Abstract

BackgroundHigh serum levels of estradiol are associated with increased risk of postmenopausal breast cancer. Little is known about the gene expression in normal breast tissue in relation to levels of circulating serum estradiol.MethodsWe compared whole genome expression data of breast tissue samples with serum hormone levels using data from 79 healthy women and 64 breast cancer patients. Significance analysis of microarrays (SAM) was used to identify differentially expressed genes and multivariate linear regression was used to identify independent associations.ResultsSix genes (SCGB3A1, RSPO1, TLN2, SLITRK4, DCLK1, PTGS1) were found differentially expressed according to serum estradiol levels (FDR = 0). Three of these independently predicted estradiol levels in a multivariate model, as SCGB3A1 (HIN1) and TLN2 were up-regulated and PTGS1 (COX1) was down-regulated in breast samples from women with high serum estradiol. Serum estradiol, but none of the differentially expressed genes were significantly associated with mammographic density, another strong breast cancer risk factor. In breast carcinomas, expression of GREB1 and AREG was associated with serum estradiol in all cancers and in the subgroup of estrogen receptor positive cases.ConclusionsWe have identified genes associated with serum estradiol levels in normal breast tissue and in breast carcinomas. SCGB3A1 is a suggested tumor suppressor gene that inhibits cell growth and invasion and is methylated and down-regulated in many epithelial cancers. Our findings indicate this gene as an important inhibitor of breast cell proliferation in healthy women with high estradiol levels. In the breast, this gene is expressed in luminal cells only and is methylated in non-BRCA-related breast cancers. The possibility of a carcinogenic contribution of silencing of this gene for luminal, but not basal-like cancers should be further explored. PTGS1 induces prostaglandin E2 (PGE2) production which in turn stimulates aromatase expression and hence increases the local production of estradiol. This is the first report studying such associations in normal breast tissue in humans.

Highlights

  • High serum levels of estradiol are associated with increased risk of postmenopausal breast cancer

  • There were no significant gene ontology terms enriched in the down-regulated genes with FDR < 50 (n = 8), response to steroid hormone stimulus was the most enriched term with three observed genes (prostaglandin-endoperoxide synthase 1 (PTGS1), ESR1 and GATA3)(Additional file 2)

  • The expression in breast carcinomas was similar to that in normal tissue from women with lower levels of circulating estradiol and opposite to that found in normal samples from women with higher levels of serum estradiol (Table 1)

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Summary

Introduction

High serum levels of estradiol are associated with increased risk of postmenopausal breast cancer. In estrogen receptor (ER) positive breast carcinomas, the proliferating tumor cells express ER while in normal breast tissue the proliferating epithelial cells are ER negative (ER-) [8,9]. Both normal and malignant breast epithelial cells are influenced by estradiol but through different mechanisms. A study reported an association between serum levels of estradiol and gene expression of trefoil factor 1 (TFF1), growth regulation by estrogen in breast cancer 1 (GREB1), PDZ domain containing 1 (PDZK1) and progesterone receptor (PGR) in ER+ breast carcinomas [10]. This strengthens the hypothesis that serum estradiol levels influence the gene expression in breast tissue

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