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Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity.
The radiation response of 5 different lines of human melanoma xenografts was studied. Tumours grown s.c. in the flanks of athymic mice were exposed to single doses of 5-25 Gy and subsequently analysed with respect to specific growth delay. The variation in radiation response among these melanoma lin...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1985
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977029/ https://www.ncbi.nlm.nih.gov/pubmed/3966977 |
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author | Rofstad, E. K. Brustad, T. |
author_facet | Rofstad, E. K. Brustad, T. |
author_sort | Rofstad, E. K. |
collection | PubMed |
description | The radiation response of 5 different lines of human melanoma xenografts was studied. Tumours grown s.c. in the flanks of athymic mice were exposed to single doses of 5-25 Gy and subsequently analysed with respect to specific growth delay. The variation in radiation response among these melanoma lines was almost as large as that reported for human tumour xenografts differing in histological type. The most radioresistant melanomas showed longer volume-doubling times, lower growth fractions, higher cell loss factors and lower vascular density than the most radiosensitive ones. The radiation response was not correlated to the fraction of cells in S-phase or the DNA content of the tumour cells. Cell suspensions prepared from the different melanomas, irradiated under aerobic conditions and assayed in soft agar, also showed large variability in radiation response. Specific growth delay after 15 Gy was found to be correlated to the surviving fraction measured in vitro after 6 Gy, but not clearly to the Do value. It is suggested that tumour growth characteristics in vivo as well as radiation response in vitro may be of prognostic value for prediction of radioresponsiveness of melanomas. |
format | Text |
id | pubmed-1977029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1985 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19770292009-09-10 Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. Rofstad, E. K. Brustad, T. Br J Cancer Research Article The radiation response of 5 different lines of human melanoma xenografts was studied. Tumours grown s.c. in the flanks of athymic mice were exposed to single doses of 5-25 Gy and subsequently analysed with respect to specific growth delay. The variation in radiation response among these melanoma lines was almost as large as that reported for human tumour xenografts differing in histological type. The most radioresistant melanomas showed longer volume-doubling times, lower growth fractions, higher cell loss factors and lower vascular density than the most radiosensitive ones. The radiation response was not correlated to the fraction of cells in S-phase or the DNA content of the tumour cells. Cell suspensions prepared from the different melanomas, irradiated under aerobic conditions and assayed in soft agar, also showed large variability in radiation response. Specific growth delay after 15 Gy was found to be correlated to the surviving fraction measured in vitro after 6 Gy, but not clearly to the Do value. It is suggested that tumour growth characteristics in vivo as well as radiation response in vitro may be of prognostic value for prediction of radioresponsiveness of melanomas. Nature Publishing Group 1985-02 /pmc/articles/PMC1977029/ /pubmed/3966977 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 Rofstad, E. K. Brustad, T. Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. |
title | Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. |
title_full | Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. |
title_fullStr | Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. |
title_full_unstemmed | Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. |
title_short | Tumour growth delay following single dose irradiation of human melanoma xenografts. Correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. |
title_sort | tumour growth delay following single dose irradiation of human melanoma xenografts. correlations with tumour growth parameters, vascular structure and cellular radiosensitivity. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977029/ https://www.ncbi.nlm.nih.gov/pubmed/3966977 |
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