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Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice
The present study investigated the effects of breast tumors on the blood and tissue distribution of essential trace mineral selenium (Se), and oxidative stress status of mice. Female 10-week-old BALB/cByJNarl mice were randomly assigned into control (CNL) and breast tumor-bearing (TB) groups. TB mic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635215/ https://www.ncbi.nlm.nih.gov/pubmed/23429470 http://dx.doi.org/10.3390/nu5020594 |
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author | Guo, Chih-Hung Hsia, Simon Chen, Pei-Chung |
author_facet | Guo, Chih-Hung Hsia, Simon Chen, Pei-Chung |
author_sort | Guo, Chih-Hung |
collection | PubMed |
description | The present study investigated the effects of breast tumors on the blood and tissue distribution of essential trace mineral selenium (Se), and oxidative stress status of mice. Female 10-week-old BALB/cByJNarl mice were randomly assigned into control (CNL) and breast tumor-bearing (TB) groups. TB mice were injected subcutaneously into the right hind thigh with 5 × 10(6) EMT6 mouse mammary tumor cells. After 22 days, we measured Se concentrations, Se-dependent glutathione peroxidase (GPx) activities, and malondialdehyde (MDA) products (indicator of oxidative stress) in plasma, various tissues, and plasma vascular endothelial growth factor (VEGF) concentrations. There were no significant differences in body weights and daily intake between both groups. Compared with the CNL group, TB mice have decreases in plasma Se concentrations and GPx activities, as well as higher plasma VEGF and MDA concentrations. Plasma Se concentrations were also negatively correlated with plasma MDA and VEGF concentrations. Furthermore, tissue Se concentrations and GPx activities in TB animals were lower; whereas the MDA concentrations higher in various tissues including liver, kidney, brain, lung, spleen, and thymic tissues. In conclusion, disruption of Se homeostasis critically reflects oxidative stress in target tissues, thus may increase the risk for progression of breast cancer and metastasis. |
format | Online Article Text |
id | pubmed-3635215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-36352152013-05-02 Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice Guo, Chih-Hung Hsia, Simon Chen, Pei-Chung Nutrients Article The present study investigated the effects of breast tumors on the blood and tissue distribution of essential trace mineral selenium (Se), and oxidative stress status of mice. Female 10-week-old BALB/cByJNarl mice were randomly assigned into control (CNL) and breast tumor-bearing (TB) groups. TB mice were injected subcutaneously into the right hind thigh with 5 × 10(6) EMT6 mouse mammary tumor cells. After 22 days, we measured Se concentrations, Se-dependent glutathione peroxidase (GPx) activities, and malondialdehyde (MDA) products (indicator of oxidative stress) in plasma, various tissues, and plasma vascular endothelial growth factor (VEGF) concentrations. There were no significant differences in body weights and daily intake between both groups. Compared with the CNL group, TB mice have decreases in plasma Se concentrations and GPx activities, as well as higher plasma VEGF and MDA concentrations. Plasma Se concentrations were also negatively correlated with plasma MDA and VEGF concentrations. Furthermore, tissue Se concentrations and GPx activities in TB animals were lower; whereas the MDA concentrations higher in various tissues including liver, kidney, brain, lung, spleen, and thymic tissues. In conclusion, disruption of Se homeostasis critically reflects oxidative stress in target tissues, thus may increase the risk for progression of breast cancer and metastasis. MDPI 2013-02-20 /pmc/articles/PMC3635215/ /pubmed/23429470 http://dx.doi.org/10.3390/nu5020594 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Guo, Chih-Hung Hsia, Simon Chen, Pei-Chung Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice |
title | Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice |
title_full | Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice |
title_fullStr | Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice |
title_full_unstemmed | Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice |
title_short | Distribution of Selenium and Oxidative Stress in Breast Tumor-Bearing Mice |
title_sort | distribution of selenium and oxidative stress in breast tumor-bearing mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3635215/ https://www.ncbi.nlm.nih.gov/pubmed/23429470 http://dx.doi.org/10.3390/nu5020594 |
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