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Epigenetic Changes of the Esr1 Gene in Breast Tissue of Healthy Women: A Missing Link With Breast Cancer Risk Factors? Publisher Pubmed



Daraei A1 ; Izadi P1 ; Khorasani G2 ; Nafissi N3 ; Naghizadeh MM4 ; Younosi N5 ; Meysamie A6 ; Mansoori Y4 ; Bastami M7 ; Tavakkolybazzaz J1
Authors
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Authors Affiliations
  1. 1. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, 14176-13151, Iran
  2. 2. Division of Plastic and Reconstructive Surgery, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Surgical Department, School of Medicine, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran
  5. 5. Surgical Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  6. 6. Community and Preventive Medicine Department, Medical Faculty, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran

Source: Genetic Testing and Molecular Biomarkers Published:2017


Abstract

Background: Reproductive history and obesity are among the well-recognized risk factors in the development of breast cancer, which are partially mediated by the increased exposure of breast tissues to estrogens. However, only a few studies have investigated the link between these risk factors and the pattern of methylation signatures in the breast tissue of healthy women. The role of the estrogen receptor 1 (ESR1) gene hypermethylation is reportedly important in the development of breast cancer. Thus, it is speculated that such ESR1 epigenetic changes may be influenced or shaped by obesity and reproductive history-related factors before and during breast carcinogenesis. Materials and Methods: Breast samples were collected from 120 cancer-free women who had undergone cosmetic mammoplasty. DNA was extracted from the breast tissues and, then, the methylation levels at the promoter and exon 1 regions of the ESR1 gene CpG island were determined by using the methylated DNA immunoprecipitation-quantitative PCR assay. Results: The methylation level of the ESR1 promoter observed in women with a body mass index (BMI) ≥30 kg/m2 (p ≤ 0.001) was higher than in the subgroups of women of BMI <25 kg/m2 (p < 0.001) and BMI 25-29 kg/m2 (p < 0.001) and was also higher in postmenopausal women compared with that in premenopausal women (p = 0.046). Pearson correlation coefficient analyses also showed that the high methylation of the ESR1 promoter was correlated with increasing age (r = -0.246, p = 0.007) and BMI (r = -0.331, p ≤ 0.001). Finally, linear multivariate regression revealed a significant association between high methylation rates in the ESR1 gene promoter and increased BMI (β = -0.285, 95% CI = -0.457 to -0.113, p = 0.001). Furthermore, a higher methylation level at the ESR1 gene exon 1 was found in the BMI ≥ 30 kg/m2 subgroup compared to the BMI 25-29 kg/m2 subgroup (p = 0.023). Conclusion: These findings provide new hints about the relationship between epigenetic changes within the ESR1 gene CpG island and postmenopausal obesity and aging in cancer-free women. In terms of lifestyle intervention opportunities, this study also highlights the significance and feasibility of such interventions for BMI as a modifiable risk factor. © Mary Ann Liebert, Inc. 2017.