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31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.

We have shown by 31P-NMR spectroscopy that ovariectomy, in N-methyl-N-nitrosourea induced mammary adenocarcinomas, increases signals from phosphocreatine (PCr) relative to nucleoside triphosphate (NTP) before measurable regression (2 days) and for at least a further 13 days. The present study correl...

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Autores principales: Stubbs, M., Coombes, R. C., Griffiths, J. R., Maxwell, R. J., Rodrigues, L. M., Gusterson, B. A.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971421/
https://www.ncbi.nlm.nih.gov/pubmed/2310677
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author Stubbs, M.
Coombes, R. C.
Griffiths, J. R.
Maxwell, R. J.
Rodrigues, L. M.
Gusterson, B. A.
author_facet Stubbs, M.
Coombes, R. C.
Griffiths, J. R.
Maxwell, R. J.
Rodrigues, L. M.
Gusterson, B. A.
author_sort Stubbs, M.
collection PubMed
description We have shown by 31P-NMR spectroscopy that ovariectomy, in N-methyl-N-nitrosourea induced mammary adenocarcinomas, increases signals from phosphocreatine (PCr) relative to nucleoside triphosphate (NTP) before measurable regression (2 days) and for at least a further 13 days. The present study correlates the NMR changes with histological changes in the regressing tumour. Mammary tumours were examined by NMR before, and 2 and 14 days after, ovariectomy or sham-ovariectomy. Sections were taken from five tumours at each time point after operation for histology and for immunocytochemical staining of myoepithelial cells, luminal cells and basement membrane material. The histology showed typical cribriform papillary type mammary adenocarcinomas. The luminal cell population had a high mitotic activity and there was a prominent myoepithelial layer. At 2 days post-ovariectomy no significant change in mitotic activity was observed and no cytological characteristics attributable to ovariectomy could be seen. At 14 days postovariectomy the tumour was indistinguishable from a tubular adenoma, had significantly reduced mitotic activity, a relative increase in myoepithelial cells and basement membrane material. The changes detected by NMR must reflect early metabolic events, perhaps related to the histological changes observed at 14 days after ovariectomy. 31P-NMR spectroscopy may permit early monitoring of endocrine therapy for mammary cancer. IMAGES:
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spelling pubmed-19714212009-09-10 31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy. Stubbs, M. Coombes, R. C. Griffiths, J. R. Maxwell, R. J. Rodrigues, L. M. Gusterson, B. A. Br J Cancer Research Article We have shown by 31P-NMR spectroscopy that ovariectomy, in N-methyl-N-nitrosourea induced mammary adenocarcinomas, increases signals from phosphocreatine (PCr) relative to nucleoside triphosphate (NTP) before measurable regression (2 days) and for at least a further 13 days. The present study correlates the NMR changes with histological changes in the regressing tumour. Mammary tumours were examined by NMR before, and 2 and 14 days after, ovariectomy or sham-ovariectomy. Sections were taken from five tumours at each time point after operation for histology and for immunocytochemical staining of myoepithelial cells, luminal cells and basement membrane material. The histology showed typical cribriform papillary type mammary adenocarcinomas. The luminal cell population had a high mitotic activity and there was a prominent myoepithelial layer. At 2 days post-ovariectomy no significant change in mitotic activity was observed and no cytological characteristics attributable to ovariectomy could be seen. At 14 days postovariectomy the tumour was indistinguishable from a tubular adenoma, had significantly reduced mitotic activity, a relative increase in myoepithelial cells and basement membrane material. The changes detected by NMR must reflect early metabolic events, perhaps related to the histological changes observed at 14 days after ovariectomy. 31P-NMR spectroscopy may permit early monitoring of endocrine therapy for mammary cancer. IMAGES: Nature Publishing Group 1990-02 /pmc/articles/PMC1971421/ /pubmed/2310677 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Stubbs, M.
Coombes, R. C.
Griffiths, J. R.
Maxwell, R. J.
Rodrigues, L. M.
Gusterson, B. A.
31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.
title 31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.
title_full 31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.
title_fullStr 31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.
title_full_unstemmed 31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.
title_short 31P-NMR spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.
title_sort 31p-nmr spectroscopy and histological studies of the response of rat mammary tumours to endocrine therapy.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971421/
https://www.ncbi.nlm.nih.gov/pubmed/2310677
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