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Three-Dimensional (3D) Tumor Spheroid Invasion Assay
Published on: May 1, 2015
Integrin alpha(v)beta(3)-Targeted Cancer Therapy
Zhaofei Liu1, Fan Wang, Xiaoyuan Chen
1Department of Radiology, Molecular Imaging Program at Stanford (MIPS), Biophysics, and Bio-X Program, Stanford University School of Medicine, Stanford, CA 94305.
Abstract:
Anti-angiogenesis is a promising strategy for the treatment of cancer. Integrins, consisting of two noncovalently bound transmembrane alpha and beta 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, alpha(v)beta(3) seems to be the most important one during tumor angiogenesis. The inhibition of integrin alpha(v)beta(3) signaling with antibodies, peptides, peptidomimetics, and other antagonists has great potential in the treatment of cancer. In addition, integrin alpha(v)beta(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 alpha(v)beta(3) in angiogenesis, present recent progress in the use of integrin alpha(v)beta(3) antagonists and integrin-targeted delivery systems as potential cancer therapeutics, and discuss future perspectives.
Insights
Targeting integrin alpha(v)beta(3) offers a promising anti-angiogenesis strategy for cancer treatment. Blocking this integrin shows potential in inhibiting tumor growth, angiogenesis, and metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Integrins are crucial molecular players in tumor angiogenesis.
- Integrin alpha(v)beta(3) is particularly significant in this process.
- Blocking integrin signaling can inhibit tumor growth, angiogenesis, and metastasis.
Purpose of the Study:
- To review the role of integrin alpha(v)beta(3) in angiogenesis.
- To present recent advancements in using integrin alpha(v)beta(3) antagonists for cancer therapy.
- To discuss integrin-targeted delivery systems and future perspectives in cancer therapeutics.
Main Methods:
- Review of scientific literature on integrin alpha(v)beta(3) and angiogenesis.
- Analysis of studies involving integrin alpha(v)beta(3) antagonists (antibodies, peptides, peptidomimetics).
- Examination of integrin-targeted delivery systems for cancer therapeutics.
Main Results:
- Integrin alpha(v)beta(3) is highly expressed on activated endothelial cells and tumor neovasculature.
- Inhibition of integrin alpha(v)beta(3) signaling demonstrates efficacy in preclinical models.
- Integrin alpha(v)beta(3) antagonists show potential as targeted anti-cancer agents.
Conclusions:
- Integrin alpha(v)beta(3) is a validated target for anti-angiogenic cancer therapy.
- Various antagonists and targeted delivery systems are being developed for clinical application.
- Further research into integrin alpha(v)beta(3) blockade holds promise for improved cancer treatment outcomes.
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