Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1992;118(1):44-9.
doi: 10.1007/BF01192310.

Treatment of experimental DMBA induced mammary carcinoma with Cetrorelix (SB-75): a potent antagonist of luteinizing hormone-releasing hormone

Affiliations

Treatment of experimental DMBA induced mammary carcinoma with Cetrorelix (SB-75): a potent antagonist of luteinizing hormone-releasing hormone

T Reissmann et al. J Cancer Res Clin Oncol. 1992.

Abstract

Cetrorelix, (Ac-D-Nal(2)1, D-Phe(4Cl)2, D-Pal(3)3, D-Cit6, D-Ala10)-LHRH (SB-75) is a new highly potent antagonist of LH-RH. In the model of DMBA-induced mammary carcinoma, this antagonist was very effective in reducing tumor mass. A rapid decrease in tumor weights to levels below 0.1 g total tumor mass was achieved with 300 micrograms/kg given sc. daily for 14 days. The weights of uteri and ovaries were reduced to about 40-50% of control values. In all treated rats the estrus cycle was interrupted and the animals remained in a state of anestrus. Microscopically, the effects of Cetrorelix on the tumors were characterized by a loss of mitotic activity, marked regression with apoptosis, an increase of stroma and differentiation towards a normal mammary architecture. On the basis of a dose-response curve, a dose of 100 micrograms/kg/d of Cetrorelix was determined as sufficient for a full antitumor response. Large DMBA-tumors with total tumor mass of about 6 g could also be treated very effectively with a dose of 100 micrograms/kg/d. To achieve a complete tumor regression, the treatment had to last 34 days. After the cessation of treatment with 100 micrograms/kg/d and regrowth of the tumors the animals were treated with the agonist Decapeptyl (Trp6-LHRH) using a dose of 50 micrograms/rat/d for 14 days. Again, the tumors responded well and regressed within 10 days. The treatment with an overlapping dose schedule of Cetrorelix and Decapeptyl showed a continuous antitumor response. A transient stimulation of tumor growth by the LH-RH agonist was not observed under these experimental conditions. In ovariectomized rats bearing DMBA-tumors, treatment with Cetrorelix and estradiol, produced no tumor growth inhibition as compared to estradiol control group, indicating that there is no estrogen nullifying effect of this antagonist on tumor cells in this model. On the basis of these results, Cetrorelix is a highly effective antitumor agent in this breast cancer model, which might also be useful under clinical conditions.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Bajusz S, Csernus VJ, Janaky T, Bokser L, Fekete M, Schally AV (1988a) New antagonists of LHRH. Int J Peptide Res 32:425–435 - PubMed
    1. Bajusz S, Kovacs M, Gazdag M, Bokser L, Karashima T, Csernus VJ, Janaky T, Guoth J, Schally AV (1988b) Highly potent antagonists of luteinizing hormone-releasing hormone free of edematogenic effects. Proc Natl Acad Sci 85:1637–1641 - PMC - PubMed
    1. Daniel PM, Prichard MLM (1963) The response of experimentally induced mammary tumors in rats to hypophysectomy and to pituitary stalk section. Br J Cancer 17:446–453 - PMC - PubMed
    1. Debruyne FMJ, Weil EHJ, Del Moral F (1987) Clinical res8lts with the depot preparation of Zoladex in prostate cancer. In: Klijn JGM et al. (ed) Hormonal manipulation of cancer: peptides, growth factors, and new (anti) steroidal agents. Raven Press, New York, p 255
    1. DeSombre ER, Johnson ES, White WF (1976) Regression of rat mammary tumors effected by a gonadoliberin analog. Cancer Res 36:3830–3833 - PubMed

MeSH terms

LinkOut - more resources