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PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants

BACKGROUND: Particulate matter (PM) < 2.5 μm (PM(2.5)) or fine PM is a serious public health concern. It affects DNA methylation and heightens carcinogenesis. Deleted in lung and esophageal cancer 1 (DLEC1) is a tumor suppressor gene. However, aberrant methylation of the gene is associated with s...

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Autores principales: Chou, Ying-Hsiang, Tantoh, Disline Manli, Wu, Ming-Chi, Tyan, Yeu-Sheng, Chen, Pei-Hsin, Nfor, Oswald Ndi, Hsu, Shu-Yi, Shen, Chao-Yu, Huang, Chien-Ning, Liaw, Yung-Po
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646067/
https://www.ncbi.nlm.nih.gov/pubmed/33153431
http://dx.doi.org/10.1186/s12199-020-00909-x
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author Chou, Ying-Hsiang
Tantoh, Disline Manli
Wu, Ming-Chi
Tyan, Yeu-Sheng
Chen, Pei-Hsin
Nfor, Oswald Ndi
Hsu, Shu-Yi
Shen, Chao-Yu
Huang, Chien-Ning
Liaw, Yung-Po
author_facet Chou, Ying-Hsiang
Tantoh, Disline Manli
Wu, Ming-Chi
Tyan, Yeu-Sheng
Chen, Pei-Hsin
Nfor, Oswald Ndi
Hsu, Shu-Yi
Shen, Chao-Yu
Huang, Chien-Ning
Liaw, Yung-Po
author_sort Chou, Ying-Hsiang
collection PubMed
description BACKGROUND: Particulate matter (PM) < 2.5 μm (PM(2.5)) or fine PM is a serious public health concern. It affects DNA methylation and heightens carcinogenesis. Deleted in lung and esophageal cancer 1 (DLEC1) is a tumor suppressor gene. However, aberrant methylation of the gene is associated with several cancers. We evaluated the association between PM(2.5) and DLEC1 promoter methylation in Taiwanese adults based on regular outdoor exercise. METHODS: We obtained DNA methylation and exercise data of 496 participants (aged between 30 and 70 years) from the Taiwan Biobank (TWB) database. We also extracted PM(2.5) data from the Air Quality Monitoring Database (AQMD) and estimated participants’ exposure using residential addresses. RESULTS: DLEC1 methylation and PM(2.5) were positively associated: beta coefficient (β) = 0.114 × 10(−3); p value = 0.046. The test for interaction between exercise and PM(2.5) on DLEC1 methylation was significant (p value = 0.036). After stratification by exercise habits, PM(2.5) and DLEC1 methylation remained significantly associated only among those who exercised regularly (β = 0.237 × 10(−3); p value = 0.007). PM(2.5) quartile-stratified analyses revealed an inverse association between regular exercise and DLEC1 methylation at PM(2.5) < 27.37 μg/m(3) (β = − 5.280 × 10(−3); p value = 0.009). After combining exercise habits and PM(2.5) quartiles, one stratum (i.e., regular exercise and PM(2.5) < 27.37 μg/m(3)) was inversely associated with DLEC1 methylation (β = -5.160 × 10(−3), p value = 0.007). CONCLUSIONS: We found significant positive associations between PM(2.5) and DLEC1 promoter methylation. Regular exercise at PM(2.5) < 27.37 μg/m(3) seemingly regulated DLEC1 promoter methylation.
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spelling pubmed-76460672020-11-06 PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants Chou, Ying-Hsiang Tantoh, Disline Manli Wu, Ming-Chi Tyan, Yeu-Sheng Chen, Pei-Hsin Nfor, Oswald Ndi Hsu, Shu-Yi Shen, Chao-Yu Huang, Chien-Ning Liaw, Yung-Po Environ Health Prev Med Research Article BACKGROUND: Particulate matter (PM) < 2.5 μm (PM(2.5)) or fine PM is a serious public health concern. It affects DNA methylation and heightens carcinogenesis. Deleted in lung and esophageal cancer 1 (DLEC1) is a tumor suppressor gene. However, aberrant methylation of the gene is associated with several cancers. We evaluated the association between PM(2.5) and DLEC1 promoter methylation in Taiwanese adults based on regular outdoor exercise. METHODS: We obtained DNA methylation and exercise data of 496 participants (aged between 30 and 70 years) from the Taiwan Biobank (TWB) database. We also extracted PM(2.5) data from the Air Quality Monitoring Database (AQMD) and estimated participants’ exposure using residential addresses. RESULTS: DLEC1 methylation and PM(2.5) were positively associated: beta coefficient (β) = 0.114 × 10(−3); p value = 0.046. The test for interaction between exercise and PM(2.5) on DLEC1 methylation was significant (p value = 0.036). After stratification by exercise habits, PM(2.5) and DLEC1 methylation remained significantly associated only among those who exercised regularly (β = 0.237 × 10(−3); p value = 0.007). PM(2.5) quartile-stratified analyses revealed an inverse association between regular exercise and DLEC1 methylation at PM(2.5) < 27.37 μg/m(3) (β = − 5.280 × 10(−3); p value = 0.009). After combining exercise habits and PM(2.5) quartiles, one stratum (i.e., regular exercise and PM(2.5) < 27.37 μg/m(3)) was inversely associated with DLEC1 methylation (β = -5.160 × 10(−3), p value = 0.007). CONCLUSIONS: We found significant positive associations between PM(2.5) and DLEC1 promoter methylation. Regular exercise at PM(2.5) < 27.37 μg/m(3) seemingly regulated DLEC1 promoter methylation. BioMed Central 2020-11-05 2020 /pmc/articles/PMC7646067/ /pubmed/33153431 http://dx.doi.org/10.1186/s12199-020-00909-x Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Chou, Ying-Hsiang
Tantoh, Disline Manli
Wu, Ming-Chi
Tyan, Yeu-Sheng
Chen, Pei-Hsin
Nfor, Oswald Ndi
Hsu, Shu-Yi
Shen, Chao-Yu
Huang, Chien-Ning
Liaw, Yung-Po
PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants
title PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants
title_full PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants
title_fullStr PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants
title_full_unstemmed PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants
title_short PM(2.5) exposure and DLEC1 promoter methylation in Taiwan Biobank participants
title_sort pm(2.5) exposure and dlec1 promoter methylation in taiwan biobank participants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646067/
https://www.ncbi.nlm.nih.gov/pubmed/33153431
http://dx.doi.org/10.1186/s12199-020-00909-x
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