Literature DB >> 7868662

The effects of ICI 182,780, a pure anti-oestrogen, on the hypothalamic-pituitary-gonadal axis and on endometrial proliferation in pre-menopausal women.

E J Thomas1, P L Walton, N M Thomas, M Dowsett.   

Abstract

ICI 182,780 has shown pure oestrogen antagonism in vitro and in vivo in animals. A total of 17 women with normal menstrual cycles were administered ICI 182,780, 12 mg daily for 7 days in the follicular phase prior to hysterectomy; 11 normal women were used as controls. Of the 17 patients, three (18%) experienced a luteinizing hormone (LH) surge in the treatment group compared with five (45%) in the controls (P = 0.24), and these patients were only included up to the surge. There were no differences in the daily mean plasma LH and follicle stimulating hormone concentrations between the treatment (n = 17) and control (n = 10) groups. The mean plasma oestradiol was higher in the treatment group than controls (P < 0.05) on days 5, 6 and 7. However, there was no increase in endometrial thickness in the treatment group throughout the study. In the control group, endometrial thickness increased during the study and was significantly higher (P < 0.05) on day 7. There was no ultrasonic evidence of ovarian hyperstimulation and no serious adverse events reported. This study shows that treatment for 7 days with ICI 182,780 does not cause ovarian hyperstimulation and has a potent anti-oestrogenic action on the endometrium. We conclude that ICI 182,780 may be a useful compound in the treatment of oestrogen-dependent gynaecological disease.

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Year:  1994        PMID: 7868662     DOI: 10.1093/oxfordjournals.humrep.a138380

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  6 in total

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Authors:  D de Valeriola; A Awada; J A Roy; A Di Leo; L Biganzoli; M Piccart
Journal:  Drugs       Date:  1997-09       Impact factor: 9.546

Review 2.  Fulvestrant.

Authors:  M Curran; L Wiseman
Journal:  Drugs       Date:  2001       Impact factor: 9.546

3.  Estrogen-like potentiation of ghrelin-stimulated GH secretion by fulvestrant, a putatively selective ER antagonist, in postmenopausal women.

Authors:  Johannes D Veldhuis; Rebecca J Yang; Jean R Wigham; Dana Erickson; John C Miles; Cyril Y Bowers
Journal:  J Clin Endocrinol Metab       Date:  2014-12       Impact factor: 5.958

Review 4.  Fulvestrant: a review of its use in hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following antiestrogen therapy.

Authors:  Kate McKeage; Monique P Curran; Greg L Plosker
Journal:  Drugs       Date:  2004       Impact factor: 9.546

5.  Differential hormonal regulation of estrogen receptors ERalpha and ERbeta and androgen receptor expression in rat efferent ductules.

Authors:  Cleida A Oliveira; Germán A B Mahecha; Kay Carnes; Gail S Prins; Philippa T K Saunders; Luiz R França; Rex A Hess
Journal:  Reproduction       Date:  2004-07       Impact factor: 3.906

6.  Estrogen stimulates adenosine receptor expression subtypes in human breast cancer MCF-7 cell line.

Authors:  Azam Mohamadi; Mahmoud Aghaei; Mojtaba Panjehpour
Journal:  Res Pharm Sci       Date:  2018-02
  6 in total

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