 phenotype and target tumor cells in in vitro studies.
Results: In this study, we generated engineered EVs (EEVs) by membrane disruption of M1 macrophages (MEVs) with and without cisplatin to generate cisplatin-loaded MEVs (C-MEVs) and empty MEVs (E-MEVs), which we tested in an ovarian cancer mouse xenograft model. E-MEVs and C-MEVs exhibited significantly less weight loss and equivalent activity to cisplatin, with improved activity over controls.
Conclusions: Further development of MEVs for the treatment of ovarian cancer is warranted.
Document Type
Article
Publication Date
2025
Digital Object Identifier (DOI)
https://doi.org/10.1186/s12645-025-00337-y
Funding Information
Research supported by NCI T32 CA160003, Kentucky Network for Innovation & Commercial Grant 30481152221.
Repository Citation
Cao, Connie D.; McCorkle, J. Robert; Allison, Derek B.; Yan, Donglin; Hill, Kristen S.; Li, Lan; Jayswal, Rani; Schweer, David; Dietrich, Charles S. III; Ueland, Frederick R.; Richards, Christopher I.; and Kolesar, Jill M., "M1 macrophage‑engineered vesicles have anti‑cancer activity in ovarian cancer" (2025). Markey Cancer Center Faculty Publications. 439.
https://uknowledge.uky.edu/markey_facpub/439

Notes/Citation Information
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