Effects of an androgenic derivative on pre-established mammary tumours chemically induced in the rat

In: Journal of Cancer Research and Clinical Oncology · 1991 · vol. 117(6) , pp. 575–582 · doi:10.1007/bf01613291 · PMID:1744164 · W2007827161
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Danazol treatment reduced the incidence, number, and volume of chemically induced malignant mammary tumors in rats, without affecting benign tumors or ovarian function.

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The study examined how danazol, an androgenic derivative, affects pre-established dimethylbenz[a]anthracene-induced mammary tumours in rats by administering 10–12 mg kg−1 day−1 for 97 days and assessing ovarian function and tumour outcomes. Danazol did not influence ovarian function by the end of the assay, but it reduced the incidence of malignant mammary tumours (P<0.05), the number of tumours (P<0.05), and malignant tumour volume, while benign and “doubtful expression” tumour parameters were similar between groups. The authors attribute this differential effect to differences in incidence and/or receptor content between tumour types, framing a mechanistic hypothesis based on danazol’s behaviour at multiple receptor levels. This paper is centrally about endometriosis and/or adenomyosis— it does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Summary The effects were studied of an androgenic derivative — danazol — administered at doses of 10–12 mg kg−1 day−1 during 97 days to rats with dimethylbenz[a] anthracene-induced mammary tumours. Our main observations were as follows. (a) Danazol did not influence ovarian function at the end of the assay. (b) The treatment with danazol reduced the incidence (P<0.05), number of tumours (P<0.05) and volume of malignant mammary tumours; on the other hand, the values of these parameters for benign tumours and those of doubtful expression were similar in both experimental groups. (c) Such differential action of Danazol seems to be due to the different incidence and/or content of receptors of both types of tumours. (d) The latter results lead to a hypothesis for the mechanism of action of danazol based on its behaviour at different levels. 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Br J Cancer 53:629–636 Wood GP, Wu ChH, Flickinger GL, Mikhail G (1975) Hormonal changes associated with danazol therapy: Obstet Gynecol 45:302–304 Yen SSC (1983) Clinical applications of gonadotropine-releasing hormone and gonadotropin-releasing hormone analogs. Fertil Steril 39:257–266 Author information Authors and Affiliations Rights and permissions About this article Cite this article Escrich, E., Ribalta, T., Muntané, J. et al. Effects of an androgenic derivative on pre-established mammary tumours chemically induced in the rat. J Cancer Res Clin Oncol 117, 575–582 (1991). https://doi.org/10.1007/BF01613291 Received: Accepted: Issue date: DOI: https://doi.org/10.1007/BF01613291

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