Cancer siRNA therapy by tumor selective delivery with ligand-targeted sterically stabilized nanoparticle
Parker Hannifin (United States)
Indexed incrossrefdoajpubmed
Abstract
Potent sequence selective gene inhibition by siRNA 'targeted' therapeutics promises the ultimate level of specificity, but siRNA therapeutics is hindered by poor intracellular uptake, limited blood stability and non-specific immune stimulation. To address these problems, ligand-targeted, sterically stabilized nanoparticles have been adapted for siRNA. Self-assembling nanoparticles with siRNA were constructed with polyethyleneimine (PEI) that is PEGylated with an Arg-Gly-Asp (RGD) peptide ligand attached at the distal end of the polyethylene glycol (PEG), as a means to target tumor neovasculature expressing integrins and used to deliver siRNA inhibiting vascular endothelial growth factor receptor-2 (VEGF R2)…
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Authors
1Topics & keywords
Topics
Keywords
- Biology
- Ligand (biochemistry)
- Angiogenesis
- Peptide
- Cancer research
- Small interfering RNA
- Gene delivery
- Oligonucleotide
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