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Updated: Oct 6, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Role of miR-100-5p and CDC25A in breast carcinoma cells
Xiaoping Li1,2, Yanli Ren3, Donghong Liu4
1Faculty of Medicine, Macau University of Science and Technology, Macau, China.
Objective:
To inquiry about mechanism of miR-100-5p/CDC25A axis in breast carcinoma (BC), thus offering a new direction for BC targeted treatment.
Methods:
qRT-PCR was employed to explore miR-100-5p and CDC25A mRNA levels. Western blot was employed for detecting protein expression of CDC25A. Targeting relationship of miR-100-5p and CDC25A was verified by dual-luciferase assay. In vitro experiments were used for assessment of cell functions.
Results:
In BC tissue and cells, miR-100-5p was significantly lowly expressed (P < 0.05) while CDC25A was highly expressed. Besides, miR-100-5p downregulated CDC25A level. miR-100-5p had a marked influence on the prognosis of patients. The forced miR-100-5p expression hindered BC cell proliferation, migration and invasion, and facilitated cell apoptosis. Upregulated miR-100-5p weakened promotion of CDC25A on BC cell growth.
Conclusion:
Together, these findings unveiled that CDC25A may be a key target of miR-100-5p that mediated progression of BC cells. Hence, miR-100-5p overexpression or CDC25A suppression may contribute to BC diagnosis.
Insights
MicroRNA-100-5p (miR-100-5p) is downregulated in breast cancer (BC), while CDC25A is upregulated. Restoring miR-100-5p levels inhibits BC progression and may serve as a diagnostic marker.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Breast carcinoma (BC) is a significant global health concern.
- Understanding the molecular mechanisms driving BC progression is crucial for developing effective targeted therapies.
Purpose of the Study:
- To investigate the role of the miR-100-5p/CDC25A axis in breast carcinoma.
- To explore the potential of this axis as a therapeutic target for BC.
Main Methods:
- Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) to measure miR-100-5p and CDC25A mRNA levels.
- Western blot analysis to assess CDC25A protein expression.
- Dual-luciferase reporter assay to confirm the targeting relationship between miR-100-5p and CDC25A.
- In vitro cell function assays to evaluate the impact on BC cell proliferation, migration, invasion, and apoptosis.
Main Results:
- miR-100-5p was significantly downregulated in BC tissues and cells, whereas CDC25A was highly expressed.
- miR-100-5p directly downregulated CDC25A expression.
- Forced expression of miR-100-5p inhibited BC cell proliferation, migration, and invasion, while promoting apoptosis.
- Overexpression of miR-100-5p counteracted the promoting effects of CDC25A on BC cell growth.
- miR-100-5p expression levels correlated with patient prognosis.
Conclusions:
- CDC25A is identified as a key target of miR-100-5p in mediating BC progression.
- miR-100-5p overexpression or CDC25A suppression shows potential for BC diagnosis and targeted therapy.
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