小RNA
乳腺癌
癌症研究
生物
癌症
报告基因
细胞凋亡
癌细胞
细胞培养
荧光素酶
基因表达
基因
分子生物学
转染
生物化学
遗传学
作者
Jin Xu,Lin Li,Qing Chen,Liantao Li
出处
期刊:PubMed
[National Institutes of Health]
日期:2023-09-20
卷期号:43 (9): 1515-1524
被引量:2
标识
DOI:10.12122/j.issn.1673-4254.2023.09.09
摘要
OBJECTIVE: To investigate the role of Hsa-miR-148a-3p in regulating biological behaviors of breast cancer cells and explore the mechanism. METHODS: TCGA database was used to identify the differential miRNAs and mRNAs in breast cancer, and the protein-protein interaction (PPI) network was constructed using String and Cytoscape to screen the top 10 hub genes and construct the miRNA-TOP10hub network. RT-qPCR was used to detect the expressions of Hsa-miR-148a-3p and DUSP1 in breast cancer tissues and cell lines. The effects of Hsa-miR-148a-3p mimic and inhibitor on proliferation, migration, invasion and apoptosis of MCF-7 cells were analyzed, and luciferase reporter gene experiment was performed to verify the binding of Hsa-miR-148a-3p to DUSP1. The effect of Hsa-miR-148a-3p overexpression on breast cancer cell xenograft growth was evaluated in nude mice. Kaplan-Meier survival curve analysis was used to analyze the survival of the tumor-bearing mice, and the expression level of DUSP1 in the xenografts was detected using immunohistochemistry. RESULTS: <0.01). CONCLUSION: Hsa-miR-148a-3p promotes malignant behavior of breast cancer cells by inhibiting the expression of DUSP1.
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