QUINACRINE - SCLEROSING AGENT OF THE UTERO-TUBAL JUNCTION IN WOMEN, WITH ANTICARCINOGENIC ACTIONS IN TRANSPLANTED TUMORS IN MICE

Citation
J. Zipper et al., QUINACRINE - SCLEROSING AGENT OF THE UTERO-TUBAL JUNCTION IN WOMEN, WITH ANTICARCINOGENIC ACTIONS IN TRANSPLANTED TUMORS IN MICE, International journal of gynaecology and obstetrics, 51, 1995, pp. 47-55
Citations number
73
Categorie Soggetti
Obsetric & Gynecology
ISSN journal
00207292
Volume
51
Year of publication
1995
Supplement
1
Pages
47 - 55
Database
ISI
SICI code
0020-7292(1995)51:<47:Q-SAOT>2.0.ZU;2-Q
Abstract
Quinacrine, an acridine derivative that was in widespread use as an an ti-malarial, has been shown to have both sclerosant and anticarcinogen ic actions. The sclerosant action of quinacrine has been used to produ ce occlusion of Fallopian tube in both experimental animals and women, and several clinical studies are reviewed. Both actions of quinacrine are potentiated by steroidal and non-steroidal antiprostaglandins as well as by ionic copper. Combinations of quinacrine with antiprostagla ndin drugs, and also with copper, improved the efficacy of quinacrine when used for female sterilization and reduced side effects. A review of the experimental and epidemiological evidence suggests that quinacr ine has no carcinogenic effects.