NGR-based Strategies for Targeting Delivery of Chemotherapeutics to Tumor Vasculature

ISSN: 1875-5992 (Online)
ISSN: 1871-5206 (Print)


Volume 16, 12 Issues, 2016


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Anti-Cancer Agents in Medicinal Chemistry

Formerly: Current Medicinal Chemistry - Anti-Cancer Agents

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Editor-in-Chief:
Michelle Prudhomme
Universite Blaise Pascal - C.N.R.S
Aubiere Cedex
France


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NGR-based Strategies for Targeting Delivery of Chemotherapeutics to Tumor Vasculature



Anti-Cancer Agents in Medicinal Chemistry, 12(3): 239-246.

Author(s): Mingming Zou, Lei Zhang, Yuanchao Xie and Wenfang Xu.

Affiliation: Department of Medicinal Chemistry, School of Pharmaceutical Sciences, ShanDong University, 44,West Wenhua Road, 250012, Jinan, ShanDong, P.R. China.

Abstract

In the last decades, NGR-containing peptides have been proved useful for ligand-directed targeted delivery of various chemotherapeutic drugs to tumor vasculature. Aminopeptidase N (APN; CD13) has been demonstrated to be a key binding site for NGR peptides on tumor vasculature. For drug targeting, chemical means have been applied to couple NGR-peptides to small molecule drugs, such as cytokines, antiangiogenic compounds, viral particles, contrast agents, DNA complexes and other biologic response modifiers. Some products have shown impressive results in preclinical animal models, such as NGR-TNF which was currently tested in Phase III trials. In this article we will review the process of NGR-to-isoDGR transition and provide suggestions for the design of the diverse NGR peptide-chemotherapeutics conjugates.

Keywords:

NGR-peptides, APN, Angiogenesis, Targeted delivery, Chemotherapeutics, isoDGR, αvβ3-integrin, biodistribution, Asparagine deamidation, Therapeutic Peptides and Proteins.



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Article Details

Volume: 12
Issue Number: 3
First Page: 239
Last Page: 246
Page Count: 8
DOI: 10.2174/187152012800228751
Price: $58
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