Research
Epitranscriptomics & Cancer Adaptation : A.David

Activities

Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

More..

Zotero public

Added by JPPOUGET
Group name EquipeJPP
Item Type Journal Article
Title Surface modification of extracellular vesicles with polyoxazolines to enhance their plasma stability and tumor accumulation
Creator Simon et al.
Author L. Simon
Author J. Constanzo
Author C. Terraza-Aguirre
Author Z. Ibn Elfekih
Author J. Berthelot
Author B. T. Benkhaled
Author T. Haute
Author K. Pednekar
Author K. Clark
Author S. J. Emerson
Author S. Atis
Author C. Benedetti
Author S. Langlois
Author A. Marquant
Author J. Prakash
Author A. Wang
Author J. M. Devoisselle
Author T. Montier
Author F. Djouad
Author J. P. Pouget
Author V. Lapinte
Author Marie Morille
Abstract Extracellular vesicles (EVs) are future promising therapeutics, but their instability in vivo after administration remains an important barrier to their further development. Many groups evaluated EV surface modification strategies to add a targeting group with the aim of controlling EV biodistribution. Conversely, fewer groups focused on their stabilization to obtain "stealth" allogenic EVs. Modulating their stabilization and biodistribution is an essential prerequisite for their development as nano-therapeutics. Here, we explored polyoxazolines with lipid anchors association to the EV membrane (POxylation as an alternative to PEGylation) to stabilize EVs in plasma and control their biodistribution, while preserving their native properties. We found that this modification maintained and seemed to potentiate the immunomodulatory properties of EVs derived from mesenchymal stem/stromal cells (MSC). Using a radiolabeling protocol to track EVs at a therapeutically relevant concentration in vivo, we demonstrated that POxylation is a promising option to stabilize EVs in plasma because it increased EV half-life by 6 fold at 6 h post-injection. Moreover, EV accumulation in tumors was higher after POxylation than after PEGylation.
Publication Biomaterials
Volume 313
Pages 122748
Date 2025-02
Journal Abbr Biomaterials
Language eng
DOI 10.1016/j.biomaterials.2024.122748
ISSN 1878-5905
Library Catalog PubMed
Extra PMID: 39180918
Tags biodistribution, Cell Line, Tumor, EV radiolabeling, Exosomes, Extracellular Vesicles, Female, Humans, Lipopolymer, Lipopolyoxazoline, Mesenchymal Stem Cells, Mice, Mice, Inbred C57BL, original, Oxazoles, Post-insertion, Surface Properties, Tissue Distribution
Date Added 2024/12/07 - 07:04:05
Date Modified 2025/01/10 - 13:04:29
Notes and Attachments PubMed entry (Attachment)


© Institut de Recherche en Cancérologie de Montpellier - 2011 - Tous droits réservés - Mentions légales - Connexion - Conception : ID Alizés