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LRH-1 Governs Vital Transcriptional Programs in Endocrine-Sensitive and -Resistant Breast Cancer Cells
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Zeitschriftentitel: | Cancer Research |
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Personen und Körperschaften: | , , , , |
In: | Cancer Research, 74, 2014, 7, S. 2015-2025 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
American Association for Cancer Research (AACR)
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Schlagwörter: |
Zusammenfassung: | <jats:title>Abstract</jats:title> <jats:p>Tumor characteristics are decisive in the determination of treatment strategy for patients with breast cancer. Patients with estrogen receptor α (ERα)–positive breast cancer can benefit from long-term hormonal treatment. Nonetheless, the majority of patients will develop resistance to these therapies. Here, we investigated the role of the nuclear receptor liver receptor homolog-1 (LRH-1, NR5A2) in antiestrogen-sensitive and -resistant breast cancer cells. We identified genome-wide LRH-1–binding sites using ChIP-seq (chromatin immunoprecipitation sequencing), uncovering preferential binding to regions distal to transcriptional start sites. We further characterized these LRH-1–binding sites by integrating overlapping layers of specific chromatin marks, revealing that many LRH-1–binding sites are active and could be involved in long-range enhancer–promoter looping. Combined with transcriptome analysis of LRH-1–depleted cells, these results show that LRH-1 regulates specific subsets of genes involved in cell proliferation in antiestrogen-sensitive and antiestrogen-resistant breast cancer cells. Furthermore, the LRH-1 transcriptional program is highly associated with a signature of poor outcome and high-grade breast cancer tumors in vivo. Herein, we report the genome-wide location and molecular function of LRH-1 in breast cancer cells and reveal its therapeutic potential for the treatment of breast cancers, notably for tumors resistant to treatments currently used in therapies. Cancer Res; 74(7); 2015–25. ©2014 AACR.</jats:p> |
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Umfang: | 2015-2025 |
ISSN: |
0008-5472
1538-7445 |
DOI: | 10.1158/0008-5472.can-13-2351 |