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Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations

BACKGROUND: Lung cancer is the leading cause of cancer-related death. While cigarette smoking is the primary cause of this malignancy, risk differs across racial/ethnic groups. For the same number of cigarettes smoked, Native Hawaiians compared to whites are at greater risk and Japanese Americans ar...

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Autores principales: Park, Sungshim L., Patel, Yesha M., Loo, Lenora W. M., Mullen, Daniel J., Offringa, Ite A., Maunakea, Alika, Stram, Daniel O., Siegmund, Kimberly, Murphy, Sharon E., Tiirikainen, Maarit, Le Marchand, Loïc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108111/
https://www.ncbi.nlm.nih.gov/pubmed/30139389
http://dx.doi.org/10.1186/s13148-018-0543-7
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author Park, Sungshim L.
Patel, Yesha M.
Loo, Lenora W. M.
Mullen, Daniel J.
Offringa, Ite A.
Maunakea, Alika
Stram, Daniel O.
Siegmund, Kimberly
Murphy, Sharon E.
Tiirikainen, Maarit
Le Marchand, Loïc
author_facet Park, Sungshim L.
Patel, Yesha M.
Loo, Lenora W. M.
Mullen, Daniel J.
Offringa, Ite A.
Maunakea, Alika
Stram, Daniel O.
Siegmund, Kimberly
Murphy, Sharon E.
Tiirikainen, Maarit
Le Marchand, Loïc
author_sort Park, Sungshim L.
collection PubMed
description BACKGROUND: Lung cancer is the leading cause of cancer-related death. While cigarette smoking is the primary cause of this malignancy, risk differs across racial/ethnic groups. For the same number of cigarettes smoked, Native Hawaiians compared to whites are at greater risk and Japanese Americans are at lower risk of developing lung cancer. DNA methylation of specific CpG sites (e.g., in AHRR and F2RL3) is the most common blood epigenetic modification associated with smoking status. However, the influence of internal smoking dose, measured by urinary nicotine equivalents (NE), on DNA methylation in current smokers has not been investigated, nor has a study evaluated whether for the same smoking dose, circulating leukocyte DNA methylation patterns differ by race. METHODS: We conducted an epigenome-wide association study (EWAS) of NE in 612 smokers from three racial/ethnic groups: whites (n = 204), Native Hawaiians (n = 205), and Japanese Americans (n = 203). Genome-wide DNA methylation profiling of blood leukocyte DNA was measured using the Illumina 450K BeadChip array. Average β value, the ratio of signal from a methylated probe relative to the sum of the methylated and unmethylated probes at that CpG, was the dependent variables in linear regression models adjusting for age, sex, race (for pan-ethnic analysis), and estimated cell-type distribution. RESULTS: We found that NE was significantly associated with six differentially methylated CpG sites (Bonferroni corrected p < 1.48 × 10−7): four in or near the FOXK2, PBX1, FNDC7, and FUBP3 genes and two in non-annotated genetic regions. Higher levels of NE were associated with increasing methylation beta-valuesin all six sites. For all six CpG sites, the association was only observed in Native Hawaiians, suggesting that the influence of smoking dose on DNA methylation patterns is heterogeneous across race/ethnicity (p interactions < 8.8 × 10−8). We found two additional CpG sites associated with NE in only Native Hawaiians. CONCLUSIONS: In conclusion, internal smoking dose was associated with increased DNA methylation in circulating leukocytes at specific sites in Native Hawaiian smokers but not in white or Japanese American smokers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0543-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-61081112018-08-28 Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations Park, Sungshim L. Patel, Yesha M. Loo, Lenora W. M. Mullen, Daniel J. Offringa, Ite A. Maunakea, Alika Stram, Daniel O. Siegmund, Kimberly Murphy, Sharon E. Tiirikainen, Maarit Le Marchand, Loïc Clin Epigenetics Research BACKGROUND: Lung cancer is the leading cause of cancer-related death. While cigarette smoking is the primary cause of this malignancy, risk differs across racial/ethnic groups. For the same number of cigarettes smoked, Native Hawaiians compared to whites are at greater risk and Japanese Americans are at lower risk of developing lung cancer. DNA methylation of specific CpG sites (e.g., in AHRR and F2RL3) is the most common blood epigenetic modification associated with smoking status. However, the influence of internal smoking dose, measured by urinary nicotine equivalents (NE), on DNA methylation in current smokers has not been investigated, nor has a study evaluated whether for the same smoking dose, circulating leukocyte DNA methylation patterns differ by race. METHODS: We conducted an epigenome-wide association study (EWAS) of NE in 612 smokers from three racial/ethnic groups: whites (n = 204), Native Hawaiians (n = 205), and Japanese Americans (n = 203). Genome-wide DNA methylation profiling of blood leukocyte DNA was measured using the Illumina 450K BeadChip array. Average β value, the ratio of signal from a methylated probe relative to the sum of the methylated and unmethylated probes at that CpG, was the dependent variables in linear regression models adjusting for age, sex, race (for pan-ethnic analysis), and estimated cell-type distribution. RESULTS: We found that NE was significantly associated with six differentially methylated CpG sites (Bonferroni corrected p < 1.48 × 10−7): four in or near the FOXK2, PBX1, FNDC7, and FUBP3 genes and two in non-annotated genetic regions. Higher levels of NE were associated with increasing methylation beta-valuesin all six sites. For all six CpG sites, the association was only observed in Native Hawaiians, suggesting that the influence of smoking dose on DNA methylation patterns is heterogeneous across race/ethnicity (p interactions < 8.8 × 10−8). We found two additional CpG sites associated with NE in only Native Hawaiians. CONCLUSIONS: In conclusion, internal smoking dose was associated with increased DNA methylation in circulating leukocytes at specific sites in Native Hawaiian smokers but not in white or Japanese American smokers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13148-018-0543-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-23 /pmc/articles/PMC6108111/ /pubmed/30139389 http://dx.doi.org/10.1186/s13148-018-0543-7 Text en © The Author(s). 2018 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
Park, Sungshim L.
Patel, Yesha M.
Loo, Lenora W. M.
Mullen, Daniel J.
Offringa, Ite A.
Maunakea, Alika
Stram, Daniel O.
Siegmund, Kimberly
Murphy, Sharon E.
Tiirikainen, Maarit
Le Marchand, Loïc
Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations
title Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations
title_full Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations
title_fullStr Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations
title_full_unstemmed Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations
title_short Association of internal smoking dose with blood DNA methylation in three racial/ethnic populations
title_sort association of internal smoking dose with blood dna methylation in three racial/ethnic populations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108111/
https://www.ncbi.nlm.nih.gov/pubmed/30139389
http://dx.doi.org/10.1186/s13148-018-0543-7
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