Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats.

The 32P uptake in a mammary tumour induced by DMBA and in the Walker 256 carcinosarcoma was measured by external GM -tubes. The uptake was significantly higher than in the skin. During exposure to a synchronized light regime a circadian variation was present in the 32P uptake of the hormone-dependen...

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Autores principales: Møoller, U., Bojsen, J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1976
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2025109/
https://www.ncbi.nlm.nih.gov/pubmed/820364
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author Møoller, U.
Bojsen, J.
author_facet Møoller, U.
Bojsen, J.
author_sort Møoller, U.
collection PubMed
description The 32P uptake in a mammary tumour induced by DMBA and in the Walker 256 carcinosarcoma was measured by external GM -tubes. The uptake was significantly higher than in the skin. During exposure to a synchronized light regime a circadian variation was present in the 32P uptake of the hormone-dependent DMBA-induced tumour. The maximal 32P uptake was in the dark period, in which the highest temperature in the tumour has also been found (Møoller and Bojsen, 1975). In the hormone-independent Walker 256 carcinosarcoma there was no periodicity in 32P uptake. No variation in 32P uptake was registered in the skin of normal controls or in tumour-bearing rats.
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spelling pubmed-20251092009-09-10 Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats. Møoller, U. Bojsen, J. Br J Cancer Research Article The 32P uptake in a mammary tumour induced by DMBA and in the Walker 256 carcinosarcoma was measured by external GM -tubes. The uptake was significantly higher than in the skin. During exposure to a synchronized light regime a circadian variation was present in the 32P uptake of the hormone-dependent DMBA-induced tumour. The maximal 32P uptake was in the dark period, in which the highest temperature in the tumour has also been found (Møoller and Bojsen, 1975). In the hormone-independent Walker 256 carcinosarcoma there was no periodicity in 32P uptake. No variation in 32P uptake was registered in the skin of normal controls or in tumour-bearing rats. Nature Publishing Group 1976-06 /pmc/articles/PMC2025109/ /pubmed/820364 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
Møoller, U.
Bojsen, J.
Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats.
title Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats.
title_full Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats.
title_fullStr Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats.
title_full_unstemmed Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats.
title_short Circadian variations in 32P uptake of DMBA-induced mammary tumour and Walker carcinosarcoma in rats.
title_sort circadian variations in 32p uptake of dmba-induced mammary tumour and walker carcinosarcoma in rats.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2025109/
https://www.ncbi.nlm.nih.gov/pubmed/820364
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