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Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk

BACKGROUND: Inflammation contributes to breast cancer development through its effects on cell damage. This damage is usually dealt with by key genes involved in apoptosis and autophagy pathways. METHODS: We tested 206 single nucleotide polymorphisms (SNPs) in 54 genes related to inflammation, apopto...

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Autores principales: Schuetz, Johanna M., Grundy, Anne, Lee, Derrick G., Lai, Agnes S., Kobayashi, Lindsay C., Richardson, Harriet, Long, Jirong, Zheng, Wei, Aronson, Kristan J., Spinelli, John J., Brooks-Wilson, Angela R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314637/
https://www.ncbi.nlm.nih.gov/pubmed/30601841
http://dx.doi.org/10.1371/journal.pone.0209010
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author Schuetz, Johanna M.
Grundy, Anne
Lee, Derrick G.
Lai, Agnes S.
Kobayashi, Lindsay C.
Richardson, Harriet
Long, Jirong
Zheng, Wei
Aronson, Kristan J.
Spinelli, John J.
Brooks-Wilson, Angela R.
author_facet Schuetz, Johanna M.
Grundy, Anne
Lee, Derrick G.
Lai, Agnes S.
Kobayashi, Lindsay C.
Richardson, Harriet
Long, Jirong
Zheng, Wei
Aronson, Kristan J.
Spinelli, John J.
Brooks-Wilson, Angela R.
author_sort Schuetz, Johanna M.
collection PubMed
description BACKGROUND: Inflammation contributes to breast cancer development through its effects on cell damage. This damage is usually dealt with by key genes involved in apoptosis and autophagy pathways. METHODS: We tested 206 single nucleotide polymorphisms (SNPs) in 54 genes related to inflammation, apoptosis and autophagy in a population-based breast cancer study of women of European (658 cases and 795 controls) and East Asian (262 cases and 127 controls) descent. Logistic regression was used to estimate odds ratios for breast cancer risk, and case-only analysis to compare breast cancer subtypes (defined by ER/PR/HER2 status), with adjustment for confounders. We assessed statistical interactions between the SNPs and lifestyle factors (smoking status, physical activity and body mass index). RESULTS AND CONCLUSION: Although no SNP was associated with breast cancer risk among women of European descent, we found evidence for an association among East Asians for rs1800925 (IL-13) and breast cancer risk (OR = 2.08; 95% CI: 1.32–3.28; p = 0.000779), which remained statistically significant after multiple testing correction (p(adj) = 0.0350). This association was replicated in a meta-analysis of 4305 cases and 4194 controls in the Shanghai Breast Cancer Genetics Study (OR 1.12, 95% CI: 1.03–1.21, p = 0.011). Further, we found evidence of an interaction between rs7874234 (TSC1) and physical activity among women of East Asian descent.
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spelling pubmed-63146372019-01-11 Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk Schuetz, Johanna M. Grundy, Anne Lee, Derrick G. Lai, Agnes S. Kobayashi, Lindsay C. Richardson, Harriet Long, Jirong Zheng, Wei Aronson, Kristan J. Spinelli, John J. Brooks-Wilson, Angela R. PLoS One Research Article BACKGROUND: Inflammation contributes to breast cancer development through its effects on cell damage. This damage is usually dealt with by key genes involved in apoptosis and autophagy pathways. METHODS: We tested 206 single nucleotide polymorphisms (SNPs) in 54 genes related to inflammation, apoptosis and autophagy in a population-based breast cancer study of women of European (658 cases and 795 controls) and East Asian (262 cases and 127 controls) descent. Logistic regression was used to estimate odds ratios for breast cancer risk, and case-only analysis to compare breast cancer subtypes (defined by ER/PR/HER2 status), with adjustment for confounders. We assessed statistical interactions between the SNPs and lifestyle factors (smoking status, physical activity and body mass index). RESULTS AND CONCLUSION: Although no SNP was associated with breast cancer risk among women of European descent, we found evidence for an association among East Asians for rs1800925 (IL-13) and breast cancer risk (OR = 2.08; 95% CI: 1.32–3.28; p = 0.000779), which remained statistically significant after multiple testing correction (p(adj) = 0.0350). This association was replicated in a meta-analysis of 4305 cases and 4194 controls in the Shanghai Breast Cancer Genetics Study (OR 1.12, 95% CI: 1.03–1.21, p = 0.011). Further, we found evidence of an interaction between rs7874234 (TSC1) and physical activity among women of East Asian descent. Public Library of Science 2019-01-02 /pmc/articles/PMC6314637/ /pubmed/30601841 http://dx.doi.org/10.1371/journal.pone.0209010 Text en © 2019 Schuetz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Schuetz, Johanna M.
Grundy, Anne
Lee, Derrick G.
Lai, Agnes S.
Kobayashi, Lindsay C.
Richardson, Harriet
Long, Jirong
Zheng, Wei
Aronson, Kristan J.
Spinelli, John J.
Brooks-Wilson, Angela R.
Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk
title Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk
title_full Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk
title_fullStr Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk
title_full_unstemmed Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk
title_short Genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk
title_sort genetic variants in genes related to inflammation, apoptosis and autophagy in breast cancer risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314637/
https://www.ncbi.nlm.nih.gov/pubmed/30601841
http://dx.doi.org/10.1371/journal.pone.0209010
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