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Control of cell proliferation in human glioma by glucocorticoids.
Survival and proliferation of cell cultures from human anaplastic astrocytomas were shown to be enhanced by glucocorticoids with an optimal concentration of approximately 2.5 x 10(-5)M (10 micrograms/ml). The stimulation of proliferation was only observed in a clonal growth assay and was reversed as...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1980
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010353/ https://www.ncbi.nlm.nih.gov/pubmed/7426310 |
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author | Freshney, R. I. Sherry, A. Hassanzadah, M. Freshney, M. Crilly, P. Morgan, D. |
author_facet | Freshney, R. I. Sherry, A. Hassanzadah, M. Freshney, M. Crilly, P. Morgan, D. |
author_sort | Freshney, R. I. |
collection | PubMed |
description | Survival and proliferation of cell cultures from human anaplastic astrocytomas were shown to be enhanced by glucocorticoids with an optimal concentration of approximately 2.5 x 10(-5)M (10 micrograms/ml). The stimulation of proliferation was only observed in a clonal growth assay and was reversed as the size of individual colonies reached approximately 50 cells. Above this size, and in regular monolayer cultures, glucocorticoids were found to inhibit cell proliferation as measured by direct cell counting and incorporation of [3H] thymidine. Cultures grown to maximum cell densities in non-limiting medium conditions reached a lower terminal cell density, and had a reduced labelling index with [3H] thymidine in the presence of glucocorticoids. Although there was little difference between the actions of beta-methasone, dexamethasone and ethyl prednisolone, methyl prednisolone was found to be more effective, both in terms of stimulation of clonal growth and inhibition of growth at high cell densities. There was no evidence of cytotoxicity with glucocorticoids up to 5 x 10(-5)M (20 micrograms/ml) and it is suggested that glucocorticoids act via a normal regulatory process, perhaps enhancing cell-cell recognition. IMAGES: |
format | Text |
id | pubmed-2010353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1980 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20103532009-09-10 Control of cell proliferation in human glioma by glucocorticoids. Freshney, R. I. Sherry, A. Hassanzadah, M. Freshney, M. Crilly, P. Morgan, D. Br J Cancer Research Article Survival and proliferation of cell cultures from human anaplastic astrocytomas were shown to be enhanced by glucocorticoids with an optimal concentration of approximately 2.5 x 10(-5)M (10 micrograms/ml). The stimulation of proliferation was only observed in a clonal growth assay and was reversed as the size of individual colonies reached approximately 50 cells. Above this size, and in regular monolayer cultures, glucocorticoids were found to inhibit cell proliferation as measured by direct cell counting and incorporation of [3H] thymidine. Cultures grown to maximum cell densities in non-limiting medium conditions reached a lower terminal cell density, and had a reduced labelling index with [3H] thymidine in the presence of glucocorticoids. Although there was little difference between the actions of beta-methasone, dexamethasone and ethyl prednisolone, methyl prednisolone was found to be more effective, both in terms of stimulation of clonal growth and inhibition of growth at high cell densities. There was no evidence of cytotoxicity with glucocorticoids up to 5 x 10(-5)M (20 micrograms/ml) and it is suggested that glucocorticoids act via a normal regulatory process, perhaps enhancing cell-cell recognition. IMAGES: Nature Publishing Group 1980-06 /pmc/articles/PMC2010353/ /pubmed/7426310 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 Freshney, R. I. Sherry, A. Hassanzadah, M. Freshney, M. Crilly, P. Morgan, D. Control of cell proliferation in human glioma by glucocorticoids. |
title | Control of cell proliferation in human glioma by glucocorticoids. |
title_full | Control of cell proliferation in human glioma by glucocorticoids. |
title_fullStr | Control of cell proliferation in human glioma by glucocorticoids. |
title_full_unstemmed | Control of cell proliferation in human glioma by glucocorticoids. |
title_short | Control of cell proliferation in human glioma by glucocorticoids. |
title_sort | control of cell proliferation in human glioma by glucocorticoids. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010353/ https://www.ncbi.nlm.nih.gov/pubmed/7426310 |
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