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Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA

Trace element selenium (Se) is regarded to be a breast cancer preventive factor involved in multiple protective pathways. In all, 80 women with breast cancer who underwent a radical mastectomy were enrolled in the study. Serum Se and carcinoembryonic antigen levels were measured using a fluorometric...

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Autores principales: Charalabopoulos, K, Kotsalos, A, Batistatou, A, Charalabopoulos, A, Vezyraki, P, Peschos, D, Kalfakakou, V, Evangelou, A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360505/
https://www.ncbi.nlm.nih.gov/pubmed/16880784
http://dx.doi.org/10.1038/sj.bjc.6603292
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author Charalabopoulos, K
Kotsalos, A
Batistatou, A
Charalabopoulos, A
Vezyraki, P
Peschos, D
Kalfakakou, V
Evangelou, A
author_facet Charalabopoulos, K
Kotsalos, A
Batistatou, A
Charalabopoulos, A
Vezyraki, P
Peschos, D
Kalfakakou, V
Evangelou, A
author_sort Charalabopoulos, K
collection PubMed
description Trace element selenium (Se) is regarded to be a breast cancer preventive factor involved in multiple protective pathways. In all, 80 women with breast cancer who underwent a radical mastectomy were enrolled in the study. Serum Se and carcinoembryonic antigen levels were measured using a fluorometric and IRMA assay, respectively. Se tissue concentration was determined by a tissue extracting fluorometric assay. For statistical analysis purposes t-test was used and P-values <0.001 were regarded as statistically significant. Serum Se was 42.5±7.5 μg l(−1) in breast cancer patients and 67.6±5.36 μg l(−1) in the age-matched control group of healthy individuals. Serum carcinoembryonic antigen in patients was 10±1.7 U ml(−1) (normal <2.5 U ml(−1) in nonsmokers/<3.5 U ml(−1) in smokers). A statistically significant difference was found for both serum Se and CEA between two groups studied (P<0.001). Neoplastic tissue Se concentration was 2660±210 mg g(−1) tissue; its concentration in the adjacent non-neoplastic tissue was 680±110 mg g(−1) tissue (P<0.001). An inverse relationship between Se and CEA serum levels was found in the two groups studied (r=−0.794). There was no correlation between serum/tissue Se concentration and stage of the disease. The decrease in serum Se concentration as well as its increased concentration in the neoplastic breast tissue is of great significance. These alterations may reflect part of the defence mechanisms against the carcinogenetic process.
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spelling pubmed-23605052009-09-10 Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA Charalabopoulos, K Kotsalos, A Batistatou, A Charalabopoulos, A Vezyraki, P Peschos, D Kalfakakou, V Evangelou, A Br J Cancer Clinical Study Trace element selenium (Se) is regarded to be a breast cancer preventive factor involved in multiple protective pathways. In all, 80 women with breast cancer who underwent a radical mastectomy were enrolled in the study. Serum Se and carcinoembryonic antigen levels were measured using a fluorometric and IRMA assay, respectively. Se tissue concentration was determined by a tissue extracting fluorometric assay. For statistical analysis purposes t-test was used and P-values <0.001 were regarded as statistically significant. Serum Se was 42.5±7.5 μg l(−1) in breast cancer patients and 67.6±5.36 μg l(−1) in the age-matched control group of healthy individuals. Serum carcinoembryonic antigen in patients was 10±1.7 U ml(−1) (normal <2.5 U ml(−1) in nonsmokers/<3.5 U ml(−1) in smokers). A statistically significant difference was found for both serum Se and CEA between two groups studied (P<0.001). Neoplastic tissue Se concentration was 2660±210 mg g(−1) tissue; its concentration in the adjacent non-neoplastic tissue was 680±110 mg g(−1) tissue (P<0.001). An inverse relationship between Se and CEA serum levels was found in the two groups studied (r=−0.794). There was no correlation between serum/tissue Se concentration and stage of the disease. The decrease in serum Se concentration as well as its increased concentration in the neoplastic breast tissue is of great significance. These alterations may reflect part of the defence mechanisms against the carcinogenetic process. Nature Publishing Group 2006-09-18 2006-08-01 /pmc/articles/PMC2360505/ /pubmed/16880784 http://dx.doi.org/10.1038/sj.bjc.6603292 Text en Copyright © 2006 Cancer Research UK 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 Clinical Study
Charalabopoulos, K
Kotsalos, A
Batistatou, A
Charalabopoulos, A
Vezyraki, P
Peschos, D
Kalfakakou, V
Evangelou, A
Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA
title Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA
title_full Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA
title_fullStr Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA
title_full_unstemmed Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA
title_short Selenium in serum and neoplastic tissue in breast cancer: correlation with CEA
title_sort selenium in serum and neoplastic tissue in breast cancer: correlation with cea
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360505/
https://www.ncbi.nlm.nih.gov/pubmed/16880784
http://dx.doi.org/10.1038/sj.bjc.6603292
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