4.7 Review

The functions and applications of A7R in anti-angiogenic therapy, imaging and drug delivery systems

Journal

ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 14, Issue 6, Pages 595-608

Publisher

SHENYANG PHARMACEUTICAL UNIV
DOI: 10.1016/j.ajps.2019.04.004

Keywords

A7R; Vascular endothelial growth factor receptor 2; Neuropilin-1; Antiangiogenesis; Tumor angiogenesis imaging; Drug delivery

Funding

  1. National Natural Science Foundation of China [81302686]
  2. Primary Research & Developement Plan of Shandong Province [2016GSF201083]

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Vascular endothelial growth factor receptor 2 (VEGFR-2) and neuropilin-1 (NRP-1) are two prominent antiangiogenic targets. They are highly expressed on vascular endothelial cells and some tumor cells. Therefore, targeting VEGFR-2 and NRP-1 may be a potential antiangiogenic and antitumor strategy. A7R, a peptide with sequence of Ala-Thr-Trp-Leu-Pro-Pro-Arg that was found by phage display of peptide libraries, can preferentially target VEGFR-2 and NRP-1 and destroy the binding between vascular endothelial growth factor 165 (VEGF165) and VEGFR-2 or NRP-1. This peptide is a new potent inhibitor of tumor angiogenesis and a targeting ligand for cancer therapy. This review describes the discovery, function and mechanism of the action of A7R, and further introduces the applications of A7R in antitumor angiogenic treatments, tumor angiogenesis imaging and targeted drug delivery systems. In this review, strategies to deliver different drugs by A7R-modified liposomes and nanoparticies are highlighted. A7R, a new dual targeting ligand of VEGFR-2 and NRP-1, is expected to have efficient therapeutic or targeting roles in tumor drug delivery. (C) 2019 Shenyang Pharmaceutical University. Published by Elsevier B.V.

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