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Bionano interactions of mcf-7 breast tumor cells with a transferrin receptor targeted nanoparticle.

Abstract
Although transferrin receptor (TfR) is widely accepted as a target for cancer therapy, few studies have elaborated on delivery efficiency of TfR upon interactions with TfR-targeted nanomedicine. Here, a micellar system employing TfR-specific 7peptide (histidine-alanine-isoleucine-tyrosine- proline-arginine-histidine, HAIYPRH, 7pep) as the targeting moiety was constructed; and its endocytosis, intracellular trafficking as well as influence on TfR expression and in vivo tumor targeting were explored in the MCF-7 tumor model. In contrast to unmodified micelles, 7pep modification enhanced the cellular uptake of micelles without altering endocytic pathways, and slowed down the trafficking of micelles to lysosomes without changing the final intracellular colocalization. Interestingly, cellular TfR level was increased by 7pep-modified micelles. Furthermore, receptor saturation and recovery was observed in vivo. In conclusion, this study comprehensively investigated the bionano interaction between TfR positive tumors and 7pep-modified micelles, and provided scientific information for cancer therapy with receptor-mediated nanomedicines.
AuthorsWenwen Du, Yuchen Fan, Bing He, Nan Zheng, Lan Yuan, Wenbing Dai, Hua Zhang, Xueqing Wang, Jiancheng Wang, Xuan Zhang, Qiang Zhang
JournalMolecular pharmaceutics (Mol Pharm) Vol. 12 Issue 5 Pg. 1467-76 (May 04 2015) ISSN: 1543-8392 [Electronic] United States
PMID25811613 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Micelles
  • Peptides
  • Receptors, Transferrin
Topics
  • Cell Membrane (metabolism)
  • Drug Delivery Systems
  • Humans
  • MCF-7 Cells
  • Micelles
  • Nanomedicine (methods)
  • Nanoparticles (chemistry)
  • Peptides (chemistry, metabolism)
  • Receptors, Transferrin (chemistry, metabolism)

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