Genetic regulation of the estrogen receptor and inherited predisposition to breast cancer

• 成果类型: Article
• 署名作者: Pierce, Sarah B.; Kortbawi, Hannah; Gulsuner, Suleyman; Mandell, Jessica B.; Lee, Ming K.; Walsh, Tom; King, Mary - Claire
• 署名单位: University of Washington; University of Washington Seattle; University of Washington; University of Washington Seattle; University of California System; University of California San Francisco; University of California System; University of California San Francisco
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2517736122
• 发表日期: 2025-10-28
• 页码: e2517736122
• 关键词: Breast cancer; estrogen receptor; inherited predisposition; noncoding regulatory variation; genome-wide association; TERT PROMOTER MUTATIONS; TFAP2C; RISK; expression; binding; variant; ESR1; methylation; mechanisms

摘要

For many families severely affected with breast cancer, no inherited causal allele has been detected in any tumor suppressor gene. In an effort to understand the genetics underlying breast cancer in these families, we evaluated 136 such families for coinheritance of breast cancer with each of 79 common variants reported as high-confidence risk alleles for breast cancer by meta-analyses of genome-wide association studies. Simulations based on allele frequencies and family structures revealed one (and only one) of these 79 variants to cosegregate with breast cancer in the families significantly more frequently than expected by chance. This variant (rs2046210) is located 180 kb proximal to ESR1, encoding the estrogen receptor alpha. Reporter assays in MCF7 cells revealed enhancement by the genomic segment at this site of activity of ESR1 promoters, but no difference in effect among alternative haplotypes. In contrast, the 600 kb genomic region including ESR1 and rs2046210 harbored 11 rare variants, each of which cosegregated with breast cancer in one or a few families. For 9 of these 11 variants, reporter assays indicated significant allele-specific effects on ESR1 promoters, with the breast-cancer-linked allele of each variant yielding higher promoter activity. At the site with the most striking effect, the breast-cancer-linked allele was associated with increased binding by transcription factor AP2-gamma TFAP2C in both MCF7 and T47D cells. These results demonstrate coinheritance with breast cancer of rare alleles that increase activity of ESR1 promoters, and suggest that rare ESR1 regulatory alleles may contribute to inherited predisposition to breast cancer.