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DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women
Several studies have found aberrant DNA methylation levels in breast cancer cases, but factors influencing DNA methylation patterns and the mechanisms are not well understood. This case–control study evaluated blood methylation level of two repetitive elements and selected breast cancer‐related gene...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540549/ https://www.ncbi.nlm.nih.gov/pubmed/32352194 http://dx.doi.org/10.1111/bcpt.13424 |
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author | Wielsøe, Maria Tarantini, Letizia Bollati, Valentina Long, Manhai Bonefeld‐Jørgensen, Eva Cecilie |
author_facet | Wielsøe, Maria Tarantini, Letizia Bollati, Valentina Long, Manhai Bonefeld‐Jørgensen, Eva Cecilie |
author_sort | Wielsøe, Maria |
collection | PubMed |
description | Several studies have found aberrant DNA methylation levels in breast cancer cases, but factors influencing DNA methylation patterns and the mechanisms are not well understood. This case–control study evaluated blood methylation level of two repetitive elements and selected breast cancer‐related genes in relation to breast cancer risk, and the associations with serum level of persistent organic pollutants (POPs) and breast cancer risk factors in Greenlandic Inuit. DNA methylation was determined using bisulphite pyrosequencing in blood from 74 breast cancer cases and 80 controls. Using first tertile as reference, the following was observed. Positive associations for ATM in second tertile (OR: 2.33, 95% CI: 1.04; 5.23) and ESR2 in third tertile (OR: 2.22, 95% CI: 0.97; 5.05) suggest an increased breast cancer risk with high DNA methylation. LINE‐1 methylation was lower in cases than controls. In third tertile (OR: 0.42, 95% CI: 0.18; 0.98), associations suggest in accordance with the literature an increased risk of breast cancer with LINE‐1 hypomethylation. Among controls, significant associations between methylation levels and serum level of POPs and breast cancer risk factors (age, body mass index, cotinine level) were found. Thus, breast cancer risk factors and POPs may alter the risk through changes in methylation levels; further studies are needed to elucidate the mechanisms. |
format | Online Article Text |
id | pubmed-7540549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75405492020-10-09 DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women Wielsøe, Maria Tarantini, Letizia Bollati, Valentina Long, Manhai Bonefeld‐Jørgensen, Eva Cecilie Basic Clin Pharmacol Toxicol ORIGINAL ARTICLES Several studies have found aberrant DNA methylation levels in breast cancer cases, but factors influencing DNA methylation patterns and the mechanisms are not well understood. This case–control study evaluated blood methylation level of two repetitive elements and selected breast cancer‐related genes in relation to breast cancer risk, and the associations with serum level of persistent organic pollutants (POPs) and breast cancer risk factors in Greenlandic Inuit. DNA methylation was determined using bisulphite pyrosequencing in blood from 74 breast cancer cases and 80 controls. Using first tertile as reference, the following was observed. Positive associations for ATM in second tertile (OR: 2.33, 95% CI: 1.04; 5.23) and ESR2 in third tertile (OR: 2.22, 95% CI: 0.97; 5.05) suggest an increased breast cancer risk with high DNA methylation. LINE‐1 methylation was lower in cases than controls. In third tertile (OR: 0.42, 95% CI: 0.18; 0.98), associations suggest in accordance with the literature an increased risk of breast cancer with LINE‐1 hypomethylation. Among controls, significant associations between methylation levels and serum level of POPs and breast cancer risk factors (age, body mass index, cotinine level) were found. Thus, breast cancer risk factors and POPs may alter the risk through changes in methylation levels; further studies are needed to elucidate the mechanisms. John Wiley and Sons Inc. 2020-05-18 2020-10 /pmc/articles/PMC7540549/ /pubmed/32352194 http://dx.doi.org/10.1111/bcpt.13424 Text en © 2020 The Authors. Basic & Clinical Pharmacology & Toxicology published by John Wiley & Sons Ltd on behalf of Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society) This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | ORIGINAL ARTICLES Wielsøe, Maria Tarantini, Letizia Bollati, Valentina Long, Manhai Bonefeld‐Jørgensen, Eva Cecilie DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women |
title | DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women |
title_full | DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women |
title_fullStr | DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women |
title_full_unstemmed | DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women |
title_short | DNA methylation level in blood and relations to breast cancer, risk factors and environmental exposure in Greenlandic Inuit women |
title_sort | dna methylation level in blood and relations to breast cancer, risk factors and environmental exposure in greenlandic inuit women |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540549/ https://www.ncbi.nlm.nih.gov/pubmed/32352194 http://dx.doi.org/10.1111/bcpt.13424 |
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