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Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55

BACKGROUND: Mammographic density (MD) has been found to be an independent risk factor for breast cancer. Although data from twin studies suggest that MD has a strong genetic component, the exact genes involved remain to be identified. Alterations in stromal composition and the number of epithelial c...

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Autores principales: Ozhand, Ali, Lee, Eunjung, Wu, Anna H., Ellingjord-Dale, Merete, Akslen, Lars A., McKean-Cowdin, Roberta, Ursin, Giske
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3676419/
https://www.ncbi.nlm.nih.gov/pubmed/23762340
http://dx.doi.org/10.1371/journal.pone.0065313
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author Ozhand, Ali
Lee, Eunjung
Wu, Anna H.
Ellingjord-Dale, Merete
Akslen, Lars A.
McKean-Cowdin, Roberta
Ursin, Giske
author_facet Ozhand, Ali
Lee, Eunjung
Wu, Anna H.
Ellingjord-Dale, Merete
Akslen, Lars A.
McKean-Cowdin, Roberta
Ursin, Giske
author_sort Ozhand, Ali
collection PubMed
description BACKGROUND: Mammographic density (MD) has been found to be an independent risk factor for breast cancer. Although data from twin studies suggest that MD has a strong genetic component, the exact genes involved remain to be identified. Alterations in stromal composition and the number of epithelial cells are the most predominant histopathological determinants of mammographic density. Interactions between the breast stroma and epithelium are critically important in the maturation and development of the mammary gland and the cross-talk between these cells are mediated by paracrine growth factors and cytokines. The potential impact of genetic variation in growth factors and cytokines on MD is largely unknown. METHODS: We investigated the association between 89 single nucleotide polymorphisms (SNPs) in 7 cytokine/growth-factor genes (FGFR2, IGFBP1, IGFBP3, TGFB1, TNF, VEGF, IL6) and percent MD in 301 premenopausal women (aged 50 to 55 years) participating in the Norwegian Breast Cancer Screening Program. We evaluated the suggestive associations in 216 premenopausal Singapore Chinese Women of the same age. RESULTS: We found statistically significant associations between 9 tagging SNPs in the IL6 gene and MD in Norwegian women; the effect ranged from 3–5% in MD per variant allele (p-values = 0.02 to 0.0002). One SNP in the IL6 (rs10242595) significantly influenced MD in Singapore Chinese women. CONCLUSION: Genetic variations in IL6 may be associated with MD and therefore may be an indicator of breast cancer risk in premenopausal women.
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spelling pubmed-36764192013-06-12 Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55 Ozhand, Ali Lee, Eunjung Wu, Anna H. Ellingjord-Dale, Merete Akslen, Lars A. McKean-Cowdin, Roberta Ursin, Giske PLoS One Research Article BACKGROUND: Mammographic density (MD) has been found to be an independent risk factor for breast cancer. Although data from twin studies suggest that MD has a strong genetic component, the exact genes involved remain to be identified. Alterations in stromal composition and the number of epithelial cells are the most predominant histopathological determinants of mammographic density. Interactions between the breast stroma and epithelium are critically important in the maturation and development of the mammary gland and the cross-talk between these cells are mediated by paracrine growth factors and cytokines. The potential impact of genetic variation in growth factors and cytokines on MD is largely unknown. METHODS: We investigated the association between 89 single nucleotide polymorphisms (SNPs) in 7 cytokine/growth-factor genes (FGFR2, IGFBP1, IGFBP3, TGFB1, TNF, VEGF, IL6) and percent MD in 301 premenopausal women (aged 50 to 55 years) participating in the Norwegian Breast Cancer Screening Program. We evaluated the suggestive associations in 216 premenopausal Singapore Chinese Women of the same age. RESULTS: We found statistically significant associations between 9 tagging SNPs in the IL6 gene and MD in Norwegian women; the effect ranged from 3–5% in MD per variant allele (p-values = 0.02 to 0.0002). One SNP in the IL6 (rs10242595) significantly influenced MD in Singapore Chinese women. CONCLUSION: Genetic variations in IL6 may be associated with MD and therefore may be an indicator of breast cancer risk in premenopausal women. Public Library of Science 2013-06-07 /pmc/articles/PMC3676419/ /pubmed/23762340 http://dx.doi.org/10.1371/journal.pone.0065313 Text en © 2013 Ozhand 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ozhand, Ali
Lee, Eunjung
Wu, Anna H.
Ellingjord-Dale, Merete
Akslen, Lars A.
McKean-Cowdin, Roberta
Ursin, Giske
Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55
title Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55
title_full Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55
title_fullStr Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55
title_full_unstemmed Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55
title_short Variation in Inflammatory Cytokine/Growth-Factor Genes and Mammographic Density in Premenopausal Women Aged 50–55
title_sort variation in inflammatory cytokine/growth-factor genes and mammographic density in premenopausal women aged 50–55
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3676419/
https://www.ncbi.nlm.nih.gov/pubmed/23762340
http://dx.doi.org/10.1371/journal.pone.0065313
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