MicroRNA-337-3p impedes breast cancer progression by targeting cyclin-dependent kinase 1

Shuxin Kong1, Jianyang Liu2, Bin Zhang1

  • 1Department of Breast Surgery, The People's Hospital of Zhengzhou University, Henan Provincial People's Hospital, Zhengzhou, Henan 450003, P.R. China.

Oncology Letters
|November 25, 2021
PubMed

Insights

MicroRNAs (miRNAs) regulate breast cancer (BC). Low levels of miR-337-3p suppress BC progression by targeting cyclin-dependent kinase 1 (CDK1), indicating a tumor-suppressive role.

Area of Science:

  • Molecular Biology
  • Oncology
  • Genetics

Background:

  • MicroRNAs (miRNAs) are crucial regulators in various cancers, including breast cancer (BC).
  • Dysregulation of specific miRNAs can significantly impact BC development and progression.
  • Understanding miRNA functions is vital for identifying novel therapeutic targets in BC.

Purpose of the Study:

  • To investigate the role and molecular mechanism of miR-337-3p in breast cancer cells.
  • To identify key regulatory genes and miRNAs associated with BC progression.
  • To elucidate the relationship between miR-337-3p and its potential target gene, CDK1.

Main Methods:

  • Bioinformatics analysis to identify key regulatory molecules in BC.
  • Quantitative PCR and Western blot to assess RNA and protein expression levels.
  • Cell proliferation, adhesion, and apoptosis assays to evaluate BC cell behavior.
  • Dual-luciferase reporter and RNA pull-down assays to confirm miRNA-mRNA interactions.

Main Results:

  • miR-337-3p was found to be downregulated in BC cells and tissues, suppressing tumor progression.
  • Cyclin-dependent kinase 1 (CDK1) was upregulated in BC, correlating with increased proliferation and adhesion, and decreased apoptosis.
  • miR-337-3p directly targets CDK1, thereby inhibiting BC cell progression.

Conclusions:

  • miR-337-3p exhibits a tumor-suppressive function in breast cancer.
  • The miR-337-3p/CDK1 axis represents a potential therapeutic target for BC treatment.

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