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Treatment of experimental DMBA induced mammary carcinoma with Cetrorelix (SB-75): a potent antagonist of luteinizing hormone-releasing hormone.
- Source :
-
Journal of cancer research and clinical oncology [J Cancer Res Clin Oncol] 1992; Vol. 118 (1), pp. 44-9. - Publication Year :
- 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.
- Subjects :
- 9,10-Dimethyl-1,2-benzanthracene
Animals
Antineoplastic Agents administration & dosage
Antineoplastic Agents pharmacology
Antineoplastic Combined Chemotherapy Protocols pharmacology
Cell Survival drug effects
Dose-Response Relationship, Drug
Drug Evaluation, Preclinical
Female
Gonadotropin-Releasing Hormone administration & dosage
Gonadotropin-Releasing Hormone pharmacology
Mammary Neoplasms, Experimental chemically induced
Mammary Neoplasms, Experimental pathology
Rats
Rats, Inbred Strains
Triptorelin Pamoate
Gonadotropin-Releasing Hormone analogs & derivatives
Gonadotropin-Releasing Hormone antagonists & inhibitors
Mammary Neoplasms, Experimental drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 0171-5216
- Volume :
- 118
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of cancer research and clinical oncology
- Publication Type :
- Academic Journal
- Accession number :
- 1530849
- Full Text :
- https://doi.org/10.1007/BF01192310