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dc.contributor.authorGarcía Hevia, Lorena es_ES
dc.contributor.authorVillegas Sordo, Juan Carlos es_ES
dc.contributor.authorFernández Fernández, Fidel Ángel es_ES
dc.contributor.authorCasafont Parra, Íñigo es_ES
dc.contributor.authorGonzález Gómez, Jesús Antonio es_ES
dc.contributor.authorValiente Barroso, Rafael es_ES
dc.contributor.authorLópez Fanarraga, Mónica es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-04-05T17:47:41Z
dc.date.available2023-04-05T17:47:41Z
dc.date.issued2016-02-11es_ES
dc.identifier.issn2192-2640es_ES
dc.identifier.issn2192-2659es_ES
dc.identifier.otherMAT2012-38664-C02-01es_ES
dc.identifier.urihttps://hdl.handle.net/10902/28478
dc.description.abstractUnderstanding the molecular mechanisms underlying the biosynthetic interactions between particular nanomaterials with specific cells or proteins opens new alternatives in nanomedicine and nanotoxicology. Multiwalled carbon nanotubes (MWCNTs) have long been explored as drug delivery systems and nanomedicines against cancer. There are high expectations for their use in therapy and diagnosis. These filaments can translocate inside cultured cells and intermingle with the protein nanofilaments of the cytoskeleton, interfering with the biomechanics of cell division mimicking the effect of traditional microtubule-binding anti-cancer drugs such as paclitaxel. Here, it is shown how MWCNTs can trigger significant anti-tumoral effects in vivo, in solid malignant melanomas produced by allograft transplantation. Interestingly, the MWCNT anti-tumoral effects are maintained even in solid melanomas generated from paclitaxel-resistant cells. These findings provide great expectation in the development of groundbreaking adjuvant synthetic microtubule-stabilizing chemotherapies to overcome drug resistance in cancer.es_ES
dc.description.sponsorshipAcknowledgements: We thank Dr. E. Flahaut for providing the MWCNTs. We are grateful to the Nikon A1R Laser Microscopy Unit of the IDIVAL Institute for the electron microscopy and confocal/time-lapse microscopy, and to M. Aramburu and J. Díaz-Gómez for their help. This work has been supported by the Spanish MINECO and European Union FEDER under Projects ref. PI13/01074 (AES 2013) and MAT2012-38664-C02-01. We especially thank the Fundación Eugenio Rodríguez Pascual (ref “Ayudas de investigación” 2014).es_ES
dc.format.extent21 p.es_ES
dc.language.isoenges_ES
dc.publisherWiley-VCH Verlages_ES
dc.rights© Wiley-VCH Verlages_ES
dc.sourceAdvanced Healthcare Materials 2016, 5, 1080-1087es_ES
dc.subject.otherCanceres_ES
dc.subject.otherAntineoplastic agentes_ES
dc.subject.otherTubulines_ES
dc.subject.otherAnti-proliferativees_ES
dc.subject.otherBiomimetices_ES
dc.titleMultiwalled Carbon Nanotubes inhibit tumor progression in a mouse modeles_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1002/adhm.201500753es_ES
dc.type.versionacceptedVersiones_ES


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