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Updated: Mar 29, 2026

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Clinicopathological Analysis of miRNA Expression in Breast Cancer Tissues by Using miRNA In Situ Hybridization
Published on: June 7, 2016
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Circulating MicroRNA in Breast Cancer
Alexander Sturzu1, Ruixia Ma1, Yaguang Xi1,2
1Department of Pharmaceutical and Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602, USA.
Cancers
|March 28, 2026
Summary
Extracellular microRNAs (miRNAs) show promise as breast cancer biomarkers and therapeutic targets, but their clinical use requires standardized, subtype-aware approaches for accurate diagnosis and personalized treatment.
Area of Science:
- Molecular Biology and Genetics
- Oncology
- Biomarker Discovery
Background:
- Triple-negative breast cancer (TNBC) remains a clinical challenge despite advances in diagnostics and personalized medicine.
- Extracellular microRNAs (miRNAs) are gene regulators found in biofluids, protected by vesicles or proteins.
- This review focuses on extracellular miRNAs in breast cancer, their subtype-specific roles, and potential as liquid-biopsy biomarkers.
Purpose of the Study:
- To review current evidence on oncogenic and tumor-suppressive extracellular miRNAs in breast cancer.
- To emphasize subtype-specific functions and clinical relevance of miRNAs as biomarkers and therapeutic targets.
- To synthesize findings on circulating miRNAs for diagnosis, prognosis, and treatment response prediction.
Main Methods:
- PubMed literature review (January 2000-February 2026) using combined search terms for breast cancer and circulating miRNAs.
- Prioritization of studies with validated targets, mechanisms, or clinical evidence for diagnostic/prognostic utility.
- Subtype-aware evaluation of findings, organized by functional categories and clinical/translational studies.
Main Results:
- miR-21 and miR-155 identified as prominent oncogenic miRNAs; miR-205 as a tumor-suppressive miRNA.
- Circulating miRNA panels show potential for sensitive and specific breast cancer diagnostics.
- Subtype-dependent miRNA effects observed, with opposing roles in TNBC versus ER-positive breast cancer.
Conclusions:
- Circulating miRNAs are promising minimally invasive biomarkers and potential therapeutic targets for breast cancer.
- Clinical translation is limited by biological context dependence and pre-analytical/analytical variability.
- Standardized, subtype-aware protocols and validated panels are crucial for clinical implementation and precision oncology.
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