Multifunctional albumin-stabilized gold nanoclusters for the reduction of cancer stem cells
Entity
UAM. Departamento de BiologíaPublisher
MDPI AGDate
2019-07-10Citation
10.3390/cancers11070969
Cancers 11.7 (2019): 969
ISSN
2072-6694DOI
10.3390/cancers11070969Funded by
This research was funded by the Spanish Ministry of Economy and Competitiveness (CTQ2016-78454-C2-2-R, SAF2014-56763-R, and SAF2017-87305-R), Comunidad de Madrid (S2013/MIT-2850), Asociación Española Contra el Cáncer, and IMDEA Nanociencia IMDEA Nanociencia acknowledges support from the ‘Severo Ochoa’ Programme for Centres of Excellence in R&D (MINECO, Grant SEV-2016-0686)Project
Gobierno de España. CTQ2016-78454-C2-2-R; Gobierno de España. SAF2014-56763-R; Gobierno de España. SAF2017-87305-R; Comunidad de Madrid. S2013/MIT-2850/NANOFRONTMAG-CM; Gobierno de España. SEV-2016-0686Editor's Version
https://doi.org/10.3390/cancers11070969Subjects
CSCs; DOX; Drug delivery; Nanomedicine; SN38; Stimuli-responsive; Biología y Biomedicina / BiologíaRights
© 2019 by the authors. Licensee MDPI, Basel, Switzerland.Abstract
Controlled delivery of multiple chemotherapeutics can improve the effectiveness of treatments and reduce side effects and relapses. Here in, we used albumin-stabilized gold nanoclusters modified with doxorubicin and SN38 (AuNCs-DS) as combined therapy for cancer. The chemotherapeutics are conjugated to the nanostructures using linkers that release them when exposed to different internal stimuli (Glutathione and pH). This system has shown potent antitumor activity against breast and pancreatic cancer cells. Our studies indicate that the antineoplastic activity observed may be related to the reinforced DNA damage generated by the combination of the drugs. Moreover, this system presented antineoplastic activity against mammospheres, a culturing model for cancer stem cells, leading to an efficient reduction of the number of oncospheres and their size. In summary, the nanostructures reported here are promising carriers for combination therapy against cancer and particularly to cancer stem cells.
Files in this item
Google Scholar:Latorre, Ana
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Latorre, Alfonso
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Castellanos, Milagros
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Diaz, Ciro Rodriguez
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Lazaro-Carrillo, Ana
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Aguado, Tania
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Lecea, Mercedes
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Romero-Pérez, Sonia
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Calero, Macarena
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Sanchez-Puelles, José María
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Villanueva Oroquieta, Ángeles
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Somoza, Álvaro
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