| Literature DB >> 26883008 |
Jiangqiao Geng1, Yuanhu Liu1, Yaqiong Jin1, Jun Tai2, Jie Zhang2, Xiao Xiao2, Ping Chu1, Yongbo Yu1, Sheng Cai Wang2, Jie Lu1, Shujing Han1, Jin Shi1, Yongli Guo1, Xin Ni1.
Abstract
MicroRNAs (miRNAs) are increasingly recognized as oncogenes or tumor suppressors in laryngeal squamous cell carcinoma (LSCC). In this study, we analyzed the roles of miR-365a-3p, miR-143-5p, and miR-494-3p in LSCC using Annexin V/propidium iodide double staining and flow cyto-metry, along with a Transwell migration and invasion assay. The results showed that miR-365a-3p inhibitor significantly facilitated cell apoptosis and suppressed cell cycle progression, migration, and invasion in Hep-2 cells. However, miR-143-5p and miR-494-3p had no such influences. We then investigated the role of miR-365a-3p in LSCC in vivo and found that miR-365a-3p inhibitor suppressed LSCC xenograft tumor growth and metastasis in xenograft mouse models. Moreover, miR-365a-3p inhibitor significantly decreased the expression of p-AKT (Ser473), which indicated that miR-365a-3p can mediate PI3K/AKT signaling pathway transduction via p-AKT (Ser473) in LSCC. The data suggest that miR-365a-3p may act as an oncomiR and may promote growth and metastasis in LSCC via the PI3K/AKT signaling pathway, and thus miR‑365a-3p may be a potential therapeutic target for treatment of LSCC.Entities:
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Year: 2016 PMID: 26883008 DOI: 10.3892/or.2016.4617
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906