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Viral nanoparticles decorated with novel EGFL7 ligands enable intravital imaging of tumor neovasculature.


ABSTRACT: Angiogenesis is a dynamic process fundamental to the development of solid tumors. Epidermal growth factor-like domain 7 (EGFL7) is a protein whose expression is restricted to endothelial cells undergoing active remodeling that has emerged as a key mediator of this process. EGFL7 expression is associated with poor outcome in several cancers, making it a promising target for imaging or therapeutic strategies. Here, EGFL7 is explored as a molecular target for active neovascularization. Using a combinatorial peptide screening approach, we describe the discovery and characterization of a novel high affinity EGFL7-binding peptide, E7p72, that specifically targets human endothelial cells. Viral nanoparticles decorated with E7p72 peptides specifically target tumor-associated neovasculature with high specificity as assessed by intravital imaging. This work highlights the value of EGFL7 as a target for angiogenic vessels and opens the door for novel targeted therapeutic approaches.

SUBMITTER: Cho CF 

PROVIDER: S-EPMC5770569 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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Viral nanoparticles decorated with novel EGFL7 ligands enable intravital imaging of tumor neovasculature.

Cho Choi-Fong CF   Yu Lihai L   Nsiama Tienabe K TK   Kadam Alisha N AN   Raturi Arun A   Shukla Sourabh S   Amadei Giulio A GA   Steinmetz Nicole F NF   Luyt Leonard G LG   Lewis John D JD  

Nanoscale 20170801 33


Angiogenesis is a dynamic process fundamental to the development of solid tumors. Epidermal growth factor-like domain 7 (EGFL7) is a protein whose expression is restricted to endothelial cells undergoing active remodeling that has emerged as a key mediator of this process. EGFL7 expression is associated with poor outcome in several cancers, making it a promising target for imaging or therapeutic strategies. Here, EGFL7 is explored as a molecular target for active neovascularization. Using a comb  ...[more]

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