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Updated: Apr 11, 2026

Profiling of Estrogen-regulated MicroRNAs in Breast Cancer Cells
Published on: February 21, 2014
Detection of Candidate Circular RNAs to Monitor Anti-Hormonal Response in the Mammary Gland
Nico Trummer1, Malte Weyrich1, Paige Ryan2
1Data Science in Systems Biology, School of Life Sciences, Technical University of Munich, Freising, Germany.
Abstract:
Anti-hormonal therapies such as selective estrogen receptor modulators like tamoxifen or aromatase inhibitors like letrozole represent a cornerstone for breast cancer prevention and therapy of estrogen receptor-positive breast cancer. Therapeutic monitoring can include blood tests and imaging; however, genetically-based approaches are not yet in practice. Ideally, a test would be able to detect a positive molecular response across different estrogen pathway-suppressive approaches. Circular RNAs are a species of non-coding RNAs detectable in plasma that have been proposed as non-invasive therapeutic biomarkers. To determine whether a set of specific circular RNAs is altered across estrogen-suppressive pathway approaches, we analyzed mammary gland-specific total RNA sequencing data from two individual genetically engineered mouse models (GEMMs) of estrogen pathway-induced breast cancer, with or without exposure to tamoxifen or letrozole. The nf-core/circrna pipeline was used to identify circRNAs that were differentially expressed in response to either tamoxifen or letrozole. We then screened for circRNAs that were differentially regulated by both anti-hormonals. Four up-regulated and 31 down-regulated circRNAs with host genes known to be expressed in human breast epithelial cells were identified as showing reproducible differential regulation in response to anti-hormonal treatment.
Insights
Circular RNAs show promise as non-invasive biomarkers for monitoring anti-hormonal therapy in estrogen receptor-positive breast cancer. This study identified specific circular RNAs consistently altered by tamoxifen or letrozole treatment.
Area of Science:
- Oncology
- Molecular Biology
- Biomarkers
Background:
- Anti-hormonal therapies like tamoxifen and letrozole are crucial for estrogen receptor-positive breast cancer.
- Current monitoring methods (blood tests, imaging) lack molecular specificity.
- Genetically-based, non-invasive biomarkers are needed to track treatment response.
Purpose of the Study:
- To identify specific circular RNAs (circRNAs) altered by different anti-hormonal treatments.
- To assess circRNAs as potential non-invasive biomarkers for therapeutic response.
- To find circRNAs regulated by both tamoxifen and letrozole.
Main Methods:
- Analysis of mammary gland-specific total RNA sequencing data from two genetically engineered mouse models (GEMMs).
- Utilized the nf-core/circrna pipeline to identify differentially expressed circRNAs.
- Screened for circRNAs reproducibly regulated by both tamoxifen and letrozole.
Main Results:
- Identified circRNAs differentially expressed in response to tamoxifen or letrozole.
- Found four up-regulated and 31 down-regulated circRNAs common to both treatments.
- Selected circRNAs have host genes expressed in human breast epithelial cells.
Conclusions:
- Specific circRNAs are differentially regulated by distinct anti-hormonal therapies.
- These circRNAs represent potential non-invasive biomarkers for monitoring breast cancer treatment.
- Further validation in human studies is warranted to confirm their clinical utility.

