Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/108282
DC FieldValueLanguage
dc.contributor.authorBoto, Carlos-
dc.contributor.authorQuartin, Emanuel-
dc.contributor.authorCai, Yijun-
dc.contributor.authorMartín-Lorenzo, Alberto-
dc.contributor.authorCenador, María Begoña García-
dc.contributor.authorPinto, Sandra-
dc.contributor.authorGupta, Rajeev-
dc.contributor.authorEnver, Tariq-
dc.contributor.authorSánchez-García, Isidro-
dc.contributor.authorHong, Dengli-
dc.contributor.authorNeves, Ricardo Pires das-
dc.contributor.authorFerreira, Lino-
dc.date.accessioned2023-08-22T11:07:24Z-
dc.date.available2023-08-22T11:07:24Z-
dc.date.issued2017-05-11-
dc.identifier.issn2041-1723pt
dc.identifier.urihttps://hdl.handle.net/10316/108282-
dc.description.abstractLeukaemia cells that are resistant to conventional therapies are thought to reside in protective niches. Here, we describe light-inducible polymeric retinoic acid (RA)-containing nanoparticles (NPs) with the capacity to accumulate in the cytoplasm of leukaemia cells for several days and release their RA payloads within a few minutes upon exposure to blue/UV light. Compared to NPs that are not activated by light exposure, these NPs more efficiently reduce the clonogenicity of bone marrow cancer cells from patients with acute myeloid leukaemia (AML) and induce the differentiation of RA-low sensitive leukaemia cells. Importantly, we show that leukaemia cells transfected with light-inducible NPs containing RA can engraft into bone marrow in vivo in the proximity of other leukaemic cells, differentiate upon exposure to blue light and release paracrine factors that modulate nearby cells. The NPs described here offer a promising strategy for controlling distant cell populations and remotely modulating leukaemic niches.pt
dc.language.isoengpt
dc.publisherSpringer Naturept
dc.relationPTDC/CTM-NAN/120552/2010pt
dc.relationUID/NEU/04539/2013pt
dc.relationSFRH/BD/62419/2009pt
dc.relationSFRH/BD/90964/2012pt
dc.relationPOCI-01- 0145-FEDER-016390:CANCEL STEMpt
dc.relationERC project n 307384, ‘Nanotriggerpt
dc.relationMINECO (SAF2012-32810, SAF2015-64420-R and Red de Excelencia Consolider OncoBIO SAF2014-57791-REDCpt
dc.relationBloodwise and CRUK programme grantspt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshAgedpt
dc.subject.meshAged, 80 and overpt
dc.subject.meshAnimalspt
dc.subject.meshBenzene Derivativespt
dc.subject.meshCell Line, Tumorpt
dc.subject.meshDrug Compoundingpt
dc.subject.meshFemalept
dc.subject.meshFormatespt
dc.subject.meshHuman Umbilical Vein Endothelial Cellspt
dc.subject.meshHumanspt
dc.subject.meshLeukemia, Promyelocytic, Acutept
dc.subject.meshLeukocytespt
dc.subject.meshLightpt
dc.subject.meshMalept
dc.subject.meshMicept
dc.subject.meshMice, Inbred NODpt
dc.subject.meshNanoparticlespt
dc.subject.meshPhotosensitizing Agentspt
dc.subject.meshPolyethyleneiminept
dc.subject.meshTretinoinpt
dc.subject.meshU937 Cellspt
dc.subject.meshXenograft Model Antitumor Assayspt
dc.titleProlonged intracellular accumulation of light-inducible nanoparticles in leukemia cells allows their remote activationpt
dc.typearticle-
degois.publication.firstPage15204pt
degois.publication.issue1pt
degois.publication.titleNature Communicationspt
dc.peerreviewedyespt
dc.identifier.doi10.1038/ncomms15204pt
degois.publication.volume8pt
dc.date.embargo2017-05-11*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCMUC - Centre for Mathematics of the University of Coimbra-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-2273-7076-
crisitem.author.orcid0000-0001-8985-9302-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
IIIUC - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais
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