基因敲除
癌变
小RNA
癌症研究
肺癌
下调和上调
细胞生长
生物
细胞周期
细胞
癌症
细胞培养
医学
肿瘤科
基因
遗传学
作者
Yingnan Yang,Lu‐Qin Bian,Xiaodong Ling,Chengyuan Fang,Shulin Jiang
标识
DOI:10.1016/j.prp.2019.152555
摘要
Recent evidence highlights that microRNAs serve as crucial regulators of tumorigenesis, including non-small cell lung cancer (NSCLC). The present study was designed to investigate the expression profile, clinical significance and biological role of miR-421 in NSCLC. The results showed that miR-421 expression was markedly increased in NSCLC tissues and cell lines. Further experimental data indicated that knockdown of miR-421 significantly inhibited NSCLC cell proliferation and induced cell cycle arrest in vitro. The migratory and invasive abilities of NSCLC cells were also attenuated following miR-421 knockdown. Furthermore, PDCD4 was identified as a direct target of miR-421, and its expression was inversely correlated with miR-421 expression in NSCLC tissues. PDCD4 also abrogated the oncogenic role of miR-421 in NSCLC cells. Collectively, our study revealed that miR-421 is significantly upregulated in NSCLC and might represent a potential therapeutic target for NSCLC patients.
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