Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist.

Experiments were undertaken with DMBA-induced mammary tumours of the rat to determine the anti-tumour properties of a new and potent luteinizing hormone releasing hormone (LH-RH) agonist, [D-Ser(But) 6Azgly10]-LH-RH (ICI 118630). Tumours were classified according to their oestrogen-receptor (ER) con...

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Main Authors: Nicholson, R. I., Maynard, P. V.
Format: Online
Language:English
Published: 1979
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009890/
id pubmed-2009890
recordtype oai_dc
spelling pubmed-20098902009-09-10 Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist. Nicholson, R. I. Maynard, P. V. Research Article Experiments were undertaken with DMBA-induced mammary tumours of the rat to determine the anti-tumour properties of a new and potent luteinizing hormone releasing hormone (LH-RH) agonist, [D-Ser(But) 6Azgly10]-LH-RH (ICI 118630). Tumours were classified according to their oestrogen-receptor (ER) content. Twice daily i.m. injections of either 5 micrograms or 0.5 micrograms ICI 118630 in saline were as effective as ovariectomy or tamoxifen therapy in causing the regression of ER+ DMBA-induced mammary tumours. ER- mammary tumours showed a more equivocal overall response to ICI 118630, some tumours progressing, others regressing. About one-third of the ER+ tumours disappeared in the 20-day treatment period. Those tumours which did regrow after the cessation of treatment proved to be hormone-dependent. In addition to the inhibitory effects of the LH-RH agonist on pre-existing tumours, ICI 118630 also reduced the total number of new tumours formed during and after treatment. 1979-03 /pmc/articles/PMC2009890/ /pubmed/380618 Text en
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Nicholson, R. I.
Maynard, P. V.
spellingShingle Nicholson, R. I.
Maynard, P. V.
Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist.
author_facet Nicholson, R. I.
Maynard, P. V.
author_sort Nicholson, R. I.
title Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist.
title_short Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist.
title_full Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist.
title_fullStr Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist.
title_full_unstemmed Anti-tumour activity of ICI 118630, a new potent luteinizing hormone-releasing hormone agonist.
title_sort anti-tumour activity of ici 118630, a new potent luteinizing hormone-releasing hormone agonist.
description Experiments were undertaken with DMBA-induced mammary tumours of the rat to determine the anti-tumour properties of a new and potent luteinizing hormone releasing hormone (LH-RH) agonist, [D-Ser(But) 6Azgly10]-LH-RH (ICI 118630). Tumours were classified according to their oestrogen-receptor (ER) content. Twice daily i.m. injections of either 5 micrograms or 0.5 micrograms ICI 118630 in saline were as effective as ovariectomy or tamoxifen therapy in causing the regression of ER+ DMBA-induced mammary tumours. ER- mammary tumours showed a more equivocal overall response to ICI 118630, some tumours progressing, others regressing. About one-third of the ER+ tumours disappeared in the 20-day treatment period. Those tumours which did regrow after the cessation of treatment proved to be hormone-dependent. In addition to the inhibitory effects of the LH-RH agonist on pre-existing tumours, ICI 118630 also reduced the total number of new tumours formed during and after treatment.
publishDate 1979
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009890/
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