PuSH - Publikationsserver des Helmholtz Zentrums München: RNAi-based glyconanoparticles trigger apoptotic pathways for <em>in vitro</em> and <em>in vivo</em> enhanced cancer-cell killing.

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Conde, J.* ; Tian, F. ; Hernandez, Y.* ; Bao, C.* ; Baptista, P.V.* ; Cui, D.* ; Stöger, T. ; de la Fuente, J.M.*

RNAi-based glyconanoparticles trigger apoptotic pathways for in vitro and in vivo enhanced cancer-cell killing.

Nanoscale 7, 9083-9091 (2015)

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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.

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Gold glyconanoparticles (GlycoNPs) are full of promise in areas like biomedicine, biotechnology and materials science due to their amazing physical, chemical and biological properties. Here, siRNA GlycoNPs (AuNP@PEG@Glucose@siRNA) in comparison with PEGylated GlycoNPs (AuNP@PEG@Glucose) were applied in vitro to a luciferase-CMT/167 adenocarcinoma cancer cell line and in vivo via intratracheal instillation directly into the lungs of B6 albino mice grafted with luciferase-CMT/167 adenocarcinoma cells. siRNA GlycoNPs but not PEGylated GlycoNPs induced the expression of pro-apoptotic proteins such as Fas/CD95 and caspases 3 and 9 in CMT/167 adenocarcinoma cells in a dose dependent manner, independent of the inflammatory response, evaluated by bronchoalveolar lavage cell counting. Moreover, in vivo pulmonary delivered siRNA GlycoNPs were capable of targeting c-Myc gene expression (a crucial regulator of cell proliferation and apoptosis) via in vivo RNAi in tumour tissue, leading to an ∼80% reduction in tumour size without associated inflammation.

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