Cargando…
The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study
BACKGROUND: Reactive oxygen species may be involved in epigenetic gene activation or silencing. We aimed to identify CpG sites, at which DNA methylation is related to urinary 8-isoprostane levels (biomarker of lipid peroxidation) and cancer or mortality outcomes. This investigation was based on a Ge...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346508/ https://www.ncbi.nlm.nih.gov/pubmed/30678711 http://dx.doi.org/10.1186/s13148-018-0604-y |
_version_ | 1783389765685477376 |
---|---|
author | Gào, Xīn Zhang, Yan Burwinkel, Barbara Xuan, Yang Holleczek, Bernd Brenner, Hermann Schöttker, Ben |
author_facet | Gào, Xīn Zhang, Yan Burwinkel, Barbara Xuan, Yang Holleczek, Bernd Brenner, Hermann Schöttker, Ben |
author_sort | Gào, Xīn |
collection | PubMed |
description | BACKGROUND: Reactive oxygen species may be involved in epigenetic gene activation or silencing. We aimed to identify CpG sites, at which DNA methylation is related to urinary 8-isoprostane levels (biomarker of lipid peroxidation) and cancer or mortality outcomes. This investigation was based on a German, population-based cohort with linkage to cancer and mortality registry data (2000–2016). RESULTS: Blood DNA methylation in promoter regions of 519 genes, known to be involved in pathways from oxidative stress (OS) to cancer, was obtained at the cohort's baseline examination. Inverse associations of DNA methylation at cg25365794 (ALOXE3) and cg08862778 (MTOR) with 8-isoprostane levels were observed in a derivation set (n = 1000) and validated in two independent subsets of the cohort (n = 548 and n = 741). Multivariate regression models were used to evaluate the associations of DNA methylation at the two CpG sites with lung, colorectal, prostate, breast, and overall cancer incidence as well as CVD, cancer, and all-cause mortality. DNA methylation at cg25365794 (ALOXE3) was inversely associated with lung and prostate cancer incidence. DNA methylation at cg08862778 (MTOR) was associated with a 43% lower breast cancer incidence in the top vs. bottom tertile. CONCLUSION: The finding for ALOXE3 may not be causal. As ALOXE3 is mainly expressed in skin tissue, the observed association might reflect the fact that both DNA methylation at the ALOXE3 gene and urinary 8-isoprostane concentrations depend on the level of OS in tissues. Contrarily, the finding for the MTOR gene and breast cancer is biologically plausible because the MTOR protein plays an important role in PI3K/Akt signaling, which is a pathway related to cancer development and cell senescence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0604-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6346508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63465082019-01-29 The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study Gào, Xīn Zhang, Yan Burwinkel, Barbara Xuan, Yang Holleczek, Bernd Brenner, Hermann Schöttker, Ben Clin Epigenetics Research BACKGROUND: Reactive oxygen species may be involved in epigenetic gene activation or silencing. We aimed to identify CpG sites, at which DNA methylation is related to urinary 8-isoprostane levels (biomarker of lipid peroxidation) and cancer or mortality outcomes. This investigation was based on a German, population-based cohort with linkage to cancer and mortality registry data (2000–2016). RESULTS: Blood DNA methylation in promoter regions of 519 genes, known to be involved in pathways from oxidative stress (OS) to cancer, was obtained at the cohort's baseline examination. Inverse associations of DNA methylation at cg25365794 (ALOXE3) and cg08862778 (MTOR) with 8-isoprostane levels were observed in a derivation set (n = 1000) and validated in two independent subsets of the cohort (n = 548 and n = 741). Multivariate regression models were used to evaluate the associations of DNA methylation at the two CpG sites with lung, colorectal, prostate, breast, and overall cancer incidence as well as CVD, cancer, and all-cause mortality. DNA methylation at cg25365794 (ALOXE3) was inversely associated with lung and prostate cancer incidence. DNA methylation at cg08862778 (MTOR) was associated with a 43% lower breast cancer incidence in the top vs. bottom tertile. CONCLUSION: The finding for ALOXE3 may not be causal. As ALOXE3 is mainly expressed in skin tissue, the observed association might reflect the fact that both DNA methylation at the ALOXE3 gene and urinary 8-isoprostane concentrations depend on the level of OS in tissues. Contrarily, the finding for the MTOR gene and breast cancer is biologically plausible because the MTOR protein plays an important role in PI3K/Akt signaling, which is a pathway related to cancer development and cell senescence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0604-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-24 /pmc/articles/PMC6346508/ /pubmed/30678711 http://dx.doi.org/10.1186/s13148-018-0604-y Text en © The Author(s). 2019 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Gào, Xīn Zhang, Yan Burwinkel, Barbara Xuan, Yang Holleczek, Bernd Brenner, Hermann Schöttker, Ben The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study |
title | The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study |
title_full | The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study |
title_fullStr | The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study |
title_full_unstemmed | The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study |
title_short | The associations of DNA methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study |
title_sort | associations of dna methylation alterations in oxidative stress-related genes with cancer incidence and mortality outcomes: a population-based cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346508/ https://www.ncbi.nlm.nih.gov/pubmed/30678711 http://dx.doi.org/10.1186/s13148-018-0604-y |
work_keys_str_mv | AT gaoxin theassociationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT zhangyan theassociationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT burwinkelbarbara theassociationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT xuanyang theassociationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT holleczekbernd theassociationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT brennerhermann theassociationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT schottkerben theassociationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT gaoxin associationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT zhangyan associationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT burwinkelbarbara associationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT xuanyang associationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT holleczekbernd associationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT brennerhermann associationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy AT schottkerben associationsofdnamethylationalterationsinoxidativestressrelatedgeneswithcancerincidenceandmortalityoutcomesapopulationbasedcohortstudy |