Principles in the design of ligand-targeted cancer therapeutics and imaging agents

被引:557
作者
Srinivasarao, Madduri [1 ]
Galliford, Chris V. [1 ]
Low, Philip S. [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
FOLATE RECEPTOR-ALPHA; CIRCULATING TUMOR-CELLS; MEMBRANE ANTIGEN; IN-VIVO; DRUG-DELIVERY; RADIATION-DOSIMETRY; ANTITUMOR-ACTIVITY; PHASE-I; MATRIX METALLOPROTEINASES; LIPOSOMAL DOXORUBICIN;
D O I
10.1038/nrd4519
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Most cancer drugs are designed to interfere with one or more events in cell proliferation or survival. As healthy cells may also need to proliferate and avoid apoptosis, anticancer agents can be toxic to such cells. To minimize these toxicities, strategies have been developed wherein the therapeutic agent is targeted to tumour cells through conjugation to a tumour-cell-specific small-molecule ligand, thereby reducing delivery to normal cells and the associated collateral toxicity. This Review describes the major principles in the design of ligand-targeted drugs and provides an overview of ligand-drug conjugates and ligand-imaging-agent conjugates that are currently in development.
引用
收藏
页码:203 / 219
页数:17
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