TY - JOUR
T1 - Artificial cell-derived vesicles by extrusion, a novel docetaxel drug delivery system for lung cancer
AU - Carrasco-Rojas, Javiera
AU - Zavala, Gabriela
AU - Contreras-Lopez, Rafael
AU - Olivares, Belén
AU - Aarsund, Miriam
AU - Inngjerdingen, Marit
AU - Nyman, Tuula A.
AU - Sandoval, Felipe I.
AU - Ramírez, Orlando
AU - Alarcón-Moyano, Jessica
AU - Díaz-Calderón, Paulo
AU - Jara-Sandoval, José Antonio
AU - Schuh, Christina M.A.P.
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/4
Y1 - 2025/4
N2 - Lung cancer (LC) has the highest mortality rate worldwide and novel therapies are being sought. Among those are cell-product-based therapies such as extracellular vesicles (EVs). Recently, it has been discovered that artificial cell-derived vesicle by extrusion (EXT) could be a potential tool to lower barriers to clinical translation. In this study we propose a formulation of human natural killer (NK) EXT encapsulating docetaxel (DTX) for LC therapy. EXT-DTXs were generated from NK cells by cell extrusion. EXTs and DTX-EXTs, were characterized and compared to EVs secreted by NK cells. All vesicles displayed a cup-shaped morphology with a mean size of <200 nm and stable composition, with zeta potentials between −26 and −33 mV. DTX-EXT contained 14 ± 9.1 p.m. DTX per μg of EXT protein. The proteome of EVs, EXT and DTX-EXT was analyzed and revealed a distinct protein enrichment pattern for each group. Uptake inhibition studies identified clathrin-mediated endocytosis as the primary internalization pathway for all vesicle types in A549 and H1975 LC cells. Cytotoxicity assays demonstrated that DTX-EXTs induced significantly higher apoptosis and reduced cell viability compared to EVs and EXTs, with higher efficacy in A549 cells. Notably, DTX-EXTs induced cytotoxic effects at picomolar docetaxel concentrations, 300–600 times lower than free DTX. This study provides the first comprehensive characterization of docetaxel-loaded NK artificially cell-derived vesicle by extrusion, highlighting their potential as a novel therapeutic delivery system with enhanced anti-tumor efficacy. Future studies are warranted to further explore the therapeutic potential and safety profile of DTX-EXTs in cancer treatment.
AB - Lung cancer (LC) has the highest mortality rate worldwide and novel therapies are being sought. Among those are cell-product-based therapies such as extracellular vesicles (EVs). Recently, it has been discovered that artificial cell-derived vesicle by extrusion (EXT) could be a potential tool to lower barriers to clinical translation. In this study we propose a formulation of human natural killer (NK) EXT encapsulating docetaxel (DTX) for LC therapy. EXT-DTXs were generated from NK cells by cell extrusion. EXTs and DTX-EXTs, were characterized and compared to EVs secreted by NK cells. All vesicles displayed a cup-shaped morphology with a mean size of <200 nm and stable composition, with zeta potentials between −26 and −33 mV. DTX-EXT contained 14 ± 9.1 p.m. DTX per μg of EXT protein. The proteome of EVs, EXT and DTX-EXT was analyzed and revealed a distinct protein enrichment pattern for each group. Uptake inhibition studies identified clathrin-mediated endocytosis as the primary internalization pathway for all vesicle types in A549 and H1975 LC cells. Cytotoxicity assays demonstrated that DTX-EXTs induced significantly higher apoptosis and reduced cell viability compared to EVs and EXTs, with higher efficacy in A549 cells. Notably, DTX-EXTs induced cytotoxic effects at picomolar docetaxel concentrations, 300–600 times lower than free DTX. This study provides the first comprehensive characterization of docetaxel-loaded NK artificially cell-derived vesicle by extrusion, highlighting their potential as a novel therapeutic delivery system with enhanced anti-tumor efficacy. Future studies are warranted to further explore the therapeutic potential and safety profile of DTX-EXTs in cancer treatment.
KW - Artificially cell-derived vesicles (ACDV)
KW - Cell extrusion
KW - Clathrin-dependent endocytosis
KW - Drug encapsulation
UR - http://www.scopus.com/inward/record.url?scp=85217418481&partnerID=8YFLogxK
U2 - 10.1016/j.jddst.2025.106693
DO - 10.1016/j.jddst.2025.106693
M3 - Article
AN - SCOPUS:85217418481
SN - 1773-2247
VL - 106
JO - Journal of Drug Delivery Science and Technology
JF - Journal of Drug Delivery Science and Technology
M1 - 106693
ER -