细胞生长
癌症研究
基因沉默
下调和上调
小RNA
上皮-间质转换
肝细胞癌
医学
癌症
细胞凋亡
基因敲除
细胞迁移
细胞
细胞周期
细胞培养
细胞生物学
肝癌
转染
转移
生物
内科学
基因
遗传学
作者
Zheyue Shu,Feng Gao,Qi Xia,Min Zhang
标识
DOI:10.2217/bmm-2020-0322
摘要
Objective: This study aimed to observe the effect of miR-9-5p and CPEB3 on hepatocellular carcinoma (HCC) cells, and investigate the underlying targeting regulatory mechanism. Materials & methods: Various experiments like CCK-8, colony formation assay, wound healing assay and Transwell were performed for cancer cell activities detection, including cell proliferation, growth activity, migration and invasion. Results: MiR-9-5p was found to be highly expressed in HCC cells, while CPEB3 was poorly expressed (p < 0.05). The overexpression of miR-9-5p and the silencing of CPEB3 both could significantly promote cell proliferation, migration and invasion (p < 0.05). In addition, miR-9-5p could target to downregulate CPEB3 expression, thus accelerating cell proliferation, migration, invasion and epithelial-mesenchymal transition process in HCC. Conclusion: MiR-9-5p can target CPEB3, thereby promoting cell proliferation, migration and invasion in HCC. The axis of miR-9-5p/CPEB3 is expected to become a potential therapeutic target beneficial for HCC patients.
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