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Cited by 323

The DOI matches its Crossref record; 78 of the 78 references it cites were found in a registry or an index.

Integrin αvβ3‐targeted cancer therapy

Open access
Liu, Zhaofei, Wang, Fan, Chen, Xiaoyuan·2008·Drug Development Research

Abstract

Anti‐angiogenesis is a promising strategy for the treatment of cancer. Integrins, consisting of two noncovalently bound transmembrane α and β subunits, are an important molecular family involved in tumor angiogenesis. The blockade of integrin signaling has been demonstrated to be efficient to inhibit tumor growth, angiogenesis, and metastasis. Among all the integrins, α v β 3 seems to be the most important one during tumor angiogenesis. The inhibition of integrin α v β 3 signaling with antibodies, peptides, peptidomimetics, and other antagonists has great potential in the treatment of cancer. In addition, integrin α v β 3 is highly expressed on activated endothelial cells, new‐born vessels as well as some tumor cells, but is not present in resting endothelial cells and most normal organ systems, making it a suitable target for anti‐angiogenic therapy. In this article we will review the role of integrin α v β 3 in angiogenesis, present recent progress in the use of integrin α v β 3 antagonists and integrin‐targeted delivery systems as potential cancer therapeutics, and discuss future perspectives. Drug Dev Res 69:329–339, 2008. © 2008 Wiley‐Liss, Inc.

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Metadata

Authors
Liu, Z., Wang, F., & Chen, X.
Venue
Drug Development Research
Publisher
Wiley
Published
2008-09
Volume
69
Issue
6
Pages
329-339
ISSN
  • 0272-4391 (ISSN-L)
  • 1098-2299
OpenAlex
W2140859605
Cited by
323
References
78
FWCI
1.84
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Integrin αvβ3‐targeted cancer therapy. https://app.cochat.ai/papers/10.1002/ddr.20265
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Liu, Z., Wang, F., & Chen, X. (2008). Integrin αvβ3‐targeted cancer therapy. Drug Development Research. https://doi.org/10.1002/ddr.20265

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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