PRECLINICAL AND CLINICAL PERSPECTIVES ON THE USE OF ESTRAMUSTINE AS AN ANTIMITOTIC DRUG

被引:30
作者
TEW, KD
GLUSKER, JP
HARTLEYASP, B
HUDES, G
SPEICHER, LA
机构
[1] FOX CHASE CANC CTR, DEPT MOLEC STRUCT, PHILADELPHIA, PA 19111 USA
[2] FOX CHASE CANC CTR, DEPT MED ONCOL, PHILADELPHIA, PA 19111 USA
[3] KABI PHARM THERAPEUT AB, S-22363 LUND, SWEDEN
关键词
D O I
10.1016/0163-7258(92)90023-S
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A variety of cell biological, pharmacological, crystallographic and clinical approaches have indicated that the antimitotic drug estramustine has interesting and unusual properties. Although designed as an alkylating agent, the marked stability of the carbamate linkage to the steroid carrier molecule prevents the formation of alkylating intermediates. The affinity of the parent molecule for microtubule associated proteins and the concomitant antimicrotubule activity have cytotoxic consequences in tumor cells. Both preclinical and clinical studies of estramustine in combination with other antimicrotubule agents have shown that this approach has great potential to achieve therapeutic advantage, especially in disease states such as hormone refractory prostate cancer.
引用
收藏
页码:323 / 339
页数:17
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