酶介导的肿瘤选择性治疗前药的开发。

K Jin Yoon, Philip M Potter, Mary K Danks
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引用次数: 9

摘要

抗癌酶/前药治疗方法旨在特异性激活肿瘤位点的前药,以最小的毒性实现抗肿瘤反应。迄今为止,这些方法取得的不确定的成功促使人们寻找更有效的组合。这篇迷你综述评价和比较了七种选定的酶/前药组合的特性,并讨论了未来开发有效组合的目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of prodrugs for enzyme-mediated, tumor-selective therapy.

Anticancer enzyme/prodrug approaches to therapy are designed to activate prodrugs specifically at tumor loci, to achieve antitumor responses with minimal toxicity. The equivocal success of these approaches thus far has led to searches for more efficient combinations. This mini-review evaluates and compares characteristics of seven selected enzyme/prodrug combinations, and discusses goals for future development of effective combinations.

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