Bioresponsive cancer-targeted polysaccharide nanosystem to inhibit angiogenesis
Fang Yang, Xueyang Fang, Wenting Jiang, Tianfeng Chen Department of Chemistry, Jinan University, Guangzhou, China Abstract: With many desirable features, such as being more effective and having multiple effects, antiangiogenesis has become one of the promising cancer treatments. The aim of this st...
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| Auteurs principaux: | , , , |
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| Format: | article |
| Langue: | EN |
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Dove Medical Press
2017
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| Accès en ligne: | https://doaj.org/article/3222de9c550845e589b30c0cd48c76b8 |
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| Résumé: | Fang Yang, Xueyang Fang, Wenting Jiang, Tianfeng Chen Department of Chemistry, Jinan University, Guangzhou, China Abstract: With many desirable features, such as being more effective and having multiple effects, antiangiogenesis has become one of the promising cancer treatments. The aim of this study was to design and synthesize a new targeted bioresponsive nanosystem with antiangiogenesis properties. The mUPR@Ru(POP) nanosystem was constructed by the polymerization of Ulva lactuca polysaccharide and N-isopropyl acrylamide, decorated with methoxy polyethylene glycol and Arg–Gly–Asp peptide, and encapsulated with anticancer complex [Ru(phen)2p-MOPIP](PF6)2·2H2O. The nanosystem was both pH responsive and targeted. Therefore, the cellular uptake of the drug was greatly improved. Moreover, the mUPR@Ru(POP) had strong suppressive effects against vascular endothelial growth factor (VEGF)-induced angiogenesis through apoptosis. The mUPR@Ru(POP) significantly inhibited VEGF-induced human umbilical vein endothelial cell migration, invasion, and tube formation. These findings have presented new insights into the development of antiangiogenesis drugs. Keywords: polysaccharide nanosystem, antiangiogenesis, cancer-targeted, bioresponsive |
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