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.

Abstract

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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