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National Institute of Environmental Health Sciences

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Publication Detail

Title: Hormone therapy use and breast tissue DNA methylation: analysis of epigenome wide data from the normal breast study.

Authors: Harlid, Sophia; Xu, Zongli; Kirk, Erin; Wilson, Lauren E; Troester, Melissa A; Taylor, Jack A

Published In Epigenetics, (2019 02)

Abstract: Hormone therapy (HT) is associated with increased risk of breast cancer, strongly dependent on type, duration, and recency of use. HT use could affect cancer risk by changing breast tissue transcriptional programs. We hypothesize that these changes are preceded by changes in DNA methylation. To explore this hypothesis we used histologically normal-appearing breast tissue from the Normal Breast Study (NBS). DNA methylation β-values were obtained using the Illumina HumanMethylation 450 BeadChips for 90 samples including all NBS-participants who used HT within 5 y before surgery. Data were analyzed using the reference-free cell mixture method. Cancer Genome Atlas (TCGA) mRNA-Seq data were used to assess correlation between DNA methylation and gene expression. We identified 527 CpG sites in 403 genes that were associated with ever using HT at genome wide significance (FDR q < 0.05), of these, 68 sites were also significantly associated with duration of use or recency of use. Twelve sites reached significance in all analyses one of which was cg01382688 in ARHGEF4 (p < 1.2x10-7). Mutations in ARHGEF4 have been reported in breast tumors, but this is the first report of possible breast cancer-related DNA methylation changes. In addition, 22 genes included more than one significant CpG site and a majority of these sites were significantly correlated with gene expression. Although based on small numbers, these findings support the hypothesis that HT is associated with epigenetic alterations in breast tissue, and identifies genes with altered DNA methylation states which could be linked to breast cancer development.

PubMed ID: 30821641 Exiting the NIEHS site

MeSH Terms: Adult; Aged; Aged, 80 and over; Breast Neoplasms/chemically induced; Breast Neoplasms/genetics*; CpG Islands; DNA Methylation*/drug effects; Epigenesis, Genetic; Estrogens/adverse effects*; Female; Gene Expression Profiling/methods*; Gene Expression Regulation, Neoplastic; Genome-Wide Association Study/methods; High-Throughput Nucleotide Sequencing; Humans; Middle Aged; Progesterone/adverse effects*; Sequence Analysis, DNA; Sequence Analysis, RNA

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