Candidate Gene DNA Methylation Associations with Breast Cancer Characteristics and Tumor Progression
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2018/04/01
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Description:Aim: We examined methylation patterns with aggressive tumor phenotypes and investigated demographic, socioeconomic and reproductive predictors of gene methylation. Materials & methods: Pyrosequencing quantified methylation of BRCA1, EGFR, GSTM2, RASSF1, TFF1 and Sat 2. We used quantile regression models to calculate adjusted median methylation values by estrogen and progesterone receptor (ER/PR) status. Bivariate associations between participant characteristics and methylation were examined. Results: Higher percent methylation of GSTM2 was observed in ER/PR-negative compared with ER/PR-positive tumors in ductal carcinoma in situ (14 vs 2%) and invasive (35 vs 3%) tissue components. Trends in aberrant GSTM2 methylation across tissue components were stronger among ER/PR-negative tumors (p-interaction <0.001). Black women were more likely to have ER/PR-negative tumors (p = 0.01) and show hypermethylation of GSTM2 compared with other women (p = 0.05). Conclusion: GSTM2 promoter hypermethylation may serve as a potential biomarker of aggressive tumor development and a mechanism for ER/PR-negative tumor progression. [Description provided by NIOSH]
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ISSN:1750-1911
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Pages in Document:367-378
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Volume:10
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Issue:4
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NIOSHTIC Number:nn:20063616
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Citation:Epigenomics 2018 Apr; 10(4):367-378
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Contact Point Address:Jacob K Kresovich, Division of Epidemiology & Biostatistics, University of Illinois at Chicago School of Public Health, Chicago, IL 60612, USA
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Email:jacob.kresovich@nih.gov
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Federal Fiscal Year:2018
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Performing Organization:University of Illinois at Chicago
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Peer Reviewed:True
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Start Date:20050701
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Source Full Name:Epigenomics
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End Date:20290630
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Main Document Checksum:urn:sha-512:75a043c66980ba74c82950dedd44594da56eaa6d85f2f8fe87596c88861ccd32781783e888527d516a62a5a69a457e705fba99a8bf1b3f1272b9b04672306f28
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