Developments with targeted enzymes in cancer therapy

被引:42
作者
Bagshawe, KD
Sharma, SK
Burke, PJ
Melton, RG
Knox, RJ
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Med Oncol, London W6 8RP, England
[2] Def Evaluat & Res Assoc, Enzacta Grp PLC, Salisbury SP4 0JG, Wilts, England
关键词
D O I
10.1016/S0952-7915(99)00004-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cancer therapy based on the delivery of enzymes to tumour sites has advanced in several directions since antibody-directed enzyme/prodrug therapy was first described. It has been shown that methoxypolyethylene glycol (MPEG) can be used to deliver enzyme to a variety of solid tumours. MPEG-enzyme conjugates show reduced immunogenicity and may allow repeated treatment with enzymes of bacterial origin. Enzyme delivery to tumours by polymers can be used to convert a low toxicity prodrug to a potent cytotoxic agent. An example of such a prodrug is CB1954, which can be activated by a human enzyme in the presence of a cosubstrate, Tumour-located enzymes can also be used in conjunction with a combination of antimetabolites and rescue agents. The rescue agent protects normal tissue but is degraded at cancer sites by the enzyme, thus deprotecting the tumour and allowing prolonged antimetabolite action.
引用
收藏
页码:579 / 583
页数:5
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