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Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle.
The effect of dietary copper deficiency on tumour growth, neovascularisation and microvascular integrity was studied in the rat cremaster muscle. Male, weanling Sprague-Dawley rats were fed purified diets which were copper deficient (< 0.5 micrograms g-1 of diet) or copper adequate (5 micrograms...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1992
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978058/ https://www.ncbi.nlm.nih.gov/pubmed/1280989 |
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author | Schuschke, D. A. Reed, M. W. Saari, J. T. Olson, M. D. Ackermann, D. M. Miller, F. N. |
author_facet | Schuschke, D. A. Reed, M. W. Saari, J. T. Olson, M. D. Ackermann, D. M. Miller, F. N. |
author_sort | Schuschke, D. A. |
collection | PubMed |
description | The effect of dietary copper deficiency on tumour growth, neovascularisation and microvascular integrity was studied in the rat cremaster muscle. Male, weanling Sprague-Dawley rats were fed purified diets which were copper deficient (< 0.5 micrograms g-1 of diet) or copper adequate (5 micrograms g-1 of diet). Seven days after initiation of diets, a chondrosarcoma was implanted in the cremaster muscle of each rat. Five, 10 or 20 days after tumour implantation, rats were anesthetised and their cremasters prepared for observation by intravital microscopy. Intraarterial injection of fluorescein isothiocyanate-conjugated albumin and subsequent observation of fluorescence in the perivascular space indicated no difference in microvascular albumin leakage between the tumour vasculature of copper deficient and copper adequate rats. Neither tumour growth (assessed by wet weight), vascular density (assessed by light microscopy), nor any ultrastructural characteristics of the tumour or its vasculature (assessed by electron microscopy) were affected by copper deficiency. In view of findings by others which indicate changes in tumour characteristics with copper deficiency, we conclude that the copper dependency of tumour growth and vascularisation is a function of the type of tumour, the host tissue, or the conditions of copper depletion. |
format | Text |
id | pubmed-1978058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1992 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19780582009-09-10 Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. Schuschke, D. A. Reed, M. W. Saari, J. T. Olson, M. D. Ackermann, D. M. Miller, F. N. Br J Cancer Research Article The effect of dietary copper deficiency on tumour growth, neovascularisation and microvascular integrity was studied in the rat cremaster muscle. Male, weanling Sprague-Dawley rats were fed purified diets which were copper deficient (< 0.5 micrograms g-1 of diet) or copper adequate (5 micrograms g-1 of diet). Seven days after initiation of diets, a chondrosarcoma was implanted in the cremaster muscle of each rat. Five, 10 or 20 days after tumour implantation, rats were anesthetised and their cremasters prepared for observation by intravital microscopy. Intraarterial injection of fluorescein isothiocyanate-conjugated albumin and subsequent observation of fluorescence in the perivascular space indicated no difference in microvascular albumin leakage between the tumour vasculature of copper deficient and copper adequate rats. Neither tumour growth (assessed by wet weight), vascular density (assessed by light microscopy), nor any ultrastructural characteristics of the tumour or its vasculature (assessed by electron microscopy) were affected by copper deficiency. In view of findings by others which indicate changes in tumour characteristics with copper deficiency, we conclude that the copper dependency of tumour growth and vascularisation is a function of the type of tumour, the host tissue, or the conditions of copper depletion. Nature Publishing Group 1992-12 /pmc/articles/PMC1978058/ /pubmed/1280989 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 Schuschke, D. A. Reed, M. W. Saari, J. T. Olson, M. D. Ackermann, D. M. Miller, F. N. Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. |
title | Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. |
title_full | Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. |
title_fullStr | Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. |
title_full_unstemmed | Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. |
title_short | Short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. |
title_sort | short-term dietary copper deficiency does not inhibit angiogenesis in tumours implanted in striated muscle. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978058/ https://www.ncbi.nlm.nih.gov/pubmed/1280989 |
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