Gene therapy of cancer:: Activation of nucleoside prodrugs with E-coli purine nucleoside phosphorylase

被引:31
|
作者
Secrist, JA [1 ]
Parker, WB
Allan, PW
Bennett, LL
Waud, WR
Truss, JW
Fowler, AT
Montgomery, JA
Ealick, SE
Wells, AH
Gillespie, GY
Gadi, VK
Sorscher, EJ
机构
[1] So Res Inst, Birmingham, AL 35255 USA
[2] Cornell Univ, Ithaca, NY USA
[3] Univ Alabama, Birmingham, AL USA
来源
NUCLEOSIDES & NUCLEOTIDES | 1999年 / 18卷 / 4-5期
关键词
D O I
10.1080/15257779908041562
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During the last few years, many gene therapy strategies have been developed for various disease targets. The development of anticancer gene therapy strategies to selectively generate cytotoxic nucleoside or nucleotide analogs is an attractive goal. One such approach involves the delivery of herpes simplex virus thymidine kinase followed by the acyclic nucleoside analog ganciclovir. We have developed another gene therapy methodology for the treatment of cancer that has several significant attributes. Specifically, our approach involves the delivery off. coli purine nucleoside phosphorylase, followed by treatment with a relatively non-toxic nucleoside prodrug that is cleaved by the enzyme to a toxic compound. This presentation describes the concept, details our search for suitable prodrugs, and summarizes the current biological data.
引用
收藏
页码:745 / 757
页数:13
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