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DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism

PURPOSE: Selenium, both essential and toxic element, is considered to protect against cancer, though human supplementation trials have generated many inconsistent data. Genetic background may partially explain a great variability of the studies related to selenium and human health. The aim of this s...

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Autores principales: Jablonska, E., Raimondi, S., Gromadzinska, J., Reszka, E., Wieczorek, E., Krol, M. B., Smok-Pieniazek, A., Nocun, M., Stepnik, M., Socha, K., Borawska, M. H., Wasowicz, W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122617/
https://www.ncbi.nlm.nih.gov/pubmed/26658762
http://dx.doi.org/10.1007/s00394-015-1118-4
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author Jablonska, E.
Raimondi, S.
Gromadzinska, J.
Reszka, E.
Wieczorek, E.
Krol, M. B.
Smok-Pieniazek, A.
Nocun, M.
Stepnik, M.
Socha, K.
Borawska, M. H.
Wasowicz, W.
author_facet Jablonska, E.
Raimondi, S.
Gromadzinska, J.
Reszka, E.
Wieczorek, E.
Krol, M. B.
Smok-Pieniazek, A.
Nocun, M.
Stepnik, M.
Socha, K.
Borawska, M. H.
Wasowicz, W.
author_sort Jablonska, E.
collection PubMed
description PURPOSE: Selenium, both essential and toxic element, is considered to protect against cancer, though human supplementation trials have generated many inconsistent data. Genetic background may partially explain a great variability of the studies related to selenium and human health. The aim of this study was to assess whether functional polymorphisms within two selenoprotein-encoding genes modify the response to selenium at the level of oxidative stress, DNA damage, and mRNA expression, especially in the individuals with a relatively low selenium status. METHODS: The trial involved 95 non-smoking individuals, stratified according to GPX1 rs1050450 and SEPP1 rs3877899 genotypes, and supplemented with selenium yeast (200 µg) for 6 weeks. Blood was collected at four time points, including 4 weeks of washout. RESULTS: After genotype stratification, the effect of GPX1 rs1050450 on lower GPx1 activity responsiveness was confirmed; however, in terms of DNA damage, we failed to indicate that individuals homozygous for variant allele may especially benefit from the increased selenium intake. Surprisingly, considering gene and time interaction, GPX1 polymorphism was observed to modify the level of DNA strand breaks during washout, showing a significant increase in GPX1 wild-type homozygotes. Regardless of the genotype, selenium supplementation was associated with a selectively suppressed selenoprotein mRNA expression and inconsistent changes in oxidative stress response, indicating for overlapped, antioxidant, and prooxidant effects. Intriguingly, DNA damage was not influenced by supplementation, but it was significantly increased during washout. CONCLUSIONS: These results point to an unclear relationship between selenium, genotype, and DNA damage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-015-1118-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-51226172016-12-09 DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism Jablonska, E. Raimondi, S. Gromadzinska, J. Reszka, E. Wieczorek, E. Krol, M. B. Smok-Pieniazek, A. Nocun, M. Stepnik, M. Socha, K. Borawska, M. H. Wasowicz, W. Eur J Nutr Original Contribution PURPOSE: Selenium, both essential and toxic element, is considered to protect against cancer, though human supplementation trials have generated many inconsistent data. Genetic background may partially explain a great variability of the studies related to selenium and human health. The aim of this study was to assess whether functional polymorphisms within two selenoprotein-encoding genes modify the response to selenium at the level of oxidative stress, DNA damage, and mRNA expression, especially in the individuals with a relatively low selenium status. METHODS: The trial involved 95 non-smoking individuals, stratified according to GPX1 rs1050450 and SEPP1 rs3877899 genotypes, and supplemented with selenium yeast (200 µg) for 6 weeks. Blood was collected at four time points, including 4 weeks of washout. RESULTS: After genotype stratification, the effect of GPX1 rs1050450 on lower GPx1 activity responsiveness was confirmed; however, in terms of DNA damage, we failed to indicate that individuals homozygous for variant allele may especially benefit from the increased selenium intake. Surprisingly, considering gene and time interaction, GPX1 polymorphism was observed to modify the level of DNA strand breaks during washout, showing a significant increase in GPX1 wild-type homozygotes. Regardless of the genotype, selenium supplementation was associated with a selectively suppressed selenoprotein mRNA expression and inconsistent changes in oxidative stress response, indicating for overlapped, antioxidant, and prooxidant effects. Intriguingly, DNA damage was not influenced by supplementation, but it was significantly increased during washout. CONCLUSIONS: These results point to an unclear relationship between selenium, genotype, and DNA damage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-015-1118-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-12-10 2016 /pmc/articles/PMC5122617/ /pubmed/26658762 http://dx.doi.org/10.1007/s00394-015-1118-4 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Contribution
Jablonska, E.
Raimondi, S.
Gromadzinska, J.
Reszka, E.
Wieczorek, E.
Krol, M. B.
Smok-Pieniazek, A.
Nocun, M.
Stepnik, M.
Socha, K.
Borawska, M. H.
Wasowicz, W.
DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism
title DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism
title_full DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism
title_fullStr DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism
title_full_unstemmed DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism
title_short DNA damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to GPX1 and SEPP1 polymorphism
title_sort dna damage and oxidative stress response to selenium yeast in the non-smoking individuals: a short-term supplementation trial with respect to gpx1 and sepp1 polymorphism
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122617/
https://www.ncbi.nlm.nih.gov/pubmed/26658762
http://dx.doi.org/10.1007/s00394-015-1118-4
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