Abstract |
An inhibitory effect of TZP-4238, a newly synthesized antiandrogen, on the growth of Dunning R3327 rat prostatic tumor was studied and compared with that of chlormadinone acetate (CMA). TZP-4238 markedly suppressed the growth of R3327 tumor. The inhibitory effect of TZP-4238 on the tumor was more potent than that on the prostate. While the inhibitory effect of TZP-4238 on the weight of the ventral prostate was about 6 times as great as that of CMA, the suppressive effect of TZP-4238 on tumor weight was about 40 times as great as that of CMA. Serum levels of testosterone and dihydrotestosterone showed no obvious changes after the administration of either TZP-4238 or CMA. The inhibitory effect of TZP-4238 on the growth of R3327 tumor indicated the application of the compound to human prostatic cancer.
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Authors | T Ichikawa, S Akimoto, J Shimazaki |
Journal | Endocrine journal
(Endocr J)
Vol. 40
Issue 4
Pg. 425-30
(Aug 1993)
ISSN: 0918-8959 [Print] Japan |
PMID | 7522799
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Androgen Antagonists
- Androgens
- Dihydrotestosterone
- Chlormadinone Acetate
- Testosterone
- osaterone acetate
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Topics |
- Administration, Oral
- Androgen Antagonists
(administration & dosage, therapeutic use)
- Androgens
(metabolism)
- Animals
- Chlormadinone Acetate
(administration & dosage, analogs & derivatives, therapeutic use)
- Dihydrotestosterone
(blood)
- Male
- Neoplasms, Hormone-Dependent
(drug therapy, metabolism, pathology)
- Orchiectomy
- Organ Size
(drug effects)
- Prostate
(drug effects, pathology)
- Prostatic Neoplasms
(drug therapy, metabolism, pathology)
- Rats
- Testis
(drug effects, pathology)
- Testosterone
(blood)
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