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Updated: Feb 8, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
MicroRNAs in regulation of triple-negative breast cancer progression
Dominika Piasecka1, Marcin Braun1,2, Radzislaw Kordek1
1Department of Pathology, Medical University of Lodz, Lodz, Poland.
Purpose:
Dysregulation of miRNA profile has been associated with a broad spectrum of cellular processes underlying progression of various human malignancies. Increasing evidence suggests that specific microRNA clusters might be of clinical utility, especially in triple-negative breast carcinoma (TNBC), devoid of both predictive markers and potential therapeutic targets. Here we provide a comprehensive review of the existing data on microRNAs in TNBC, their molecular targets, a putative role in invasive progression with a particular emphasis on the epithelial-to-mesenchymal transition (EMT) and acquisition of stem-cell properties (CSC), regarded both as prerequisites for metastasis, and significance for therapy.
Methods:
PubMed and Medline databases were systematically searched for the relevant literature. 121 articles have been selected and thoroughly analysed.
Results:
Several miRNAs associated with EMT/CSC and invasion were identified as significantly (1) upregulated: miR-10b, miR-21, miR-29, miR-9, miR-221/222, miR-373 or (2) downregulated: miR-145, miR-199a-5p, miR-200 family, miR-203, miR-205 in TNBC. Dysregulation of miR-10b, miR-21, miR-29, miR-145, miR-200 family, miR-203, miR-221/222 was reported of prognostic value in TNBC patients.
Conclusion:
Available data suggest that specific microRNA clusters might play an important role in biology of TNBC, understanding of which should assist disease prognostication and therapy.
Insights
Specific microRNAs are dysregulated in triple-negative breast carcinoma (TNBC), impacting invasion and stemness. Understanding these microRNA profiles aids in TNBC prognostication and therapy development.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA (miRNA) dysregulation is implicated in various human cancers.
- Triple-negative breast carcinoma (TNBC) lacks predictive markers and therapeutic targets.
- Specific miRNA clusters may hold clinical utility in TNBC management.
Purpose of the Study:
- To comprehensively review microRNAs in TNBC.
- To analyze miRNA targets and their roles in invasion, epithelial-to-mesenchymal transition (EMT), and cancer stem cell (CSC) properties.
- To assess the significance of miRNAs for TNBC therapy.
Main Methods:
- Systematic literature search of PubMed and Medline databases.
- Analysis of 121 selected articles on microRNAs in TNBC.
- Identification of significantly up- or down-regulated miRNAs associated with EMT/CSC and invasion.
Main Results:
- Upregulated miRNAs in TNBC include miR-10b, miR-21, miR-29, miR-9, miR-221/222, and miR-373.
- Downregulated miRNAs in TNBC include miR-145, miR-199a-5p, miR-200 family, miR-203, and miR-205.
- Dysregulation of specific miRNAs (e.g., miR-10b, miR-21, miR-200 family) shows prognostic value in TNBC patients.
Conclusions:
- Specific microRNA clusters play a crucial role in TNBC biology.
- Understanding these miRNA roles can improve TNBC prognostication.
- MicroRNAs offer potential for developing novel TNBC therapies.
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