Receptor-mediated and enzyme-dependent targeting of cytotoxic anticancer drugs

被引:233
作者
Dubowchik, GM [1 ]
Walker, MA [1 ]
机构
[1] Bristol Myers Squibb Co, Pharmaceut Res Inst, Wallingford, CT 06492 USA
关键词
antitumor; antibody; prodrug; drug delivery; immunoconjugate; drug release;
D O I
10.1016/S0163-7258(99)00018-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review is a survey of various approaches to targeting cytotoxic anticancer drugs to tumors primarily through biomolecules expressed by cancer cells or associated vasculature and stroma. These include monoclonal antibody immunoconjugates; enzyme prodrug therapies, such as antibody-directed enzyme prodrug therapy, gene-directed enzyme prodrug therapy, and bacterial-directed enzyme prodrug therapy; and metabolism-based therapies that seek to exploit increased tumor expression of, e.g., proteases, low-density lipoprotein receptors, hormones, and adhesion molecules. Following a discussion of factors that positively and negatively affect drug delivery to solid tumors, we concentrate on a mechanistic understanding of selective drug release or generation at the tumor site. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:67 / 123
页数:57
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