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Enhancement of the effect of cytotoxic drugs by radiosensitizers.

Misonidazole (MISO) potentiates the action of cyclophosphamide (CY) and melphalan in the WHFIB culture-adapted fibrosarcoma, whether assayed by cell survival or tumour-growth delay. In the case of CY, MISO also inhibited recovery from potentially lethal drug damage. The optimum effect was seen when...

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Detalles Bibliográficos
Autores principales: Martin, W. M., McNally, N. J., De Ronde, J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010716/
https://www.ncbi.nlm.nih.gov/pubmed/7248157
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author Martin, W. M.
McNally, N. J.
De Ronde, J.
author_facet Martin, W. M.
McNally, N. J.
De Ronde, J.
author_sort Martin, W. M.
collection PubMed
description Misonidazole (MISO) potentiates the action of cyclophosphamide (CY) and melphalan in the WHFIB culture-adapted fibrosarcoma, whether assayed by cell survival or tumour-growth delay. In the case of CY, MISO also inhibited recovery from potentially lethal drug damage. The optimum effect was seen when MISO was given 1 h before CY, though it was also effective when given 6 h before or 1 h after the drug. Other radiosensitizers also potentiated the action of CY. There was only a small effect of MISO on the LD50 of CY and no effect on CY toxicity as assayed by changes in blood counts or damage to bladder epithelium. However, mice bearing multiple lung tumours were less able to cope with the combined treatment than those bearing s.c. tumours.
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spelling pubmed-20107162009-09-10 Enhancement of the effect of cytotoxic drugs by radiosensitizers. Martin, W. M. McNally, N. J. De Ronde, J. Br J Cancer Research Article Misonidazole (MISO) potentiates the action of cyclophosphamide (CY) and melphalan in the WHFIB culture-adapted fibrosarcoma, whether assayed by cell survival or tumour-growth delay. In the case of CY, MISO also inhibited recovery from potentially lethal drug damage. The optimum effect was seen when MISO was given 1 h before CY, though it was also effective when given 6 h before or 1 h after the drug. Other radiosensitizers also potentiated the action of CY. There was only a small effect of MISO on the LD50 of CY and no effect on CY toxicity as assayed by changes in blood counts or damage to bladder epithelium. However, mice bearing multiple lung tumours were less able to cope with the combined treatment than those bearing s.c. tumours. Nature Publishing Group 1981-06 /pmc/articles/PMC2010716/ /pubmed/7248157 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
Martin, W. M.
McNally, N. J.
De Ronde, J.
Enhancement of the effect of cytotoxic drugs by radiosensitizers.
title Enhancement of the effect of cytotoxic drugs by radiosensitizers.
title_full Enhancement of the effect of cytotoxic drugs by radiosensitizers.
title_fullStr Enhancement of the effect of cytotoxic drugs by radiosensitizers.
title_full_unstemmed Enhancement of the effect of cytotoxic drugs by radiosensitizers.
title_short Enhancement of the effect of cytotoxic drugs by radiosensitizers.
title_sort enhancement of the effect of cytotoxic drugs by radiosensitizers.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010716/
https://www.ncbi.nlm.nih.gov/pubmed/7248157
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