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Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts
A double staining technique was developed for the simultaneous measurement of tissue hypoxia and the concentration of non-protein sulphydryls (NPSH), based on the fluorinated nitroimidazole EF5 and the fluorescent histochemical NPSH stain 1-(4-chloromercuriphenoylazo)-naphthol-2 (mercury orange). Cr...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1999
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362959/ https://www.ncbi.nlm.nih.gov/pubmed/10576655 http://dx.doi.org/10.1038/sj.bjc.6690797 |
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author | Moreno-Merlo, F Nicklee, T Hedley, D W |
author_facet | Moreno-Merlo, F Nicklee, T Hedley, D W |
author_sort | Moreno-Merlo, F |
collection | PubMed |
description | A double staining technique was developed for the simultaneous measurement of tissue hypoxia and the concentration of non-protein sulphydryls (NPSH), based on the fluorinated nitroimidazole EF5 and the fluorescent histochemical NPSH stain 1-(4-chloromercuriphenoylazo)-naphthol-2 (mercury orange). Cryostat sections of tumour tissue were examined by fluorescence image analysis, using a computer-controlled microscope stage to generate large tiled field images of the cut tumour surface. This method was applied to the human cervical squamous cell carcinoma lines ME180 and SiHa, grown as xenografts in severe combined immunodeficient (SCID) mice, in order to determine if there is a systematic relationship between tissue hypoxia and NPSH levels. Hypoxic regions of the tumours, defined by EF5 labelling, were found to show greater NPSH concentrations relative to better oxygenated regions. This is probably due to increases in glutathione, since the ME180 and SiHa xenografts contained low levels of cysteine and metallothionein; the other major cellular thiols that can bind to mercury orange. Because the effects of glutathione on radiation and chemotherapy resistance are likely to be greater under hypoxic conditions, these results have potentially important implications for the study of resistance mechanisms in solid tumours. © 1999 Cancer Research Campaign |
format | Text |
id | pubmed-2362959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23629592009-09-10 Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts Moreno-Merlo, F Nicklee, T Hedley, D W Br J Cancer Regular Article A double staining technique was developed for the simultaneous measurement of tissue hypoxia and the concentration of non-protein sulphydryls (NPSH), based on the fluorinated nitroimidazole EF5 and the fluorescent histochemical NPSH stain 1-(4-chloromercuriphenoylazo)-naphthol-2 (mercury orange). Cryostat sections of tumour tissue were examined by fluorescence image analysis, using a computer-controlled microscope stage to generate large tiled field images of the cut tumour surface. This method was applied to the human cervical squamous cell carcinoma lines ME180 and SiHa, grown as xenografts in severe combined immunodeficient (SCID) mice, in order to determine if there is a systematic relationship between tissue hypoxia and NPSH levels. Hypoxic regions of the tumours, defined by EF5 labelling, were found to show greater NPSH concentrations relative to better oxygenated regions. This is probably due to increases in glutathione, since the ME180 and SiHa xenografts contained low levels of cysteine and metallothionein; the other major cellular thiols that can bind to mercury orange. Because the effects of glutathione on radiation and chemotherapy resistance are likely to be greater under hypoxic conditions, these results have potentially important implications for the study of resistance mechanisms in solid tumours. © 1999 Cancer Research Campaign Nature Publishing Group 1999-11 /pmc/articles/PMC2362959/ /pubmed/10576655 http://dx.doi.org/10.1038/sj.bjc.6690797 Text en Copyright © 1999 Cancer Research Campaign 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 | Regular Article Moreno-Merlo, F Nicklee, T Hedley, D W Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts |
title | Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts |
title_full | Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts |
title_fullStr | Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts |
title_full_unstemmed | Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts |
title_short | Association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts |
title_sort | association between tissue hypoxia and elevated non-protein sulphydryl concentrations in human cervical carcinoma xenografts |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362959/ https://www.ncbi.nlm.nih.gov/pubmed/10576655 http://dx.doi.org/10.1038/sj.bjc.6690797 |
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