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Alcohol consumption and breast tumor gene expression

BACKGROUND: Alcohol consumption is an established risk factor for breast cancer and the association generally appears stronger among estrogen receptor (ER)-positive tumors. However, the biological mechanisms underlying this association are not completely understood. METHODS: We analyzed messenger RN...

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Autores principales: Wang, Jun, Heng, Yujing J., Eliassen, A. Heather, Tamimi, Rulla M., Hazra, Aditi, Carey, Vincent J., Ambrosone, Christine B., de Andrade, Victor P., Brufsky, Adam, Couch, Fergus J., King, Tari A., Modugno, Francesmary, Vachon, Celine M., Hunter, David J., Beck, Andrew H., Hankinson, Susan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596493/
https://www.ncbi.nlm.nih.gov/pubmed/28899409
http://dx.doi.org/10.1186/s13058-017-0901-y
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author Wang, Jun
Heng, Yujing J.
Eliassen, A. Heather
Tamimi, Rulla M.
Hazra, Aditi
Carey, Vincent J.
Ambrosone, Christine B.
de Andrade, Victor P.
Brufsky, Adam
Couch, Fergus J.
King, Tari A.
Modugno, Francesmary
Vachon, Celine M.
Hunter, David J.
Beck, Andrew H.
Hankinson, Susan E.
author_facet Wang, Jun
Heng, Yujing J.
Eliassen, A. Heather
Tamimi, Rulla M.
Hazra, Aditi
Carey, Vincent J.
Ambrosone, Christine B.
de Andrade, Victor P.
Brufsky, Adam
Couch, Fergus J.
King, Tari A.
Modugno, Francesmary
Vachon, Celine M.
Hunter, David J.
Beck, Andrew H.
Hankinson, Susan E.
author_sort Wang, Jun
collection PubMed
description BACKGROUND: Alcohol consumption is an established risk factor for breast cancer and the association generally appears stronger among estrogen receptor (ER)-positive tumors. However, the biological mechanisms underlying this association are not completely understood. METHODS: We analyzed messenger RNA (mRNA) microarray data from both invasive breast tumors (N = 602) and tumor-adjacent normal tissues (N = 508) from participants diagnosed with breast cancer in the Nurses’ Health Study (NHS) and NHSII. Multivariable linear regression, controlling for other known breast cancer risk factors, was used to identify differentially expressed genes by pre-diagnostic alcohol intake. For pathway analysis, we performed gene set enrichment analysis (GSEA). Differentially expressed genes or enriched pathway-defined gene sets with false discovery rate (FDR) <0.1 identified in tumors were validated in RNA sequencing data of invasive breast tumors (N = 166) from The Cancer Genome Atlas. RESULTS: No individual genes were significantly differentially expressed by alcohol consumption in the NHS/NHSII. However, GSEA identified 33 and 68 pathway-defined gene sets at FDR <0.1 among 471 ER+ and 127 ER- tumors, respectively, all of which were validated. Among ER+ tumors, consuming 10+ grams of alcohol per day (vs. 0) was associated with upregulation in RNA metabolism and transport, cell cycle regulation, and DNA repair, and downregulation in lipid metabolism. Among ER- tumors, in addition to upregulation in RNA processing and cell cycle, alcohol intake was linked to overexpression of genes involved in cytokine signaling, including interferon and transforming growth factor (TGF)-β signaling pathways, and translation and post-translational modifications. Lower lipid metabolism was observed in both ER+ tumors and ER+ tumor-adjacent normal samples. Most of the significantly enriched gene sets identified in ER- tumors showed a similar enrichment pattern among ER- tumor-adjacent normal tissues. CONCLUSIONS: Our data suggest that moderate alcohol consumption (i.e. 10+ grams/day, equivalent to one or more drinks/day) is associated with several specific and reproducible biological processes and pathways, which adds potential new insight into alcohol-related breast carcinogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-017-0901-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-55964932017-09-15 Alcohol consumption and breast tumor gene expression Wang, Jun Heng, Yujing J. Eliassen, A. Heather Tamimi, Rulla M. Hazra, Aditi Carey, Vincent J. Ambrosone, Christine B. de Andrade, Victor P. Brufsky, Adam Couch, Fergus J. King, Tari A. Modugno, Francesmary Vachon, Celine M. Hunter, David J. Beck, Andrew H. Hankinson, Susan E. Breast Cancer Res Research Article BACKGROUND: Alcohol consumption is an established risk factor for breast cancer and the association generally appears stronger among estrogen receptor (ER)-positive tumors. However, the biological mechanisms underlying this association are not completely understood. METHODS: We analyzed messenger RNA (mRNA) microarray data from both invasive breast tumors (N = 602) and tumor-adjacent normal tissues (N = 508) from participants diagnosed with breast cancer in the Nurses’ Health Study (NHS) and NHSII. Multivariable linear regression, controlling for other known breast cancer risk factors, was used to identify differentially expressed genes by pre-diagnostic alcohol intake. For pathway analysis, we performed gene set enrichment analysis (GSEA). Differentially expressed genes or enriched pathway-defined gene sets with false discovery rate (FDR) <0.1 identified in tumors were validated in RNA sequencing data of invasive breast tumors (N = 166) from The Cancer Genome Atlas. RESULTS: No individual genes were significantly differentially expressed by alcohol consumption in the NHS/NHSII. However, GSEA identified 33 and 68 pathway-defined gene sets at FDR <0.1 among 471 ER+ and 127 ER- tumors, respectively, all of which were validated. Among ER+ tumors, consuming 10+ grams of alcohol per day (vs. 0) was associated with upregulation in RNA metabolism and transport, cell cycle regulation, and DNA repair, and downregulation in lipid metabolism. Among ER- tumors, in addition to upregulation in RNA processing and cell cycle, alcohol intake was linked to overexpression of genes involved in cytokine signaling, including interferon and transforming growth factor (TGF)-β signaling pathways, and translation and post-translational modifications. Lower lipid metabolism was observed in both ER+ tumors and ER+ tumor-adjacent normal samples. Most of the significantly enriched gene sets identified in ER- tumors showed a similar enrichment pattern among ER- tumor-adjacent normal tissues. CONCLUSIONS: Our data suggest that moderate alcohol consumption (i.e. 10+ grams/day, equivalent to one or more drinks/day) is associated with several specific and reproducible biological processes and pathways, which adds potential new insight into alcohol-related breast carcinogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-017-0901-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-12 2017 /pmc/articles/PMC5596493/ /pubmed/28899409 http://dx.doi.org/10.1186/s13058-017-0901-y Text en © The Author(s). 2017 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 Article
Wang, Jun
Heng, Yujing J.
Eliassen, A. Heather
Tamimi, Rulla M.
Hazra, Aditi
Carey, Vincent J.
Ambrosone, Christine B.
de Andrade, Victor P.
Brufsky, Adam
Couch, Fergus J.
King, Tari A.
Modugno, Francesmary
Vachon, Celine M.
Hunter, David J.
Beck, Andrew H.
Hankinson, Susan E.
Alcohol consumption and breast tumor gene expression
title Alcohol consumption and breast tumor gene expression
title_full Alcohol consumption and breast tumor gene expression
title_fullStr Alcohol consumption and breast tumor gene expression
title_full_unstemmed Alcohol consumption and breast tumor gene expression
title_short Alcohol consumption and breast tumor gene expression
title_sort alcohol consumption and breast tumor gene expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596493/
https://www.ncbi.nlm.nih.gov/pubmed/28899409
http://dx.doi.org/10.1186/s13058-017-0901-y
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