Cargo-eliminated osteosarcoma-derived small extracellular vesicles mediating competitive cellular uptake for inhibiting pulmonary metastasis of osteosarcoma

Bibliographic Details
Title: Cargo-eliminated osteosarcoma-derived small extracellular vesicles mediating competitive cellular uptake for inhibiting pulmonary metastasis of osteosarcoma
Authors: Shanyi Lin, Longqiang Shu, Yuhang Guo, Ji Yuan, Juntao Zhang, Yang Wang, Yunlong Yang, Ting Yuan
Source: Journal of Nanobiotechnology, Vol 22, Iss 1, Pp 1-17 (2024)
Publisher Information: BMC, 2024.
Publication Year: 2024
Collection: LCC:Biotechnology
LCC:Medical technology
Subject Terms: Tumor derived small extracellular vesicles, Osteosarcoma, Cargo elimination, Lung fibroblast, Pre-metastatic niche, Biotechnology, TP248.13-248.65, Medical technology, R855-855.5
More Details: Abstract Osteosarcoma (OS) derived small extracellular vesicles (OS-sEVs) have been shown to induce the formation of cancer-associated fibroblasts (CAFs), characterized by elevated pro-inflammatory factor expression and enhanced migratory and contractile abilities. These CAFs play a crucial role in priming lung metastasis by orchestrating the pre-metastatic niche (PMN) in the lung. Disrupting the communication between OS-sEVs and lung fibroblasts (LFs) emerges as a potent strategy to hinder OS pulmonary metastasis. Our previously established saponin-mediated cargo-elimination strategy effectively reduces the cancer-promoting ability of tumor-derived small extracellular vesicles (TsEVs) while preserving their inherent targeting capability. In this study, we observed that cargo-eliminated OS-sEVs (CE-sEVs) display minimal pro-tumoral and LFs activation potential, yet retain their ability to target LFs. The uptake of OS-sEVs by LFs can be concentration-dependently suppressed by CE-sEVs, preventing the conversion of LFs into CAFs and thus inhibiting PMN formation and pulmonary metastasis of OS. In summary, this study proposes a potential strategy to prevent LFs activation, PMN formation in the lung, and OS pulmonary metastasis through competitive inhibition of OS-sEVs’ function by CE-sEVs.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1477-3155
Relation: https://doaj.org/toc/1477-3155
DOI: 10.1186/s12951-024-02636-9
Access URL: https://doaj.org/article/933ab30648ef42a69c0087bb163eb04e
Accession Number: edsdoj.933ab30648ef42a69c0087bb163eb04e
Database: Directory of Open Access Journals
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More Details
ISSN:14773155
DOI:10.1186/s12951-024-02636-9
Published in:Journal of Nanobiotechnology
Language:English