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Updated: Feb 13, 2026

Profiling of Estrogen-regulated MicroRNAs in Breast Cancer Cells
Published on: February 21, 2014
Quantitative mapping of RNA-mediated nuclear estrogen receptor β interactome in human breast cancer cells
Giorgio Giurato1,2, Giovanni Nassa1, Annamaria Salvati1
1Laboratory of Molecular Medicine and Genomics, Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, 84081 Baronissi (SA), Italy.
Abstract:
The nuclear receptor estrogen receptor 2 (ESR2, ERβ) modulates cancer cell proliferation and tumor growth, exerting an oncosuppressive role in breast cancer (BC). Interaction proteomics by tandem affinity purification coupled to mass spectrometry was previously applied in BC cells to identify proteins acting in concert with ERβ to control key cellular functions, including gene transcription, RNA splicing and post-transcriptional mRNA regulation. These studies revealed an involvement of RNA in ERβ interactome assembly and functions. By applying native protein complex purification followed by nano LC-MS/MS before and after in vitro RNA removal, we generated a large dataset of newly identified nuclear ERβ interactors, including a subset associating with the receptor via RNA bridging. These datasets will be useful to investigate further the role of ERβ, nuclear RNAs and the other proteins identified here in BC and other cell types.
Insights
Estrogen receptor 2 (ERβ) plays a key role in breast cancer (BC) by interacting with proteins and RNA. This study identified new ERβ interactors, revealing RNA
Area of Science:
- Molecular Biology
- Cancer Research
- Proteomics
Background:
- The estrogen receptor 2 (ESR2, ERβ) is a nuclear receptor with a known oncosuppressive role in breast cancer (BC).
- Previous studies indicated that RNA is involved in the assembly and function of the ERβ interactome.
- Understanding ERβ's protein interactions is crucial for deciphering its role in BC progression.
Purpose of the Study:
- To identify novel nuclear ERβ interactors in breast cancer cells.
- To investigate the role of RNA in mediating ERβ protein complex formation.
- To provide a comprehensive dataset of ERβ-associated proteins for further research in BC.
Main Methods:
- Native protein complex purification followed by nano liquid chromatography-tandem mass spectrometry (LC-MS/MS).
- Analysis of protein-RNA interactions by comparing results before and after in vitro RNA removal.
- Interaction proteomics using tandem affinity purification coupled to mass spectrometry.
Main Results:
- A large dataset of newly identified nuclear ERβ interactors was generated.
- A subset of ERβ interactors was found to associate with the receptor via RNA bridging.
- The study confirmed the involvement of RNA in ERβ interactome assembly and function.
Conclusions:
- This research expands the understanding of ERβ's molecular interactions in breast cancer.
- The identified ERβ interactors and the role of RNA provide new avenues for BC research.
- The generated datasets can facilitate further investigations into ERβ, nuclear RNAs, and their associated proteins in BC and other cell types.
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