Publication:
Extracellular Vesicles-Mediated Bio-Orthogonal Catalysis in Growing Tumors

dc.contributor.authorSancho-Albero, Maria
dc.contributor.authorSebastián, Víctor
dc.contributor.authorPerez-Lopez, Ana M
dc.contributor.authorMartin-Duque, Pilar
dc.contributor.authorUnciti-Broceta, Asier
dc.contributor.authorSantamaria, Jesus
dc.contributor.funderUnión Europea. Comisión Europea. European Research Council (ERC)
dc.contributor.funderAsociación Española Contra el Cáncer
dc.contributor.funderFundación Ramón Areces
dc.contributor.funderFundación BBVA
dc.contributor.funderEngineering and Physical Sciences Research Council (Reino Unido)
dc.date.accessioned2025-02-21T10:53:05Z
dc.date.available2025-02-21T10:53:05Z
dc.date.issued2024-04-16
dc.description.abstractSeveral studies have reported the successful use of bio-orthogonal catalyst nanoparticles (NPs) for cancer therapy. However, the delivery of the catalysts to the target tissues in vivo remains an unsolved challenge. The combination of catalytic NPs with extracellular vesicles (EVs) has been proposed as a promising approach to improve the delivery of therapeutic nanomaterials to the desired organs. In this study, we have developed a nanoscale bio-hybrid vector using a CO-mediated reduction at low temperature to generate ultrathin catalytic Pd nanosheets (PdNSs) as catalysts directly inside cancer-derived EVs. We have also compared their biodistribution with that of PEGylated PdNSs delivered by the EPR effect. Our results indicate that the accumulation of PdNSs in the tumour tissue was significantly higher when they were administered within the EVs compared to the PEGylated PdNSs. Conversely, the amount of Pd found in non-target organs (i.e., liver) was lowered. Once the Pd-based catalytic EVs were accumulated in the tumours, they enabled the activation of a paclitaxel prodrug demonstrating their ability to carry out bio-orthogonal uncaging chemistries in vivo for cancer therapy.
dc.description.peerreviewed
dc.description.sponsorshipThis research was funded by the ERC Advanced Grant CADENCE (ERC-2016-ADG-742684). MS-A thanks the AECC for postdoctoral research fellowship funding (POSTD234966SANC), “Ayuda a Talento AECC 2023”. VS acknowledges the funding from Fundación Ramón Areces (XX concurso nacional-ciencias de la vida y la materia) and beca Leonardo a Investigadores y creadores culturales 2021 de la Fundación BBVA. A.M.P.-L. and A.U.-B. thank EPSRC (EP/N021134/1) for funding.
dc.format.number8
dc.format.page691
dc.format.volume13
dc.identifier.citationSancho-Albero M, Sebastian V, Perez-Lopez AM, Martin-Duque P, Unciti-Broceta A, Santamaria J. Extracellular Vesicles-Mediated Bio-Orthogonal Catalysis in Growing Tumors. Cells. 2024 Apr 16;13(8):691.
dc.identifier.doi10.3390/cells13080691
dc.identifier.e-issn2073-4409
dc.identifier.journalCells
dc.identifier.pubmedID38667306
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26346
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/ERC-2016-ADG-742684
dc.relation.publisherversionhttps://doi.org/10.3390/cells13080691
dc.repisalud.centroISCIII::Centro Nacional de Microbiología (CNM)
dc.repisalud.institucionISCIII
dc.repisalud.instituteIIS::IIS Aragón - Instituto de Investigación Sanitaria Aragón (Aragón)
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBio-orthogonal catalysis
dc.subjectCancer
dc.subjectExtracellular vesicles
dc.subjectPalladium nanosheets
dc.subject.meshAnimals
dc.subject.meshCatalysis
dc.subject.meshCell Line, Tumor
dc.subject.meshExtracellular Vesicles
dc.subject.meshHumans
dc.subject.meshMice
dc.subject.meshMice, Nude
dc.subject.meshNanoparticles
dc.subject.meshNeoplasms
dc.subject.meshPaclitaxel
dc.subject.meshPalladium
dc.subject.meshPolyethylene Glycols
dc.subject.meshProdrugs
dc.subject.meshTissue Distribution
dc.titleExtracellular Vesicles-Mediated Bio-Orthogonal Catalysis in Growing Tumors
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication
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