Title of article
Developments with targeted enzymes in cancer therapy
Author/Authors
Kenneth D Bagshawe، نويسنده , , Surinder M. Sharma، نويسنده , , Philip J Burke، نويسنده , , Roger G Melton، نويسنده , , Richard J Knox، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1999
Pages
5
From page
579
To page
583
Abstract
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.
Journal title
Current Opinion in Immunology
Serial Year
1999
Journal title
Current Opinion in Immunology
Record number
511887
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