Therapeutic potential of MicroRNAs in targeting breast cancer stem cells: A systematic review

Joyce Zhin Shi Ting1, Joelyn Lim1, Tiffany Yan Yue Cho1

  • 1School of Pharmacy, Monash University, Malaysia.

Abstract

Insights

MicroRNAs (miRNAs) show promise in targeting breast cancer stem cells (BCSCs) by suppressing their growth and spread. Further research is needed to develop safe and effective miRNA-based therapies for breast cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Breast cancer stem cells (BCSCs) drive poor therapeutic outcomes due to high proliferation, metastasis, and treatment resistance.
  • MicroRNAs (miRNAs) are key regulators of tumor biology, but their role in BCSCs is not fully understood.
  • Understanding miRNA regulation of BCSCs is crucial for developing novel breast cancer treatments.

Purpose of the Study:

  • To systematically review in vitro and in vivo studies on miRNA regulation of BCSCs.
  • To evaluate the potential of miRNA-based strategies for targeting BCSCs.
  • To identify miRNAs that can suppress BCSC proliferation, metastasis, and treatment resistance.

Main Methods:

  • Systematic literature search of major scientific databases (2015-2024).
  • Screening of studies investigating miRNA effects on BCSCs based on inclusion criteria.

Main Results:

  • Sixteen miRNAs were identified with regulatory effects on BCSCs across 20 studies.
  • Most miRNAs exhibited tumor-suppressive functions, inhibiting proliferation, stemness, metastasis, and resistance.
  • miR-7 was consistently identified as a potent tumor-suppressive miRNA with broad inhibitory effects.

Conclusions:

  • miRNAs are promising therapeutic targets for BCSCs, coordinating the regulation of proliferation, resistance, and metastasis.
  • Advancing miRNA-based strategies requires standardized experimental designs and further mechanistic studies.
  • Ensuring the safety and efficacy of miRNA therapies across breast cancer subtypes necessitates expanded in vivo research.

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