2022
DOI: 10.21037/atm-21-4138
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Engineered exosomes for targeted delivery of miR-187-3p suppress the viability of hemangioma stem cells by targeting Notch signaling

Abstract: Contributions: (I) Conception and design: JW Zheng; (II) Administrative support: JW Zheng; (III) Provision of study materials or patients: ZL Zhao;

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Cited by 4 publications
(1 citation statement)
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“…After internalization, E-exos suppressed the Notch signaling pathway through the inhibition of miR-187-3p, thereby inhibiting the proliferation of HemSCs and providing a new research avenue for the treatment of IHs. 46 In the same year, based on the specific binding interaction between integrin α4β1 on the cell membrane of macrophages and vascular cell adhesion molecule-1 (VCAM-1), which is highly expressed on endothelial cells, 90 researchers co-incubated rapamycin with macrophage-derived exosomes and used extrusion to prepare drug-loaded particles (RNs). These particles were then encapsulated with PLGA microspheres to obtain rapamycin-encapsulated exosome-mimetic nanoparticles-in-PLGA microspheres (RNM).…”
Section: Targeting Strategy and Application Of Targeted Agents In Ihsmentioning
confidence: 99%
“…After internalization, E-exos suppressed the Notch signaling pathway through the inhibition of miR-187-3p, thereby inhibiting the proliferation of HemSCs and providing a new research avenue for the treatment of IHs. 46 In the same year, based on the specific binding interaction between integrin α4β1 on the cell membrane of macrophages and vascular cell adhesion molecule-1 (VCAM-1), which is highly expressed on endothelial cells, 90 researchers co-incubated rapamycin with macrophage-derived exosomes and used extrusion to prepare drug-loaded particles (RNs). These particles were then encapsulated with PLGA microspheres to obtain rapamycin-encapsulated exosome-mimetic nanoparticles-in-PLGA microspheres (RNM).…”
Section: Targeting Strategy and Application Of Targeted Agents In Ihsmentioning
confidence: 99%