Cargando…

A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo.

The hypoxic cell radiosensitizing properties of nimorazole have been investigated in a C3H mammary carcinoma transplanted to the feet of C3D2F1. The results have been compared with those obtained with misonidazole (MISO) in the same animal tumour system. For single-dose irradiation in air, nimorazol...

Descripción completa

Detalles Bibliográficos
Autores principales: Overgaard, J., Overgaard, M., Nielsen, O. S., Pedersen, A. K., Timothy, A. R.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1982
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011219/
https://www.ncbi.nlm.nih.gov/pubmed/7150484
_version_ 1782136485764399104
author Overgaard, J.
Overgaard, M.
Nielsen, O. S.
Pedersen, A. K.
Timothy, A. R.
author_facet Overgaard, J.
Overgaard, M.
Nielsen, O. S.
Pedersen, A. K.
Timothy, A. R.
author_sort Overgaard, J.
collection PubMed
description The hypoxic cell radiosensitizing properties of nimorazole have been investigated in a C3H mammary carcinoma transplanted to the feet of C3D2F1. The results have been compared with those obtained with misonidazole (MISO) in the same animal tumour system. For single-dose irradiation in air, nimorazole gives an enhancement ratio (ER) of approximately 1.4, independent of the dose of drug administered over the range 0.1-1.0 mg/g. MISO yields a similar ER at the 0.1 mg/g level but, unlike nimorazole, shows a steep dose-response curve with an ER of 2.2 when given in a concentration of 1.0 mg/g. No such dose-response relationship is seen with nimorazole despite the fact that tumour and plasma concentrations of the 2 drugs have an identical dose relationship. With irradiation given in 5 daily fractions, nimorazole and MISO at a dose of 0.3 mg/g per fraction both show an ER of approximately 1.3. The high drug doses used in single-fraction radiation experiments in animals bear little relation to those applicable to clinical practice since these would result in unacceptable toxicity. The results of the present studies are therefore of interest as nimorazole is potentially less toxic than MISO in humans but demonstrates similar radiosensitizing properties at clinically relevant dose levels.
format Text
id pubmed-2011219
institution National Center for Biotechnology Information
language English
publishDate 1982
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-20112192009-09-10 A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo. Overgaard, J. Overgaard, M. Nielsen, O. S. Pedersen, A. K. Timothy, A. R. Br J Cancer Research Article The hypoxic cell radiosensitizing properties of nimorazole have been investigated in a C3H mammary carcinoma transplanted to the feet of C3D2F1. The results have been compared with those obtained with misonidazole (MISO) in the same animal tumour system. For single-dose irradiation in air, nimorazole gives an enhancement ratio (ER) of approximately 1.4, independent of the dose of drug administered over the range 0.1-1.0 mg/g. MISO yields a similar ER at the 0.1 mg/g level but, unlike nimorazole, shows a steep dose-response curve with an ER of 2.2 when given in a concentration of 1.0 mg/g. No such dose-response relationship is seen with nimorazole despite the fact that tumour and plasma concentrations of the 2 drugs have an identical dose relationship. With irradiation given in 5 daily fractions, nimorazole and MISO at a dose of 0.3 mg/g per fraction both show an ER of approximately 1.3. The high drug doses used in single-fraction radiation experiments in animals bear little relation to those applicable to clinical practice since these would result in unacceptable toxicity. The results of the present studies are therefore of interest as nimorazole is potentially less toxic than MISO in humans but demonstrates similar radiosensitizing properties at clinically relevant dose levels. Nature Publishing Group 1982-12 /pmc/articles/PMC2011219/ /pubmed/7150484 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
Overgaard, J.
Overgaard, M.
Nielsen, O. S.
Pedersen, A. K.
Timothy, A. R.
A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo.
title A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo.
title_full A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo.
title_fullStr A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo.
title_full_unstemmed A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo.
title_short A comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a C3H mammary carcinoma in vivo.
title_sort comparative investigation of nimorazole and misonidazole as hypoxic radiosensitizers in a c3h mammary carcinoma in vivo.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011219/
https://www.ncbi.nlm.nih.gov/pubmed/7150484
work_keys_str_mv AT overgaardj acomparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT overgaardm acomparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT nielsenos acomparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT pedersenak acomparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT timothyar acomparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT overgaardj comparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT overgaardm comparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT nielsenos comparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT pedersenak comparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo
AT timothyar comparativeinvestigationofnimorazoleandmisonidazoleashypoxicradiosensitizersinac3hmammarycarcinomainvivo