Conclusion
Our findings confirmed that miRNA-145-5p hindered malignant progression of breast cancer by negatively regulating H2AFX. MiRNA-145-5p/H2AFX axis may be a novel therapeutic target for breast cancer.
Methods
qRT-PCR detected miRNA-145-5p and histone protein family member X (H2AFX) mRNA expression in breast cancer cells, and western blot determined the protein expression of H2AFX. After predicting the target genes via the bioinformatics methods, the targeting relationship between miRNA-145-5p and H2AFX was verified by dual-luciferase, RIP, and RNA pull-down assays. The relationship between H2AFX and clinical indexes was also analyzed. Furthermore, the effects of miRNA-145-5p/H2AFX regulatory axis on breast cancer cell progression were determined by colony formation, wound healing, CCK-8, and Transwell assays.
Objective
Our study is aimed at exploring how miRNA-145-5p functions in breast cancer cells.
Results
The results suggested that miRNA-145-5p was markedly lowly-expressed in breast cancer tissue and cells, while H2AFX was upregulated, which had a positive correlation with T stages of breast cancer. Besides, overexpressed miRNA-145-5p was found to remarkably suppress progression of breast cancer cells. As bioinformatic analysis predicted that H2AFX was the potential target of miRNA-145-5p, the dual-luciferase assay was conducted, which demonstrated that miRNA-145-5p negatively regulated the expression of H2AFX by targeting its 3'-UTR. The rescue experiment demonstrated that overexpression of miRNA-145-5p could offset the promotion effects of oe-H2AFX on malignant progression. Objective: Our study is aimed at exploring how miRNA-145-5p functions in breast cancer cells.