作者: Jun Yin , Chengyin Weng , Jieke Ma , Fanfan Chen , Yecai Huang
关键词: Ectopic expression 、 Gene knockdown 、 Cell 、 Cell growth 、 microRNA 、 Deubiquitinating Enzyme CYLD 、 Cancer research 、 Molecular biology 、 Cell cycle 、 Biology 、 Ubiquitin Carboxyl-Terminal Hydrolase CYLD
摘要: Previous studies have demonstrated that microRNAs (miRs) are important regulators involved in various cancers, including human glioblastoma (GBM). However, the underlying mechanism of miR‑1288 remains poorly understood, and its role GBM has not been reported. The present study confirmed expression was markedly upregulated GBM. Ectopic promoted prolife-ration, colony formation anchorage‑independent growth cells. Bioinformatics analysis coupled with western blotting luciferase report assays also indicated cell proliferation by targeting ubiquitin carboxyl‑terminal hydrolase (CYLD). Knockdown CYLD reversed promotion miR‑1288‑in These results suggest miR‑1288/CYLD axis may represent a potential therapeutic target for treatment