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Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes
Growing evidence shows that improper intake of vitamin B6 increases cancer risk and several studies indicate that diabetic patients have a higher risk of developing tumors. We previously demonstrated that in Drosophila the deficiency of Pyridoxal 5′ phosphate (PLP), the active form of vitamin B6, ca...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065437/ https://www.ncbi.nlm.nih.gov/pubmed/30061626 http://dx.doi.org/10.1038/s41598-018-29801-z |
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author | Merigliano, Chiara Mascolo, Elisa La Torre, Mattia Saggio, Isabella Vernì, Fiammetta |
author_facet | Merigliano, Chiara Mascolo, Elisa La Torre, Mattia Saggio, Isabella Vernì, Fiammetta |
author_sort | Merigliano, Chiara |
collection | PubMed |
description | Growing evidence shows that improper intake of vitamin B6 increases cancer risk and several studies indicate that diabetic patients have a higher risk of developing tumors. We previously demonstrated that in Drosophila the deficiency of Pyridoxal 5′ phosphate (PLP), the active form of vitamin B6, causes chromosome aberrations (CABs), one of cancer prerequisites, and increases hemolymph glucose content. Starting from these data we asked if it was possible to provide a link between the aforementioned studies. Thus, we tested the effect of low PLP levels on DNA integrity in diabetic cells. To this aim we generated two Drosophila models of type 2 diabetes, the first by impairing insulin signaling and the second by rearing flies in high sugar diet. We showed that glucose treatment induced CABs in diabetic individuals but not in controls. More interestingly, PLP deficiency caused high frequencies of CABs in both diabetic models demonstrating that hyperglycemia, combined to reduced PLP level, impairs DNA integrity. PLP-depleted diabetic cells accumulated Advanced Glycation End products (AGEs) that largely contribute to CABs as α-lipoic acid, an AGE inhibitor, rescued not only AGEs but also CABs. These data, extrapolated to humans, indicate that low PLP levels, impacting on DNA integrity, may be considered one of the possible links between diabetes and cancer. |
format | Online Article Text |
id | pubmed-6065437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60654372018-08-06 Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes Merigliano, Chiara Mascolo, Elisa La Torre, Mattia Saggio, Isabella Vernì, Fiammetta Sci Rep Article Growing evidence shows that improper intake of vitamin B6 increases cancer risk and several studies indicate that diabetic patients have a higher risk of developing tumors. We previously demonstrated that in Drosophila the deficiency of Pyridoxal 5′ phosphate (PLP), the active form of vitamin B6, causes chromosome aberrations (CABs), one of cancer prerequisites, and increases hemolymph glucose content. Starting from these data we asked if it was possible to provide a link between the aforementioned studies. Thus, we tested the effect of low PLP levels on DNA integrity in diabetic cells. To this aim we generated two Drosophila models of type 2 diabetes, the first by impairing insulin signaling and the second by rearing flies in high sugar diet. We showed that glucose treatment induced CABs in diabetic individuals but not in controls. More interestingly, PLP deficiency caused high frequencies of CABs in both diabetic models demonstrating that hyperglycemia, combined to reduced PLP level, impairs DNA integrity. PLP-depleted diabetic cells accumulated Advanced Glycation End products (AGEs) that largely contribute to CABs as α-lipoic acid, an AGE inhibitor, rescued not only AGEs but also CABs. These data, extrapolated to humans, indicate that low PLP levels, impacting on DNA integrity, may be considered one of the possible links between diabetes and cancer. Nature Publishing Group UK 2018-07-30 /pmc/articles/PMC6065437/ /pubmed/30061626 http://dx.doi.org/10.1038/s41598-018-29801-z Text en © The Author(s) 2018 Open Access 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 http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Merigliano, Chiara Mascolo, Elisa La Torre, Mattia Saggio, Isabella Vernì, Fiammetta Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes |
title | Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes |
title_full | Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes |
title_fullStr | Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes |
title_full_unstemmed | Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes |
title_short | Protective role of vitamin B6 (PLP) against DNA damage in Drosophila models of type 2 diabetes |
title_sort | protective role of vitamin b6 (plp) against dna damage in drosophila models of type 2 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065437/ https://www.ncbi.nlm.nih.gov/pubmed/30061626 http://dx.doi.org/10.1038/s41598-018-29801-z |
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