Abstract |
The anti-oestrogen zindoxifene was originally developed as a drug for the treatment of hormone-dependent mammary carcinomas. Experiments with rats bearing androgen-dependent prostatic tumours revealed anti-neoplastic activity of zindoxifene on these tumours also. Therefore, the inhibitory effect of this drug was studied in various prostatic tumour models in comparison to the anti-oestrogen tamoxifen and to castration. The growth of the hormone-dependent Dunning R3327 H tumour was strongly inhibited by zindoxifene (4 mg/kg), which was more effective than tamoxifen (43% T/C vs 87% T/C, the ratios of tumour weights in control and drug-treated rats). Zindoxifene was able to delay the relapse of these tumours by 7 weeks in comparison to castration. The experiments with Noble Nb-R prostatic tumours showed that administration of zindoxifene (5 mg) is superior to castration (5% T/C vs 52% T/C). The growth of tumours in castrated rats was completely inhibited by administration of zindoxifene. Therefore a peripheral mode of action has to be assumed.
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Authors | M R Schneider, C D Schiller, A Humm, E von Angerer |
Journal | Journal of cancer research and clinical oncology
(J Cancer Res Clin Oncol)
Vol. 117
Issue 1
Pg. 33-6
( 1991)
ISSN: 0171-5216 [Print] Germany |
PMID | 1997466
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Estrogen Antagonists
- Indoles
- Tamoxifen
- zindoxifene
- Diethylstilbestrol
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Topics |
- Adenocarcinoma
(drug therapy)
- Animals
- Antineoplastic Agents
(pharmacology)
- Castration
- Diethylstilbestrol
(pharmacology)
- Estrogen Antagonists
(pharmacology)
- Indoles
(pharmacology)
- Male
- Neoplasm Transplantation
- Neoplasms, Experimental
(drug therapy)
- Neoplasms, Hormone-Dependent
(drug therapy)
- Prostatic Neoplasms
(drug therapy)
- Rats
- Rats, Inbred F344
- Tamoxifen
(pharmacology)
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