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Updated: Oct 12, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
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.
Abstract:
MicroRNAs (miRNAs/miRs) function as key regulators in breast cancer (BC). The present study aimed to verify the function and molecular regulation of miR-337-3p in BC cells. Bioinformatics analysis was performed to screen key genes and miRNAs associated with BC. Reverse transcription-quantitative PCR and western blot analyses were performed to detect RNA and protein expression levels. Cell Counting Kit-8, BrdU and cell adhesion assays, and flow cytometric analysis were performed to assess the biological behaviors of BC cells. The dual-luciferase reporter, RNA pull-down assays, and Pearson's correlation analysis were performed to determine the association between miRNAs and mRNAs. Bioinformatics analysis revealed that miR-337-3p and cyclin-dependent kinase 1 (CDK1) acted as key regulators in BC. In addition, miR-337-3p was expressed at low levels in BC cells and tissues, which suppressed BC progression. CDK1 expression was upregulated in BC cells and tissues, which was associated with increased cell proliferation and adhesion, as well as decreased apoptosis in BC. Notably, miR-337-3p targeted CDK1 to inhibit BC cell progression. Taken together, the results of the present study suggest that miR-337-3p plays a tumor-suppressive role in BC by targeting CDK1.
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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