Integrin Targeted Delivery of Radiotherapeutics

被引:37
作者
Liu, Zhaofei [2 ,3 ]
Wang, Fan [2 ,3 ]
Chen, Xiaoyuan [1 ]
机构
[1] NIBIB, Lab Mol Imaging & Nanomed, NIH, Bethesda, MD 20892 USA
[2] Peking Univ, Med Isotopes Res Ctr, Beijing 100871, Peoples R China
[3] Peking Univ, Sch Basic Med Sci, Dept Radiat Med, Beijing 100871, Peoples R China
来源
THERANOSTICS | 2011年 / 1卷
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
Cancer; integrin; radionuclide; radioimmunotherapy (RIT); peptide receptor radionuclide therapy (PRRT); HUMANIZED MONOCLONAL-ANTIBODY; IMPROVING TUMOR UPTAKE; ALPHA(V)BETA(3) INTEGRIN; CYSTINE-KNOT; RGD-PEPTIDE; CANCER; THERAPY; EXPRESSION; RECEPTOR; PHARMACOKINETICS;
D O I
10.7150/thno/v01p0201
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Targeted radionuclide therapy, which is based on the selective delivery of a sufficient radiation dose to tumors without significantly affecting normal tissues, is a promising therapeutic approach for the treatment of a wide variety of malignancies. Integrins, a family of cell adhesion molecules, play key roles during tumor angiogenesis and metastasis. Among all the integrins, alpha v beta 3 seems to be the most important in the process of tumor angiogenesis. 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-tumor therapy. In this review, we summarize the current development and applications of antibody-, peptide-, and other ligand-based integrin targeted radiotherapeutics for tumor radiation therapy.
引用
收藏
页码:201 / 210
页数:10
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