In a study (https://doi.org/10.1016/j.bioana.2024.05.002) published in the KeAi journal Biomedical Analysis, a group of researchers from China outline a new discrimination and treatment approach — a novel exosome-based drug delivery system that could improve the cell entry ability of drugs and the targeting of cancer cells. This approach provides a new drug delivery system and synergistic therapy idea, paving the way for future clinical applications.
“Exosomes are extracellular vesicles with lipid bilayers that have been extensively used as delivery vehicles for multiple drugs due to their high biocompatibility, low immunogenicity, the abilities to cross various biological barriers and evade the clearance by immune system,” explains the study’s corresponding author Songqin Liu, a professor at the Jiangsu Engineering Laboratory of Smart Carbon-Rich Materials and Device at Southeast University. “The synergistic cancer treatment by loading various nucleic acids and drugs into exosomes utilizes the advantages of different therapeutic approaches and has been applied to effectively treat cancers through the synergy of different treatment mechanisms.”
Autophagy is an intracellular degradative process where a cell engulfs its own cytoplasmic proteins or organelles and encapsulates them into autophagosomes. Many studies have shown that in cancer biology, autophagy plays a dual role in tumor promotion and inhibition. Notably, inhibition of autophagy shows potential in improving the clinical treatment of cancer patients.
“We constructed a novel antitumor exosome-based drug delivery system employing the synergistic effects of miRNA-regulated autophagy inhibition and coumarin anticancer drugs to achieve effective treatment of ovarian cancer,” says Xin Hua, first author of the study. “With the anti-tumor effects and intracellular visualization from 7-coumarin, the regulation of the autophagy process from encapsulated miRNA, the targeting of cancer cells from exosome, the synergistic effect and exosome-based drug delivery strategy for anti-cancer therapy showed promising prospects for in vitro and clinical applications.”
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References
DOI
Original Source URL
https://doi.org/10.1016/j.bioana.2024.05.002
Funding information
This project was supported by the ZhiShan Scholar Program of Southeast University (2242022R40053).
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