Literature DB >> 1530849

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

T Reissmann1, P Hilgard, J H Harleman, J Engel, A M Comaru-Schally, A V Schally.   

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.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1530849     DOI: 10.1007/bf01192310

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  18 in total

1.  New antagonists of LHRH. II. Inhibition and potentiation of LHRH by closely related analogues.

Authors:  S Bajusz; V J Csernus; T Janaky; L Bokser; M Fekete; A V Schally
Journal:  Int J Pept Protein Res       Date:  1988-12

Review 2.  Biological and molecular bases of mammary carcinogenesis.

Authors:  J Russo; I H Russo
Journal:  Lab Invest       Date:  1987-08       Impact factor: 5.662

3.  Treatment of endometriosis with a delayed release preparation of the agonist D-Trp6-luteinizing hormone-releasing hormone: long-term follow-up in a series of 50 patients.

Authors:  J R Zorn; J Mathieson; F Risquez; A M Comaru-Schally; A V Schally
Journal:  Fertil Steril       Date:  1990-03       Impact factor: 7.329

4.  Reproductive/endocrine and anaphylactoid properties of an LHRH-antagonist, ORF 18260 [Ac-DNAL1(2), 4FDPhe2,D-Trp3,D-Arg6]-GnRH.

Authors:  D W Hahn; J L McGuire; W W Vale; J Rivier
Journal:  Life Sci       Date:  1985-08-12       Impact factor: 5.037

5.  Reversible hypogonadism induced by a luteinizing hormone-releasing hormone (LH-RH) agonist (Buserelin) as a new therapeutic approach for endometriosis.

Authors:  A Lemay; R Maheux; N Faure; C Jean; A T Fazekas
Journal:  Fertil Steril       Date:  1984-06       Impact factor: 7.329

6.  [Ac-D-NAL(2)1,4FD-Phe2,D-Trp3,D-Arg6]-LHRH, a potent antagonist of LHRH, produces transient edema and behavioral changes in rats.

Authors:  F Schmidt; K Sundaram; R B Thau; C W Bardin
Journal:  Contraception       Date:  1984-03       Impact factor: 3.375

7.  Regression of rat mammary tumors effected by a gonadoliberin analog.

Authors:  E R DeSombre; E S Johnson; W F White
Journal:  Cancer Res       Date:  1976-10       Impact factor: 12.701

8.  Highly potent antagonists of luteinizing hormone-releasing hormone free of edematogenic effects.

Authors:  S Bajusz; M Kovacs; M Gazdag; L Bokser; T Karashima; V J Csernus; T Janaky; J Guoth; A V Schally
Journal:  Proc Natl Acad Sci U S A       Date:  1988-03       Impact factor: 11.205

9.  Inhibition of growth of human mammary tumor cells by potent antagonists of luteinizing hormone-releasing hormone.

Authors:  Y Sharoni; E Bosin; A Miinster; J Levy; A V Schally
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

10.  THE RESPONSE OF EXPERIMENTALLY INDUCED MAMMARY TUMOURS IN RATS TO HYPOPHYSECTOMY AND TO PITUITARY STALK SECTION.

Authors:  P M DANIEL; M M PRICHARD
Journal:  Br J Cancer       Date:  1963-09       Impact factor: 7.640

View more
  3 in total

1.  Evaluation of Orntide microspheres in a rat animal model and correlation to in vitro release profiles.

Authors:  J W Kostanski; B A Dani; G A Reynolds; C Y Bowers; P P DeLuca
Journal:  AAPS PharmSciTech       Date:  2000-10-01       Impact factor: 3.246

2.  Evaluating the response to antioestrogen toremifene treatment in DMBA induced rat mammary carcinoma.

Authors:  R Huovinen; P L Kellokumpu-Lehtinen; Y Collan
Journal:  Int J Exp Pathol       Date:  1994-08       Impact factor: 1.925

Review 3.  Treatment of Breast Cancer With Gonadotropin-Releasing Hormone Analogs.

Authors:  Maira Huerta-Reyes; Guadalupe Maya-Núñez; Marco Allán Pérez-Solis; Eunice López-Muñoz; Nancy Guillén; Jean-Christophe Olivo-Marin; Arturo Aguilar-Rojas
Journal:  Front Oncol       Date:  2019-10-01       Impact factor: 6.244

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.