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Organ-Specific Uptake of Extracellular Vesicles Secreted by Urological Cancer Cells. | LitMetric

AI Article Synopsis

  • Extracellular vesicles (EVs) from cancer cells significantly contribute to tumor development by creating supportive environments and preparing distant sites for metastasis.
  • This study investigated how different organs absorb EVs from benign and malignant urological cancer cells using a specific experimental method with immunodeficient mice.
  • The findings revealed that malignant cell-derived EVs are taken up more efficiently than those from benign cells, with absorption varying by organ, indicating a potential link between EVs and cancer metastasis that needs further research.

Article Abstract

Extracellular vesicles (EVs) secreted by cancer cells have been shown to take a pivotal part in the process of local and systemic tumor progression by promoting the formation of a supportive local tumor microenvironment and preparing premetastatic niches in distant organ systems. In this study, we analyzed the organ-specific uptake of EVs secreted by urological cancer cells using an innovative in-vivo approach. EVs from benign and malignant prostate, kidney, and bladder cells were isolated using ultracentrifugation, fluorescence-labeled and injected intravenously in immunodeficient mice. After 12 or 24 h, the animals were sacrificed, their organs were harvested and analyzed for the presence of EVs by high-resolution fluorescence microscopy. Across all entities, EVs were taken up fast (12 h > 24 h), and EVs from malignant cells were taken up more efficiently than EVs from benign cells. Though not entirely organ-specific, EVs were incorporated in different amounts, depending on the entity (prostate: lung > liver > brain; kidney: brain > lung > liver; bladder: lung > liver > brain). EV uptake in other organs than lung, liver, brain, and spleen was not observed. Our results suggest a role of EVs in the formation of premetastatic niches and an organotropism in EV uptake, which have to be examined in more detail in further studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508228PMC
http://dx.doi.org/10.3390/cancers13194937DOI Listing

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