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Release from the Crabtree effect by hypoxic cell radiosensitizers.

The Crabtree effect can be observed when the O2 consumption of tumour cells or of mammalian cells grown in culture is measured in physiological medium containing glucose. The effect of 2 hypoxic cell radiosensitizers, misonidazole and NDPP, on the O2 consumption of Ehrlich ascites tumour cells was c...

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Detalles Bibliográficos
Autores principales: Mustea, I., Bara, A.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1979
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010000/
https://www.ncbi.nlm.nih.gov/pubmed/475972
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author Mustea, I.
Bara, A.
author_facet Mustea, I.
Bara, A.
author_sort Mustea, I.
collection PubMed
description The Crabtree effect can be observed when the O2 consumption of tumour cells or of mammalian cells grown in culture is measured in physiological medium containing glucose. The effect of 2 hypoxic cell radiosensitizers, misonidazole and NDPP, on the O2 consumption of Ehrlich ascites tumour cells was compared in media with and without glucose. A stimulatory effect on O2 consumption was found for 5--20mM misonidazole as well as for 0.5mM NDPP, both in media containing 10(-2)M glucose. Thus glucose induced a Crabtree effect in Ehrlich tumour cells, expressed as 38--45% inhibition of O2 consumption relative to that in the same medium without glucose. The stimulatory effect of misonidazole and NDPP on O2 utilization in medium with glucose undoubtedly appeared as a release from the Crabtree effect.
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spelling pubmed-20100002009-09-10 Release from the Crabtree effect by hypoxic cell radiosensitizers. Mustea, I. Bara, A. Br J Cancer Research Article The Crabtree effect can be observed when the O2 consumption of tumour cells or of mammalian cells grown in culture is measured in physiological medium containing glucose. The effect of 2 hypoxic cell radiosensitizers, misonidazole and NDPP, on the O2 consumption of Ehrlich ascites tumour cells was compared in media with and without glucose. A stimulatory effect on O2 consumption was found for 5--20mM misonidazole as well as for 0.5mM NDPP, both in media containing 10(-2)M glucose. Thus glucose induced a Crabtree effect in Ehrlich tumour cells, expressed as 38--45% inhibition of O2 consumption relative to that in the same medium without glucose. The stimulatory effect of misonidazole and NDPP on O2 utilization in medium with glucose undoubtedly appeared as a release from the Crabtree effect. Nature Publishing Group 1979-08 /pmc/articles/PMC2010000/ /pubmed/475972 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
Mustea, I.
Bara, A.
Release from the Crabtree effect by hypoxic cell radiosensitizers.
title Release from the Crabtree effect by hypoxic cell radiosensitizers.
title_full Release from the Crabtree effect by hypoxic cell radiosensitizers.
title_fullStr Release from the Crabtree effect by hypoxic cell radiosensitizers.
title_full_unstemmed Release from the Crabtree effect by hypoxic cell radiosensitizers.
title_short Release from the Crabtree effect by hypoxic cell radiosensitizers.
title_sort release from the crabtree effect by hypoxic cell radiosensitizers.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010000/
https://www.ncbi.nlm.nih.gov/pubmed/475972
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