Tumor-targeting peptides from combinatorial libraries

被引:131
|
作者
Liu, Ruiwu [1 ,2 ]
Li, Xiaocen [1 ,2 ]
Xiao, Wenwu [1 ,2 ]
Lam, Kit S. [1 ,2 ,3 ]
机构
[1] Univ Calif Davis, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Ctr Comprehens Canc, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Dept Internal Med, Div Hematol & Oncol, Sacramento, CA 95817 USA
关键词
Tumor-targeting peptide; Biological library; Phage-display peptide library; One-bead one-compound peptide library; High throughput screening; Cell surface receptor; GROWTH-FACTOR RECEPTOR; CYSTINE-KNOT PEPTIDES; CHRONIC LYMPHOCYTIC-LEUKEMIA; PHAGE DISPLAY LIBRARY; ONE-COMPOUND LIBRARY; BREAST-CANCER CELLS; IN-VITRO SELECTION; HIGH-AFFINITY; BINDING PEPTIDE; HOMING PEPTIDE;
D O I
10.1016/j.addr.2016.05.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer is one of the major and leading causes of death worldwide. Two of the greatest challenges in fighting cancer are early detection and effective treatments with no or minimum side effects. Widespread use of targeted therapies and molecular imaging in clinics requires high affinity, tumor-specific agents as effective targeting vehicles to deliver therapeutics and imaging probes to the primary ormetastatic tumor sites. Combinatorial libraries such as phage-display and one-bead one-compound (OBOC) peptide libraries are powerful approaches in discovering tumor-targeting peptides. This review gives an overview of different combinatorial library technologies that have been used for the discovery of tumor-targeting peptides. Examples of tumor-targeting peptides identified from each combinatorial library method will be discussed. Published tumor-targeting peptide ligands and their applications will also be summarized by the combinatorial library methods and their corresponding binding receptors. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:13 / 37
页数:25
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