Du Yu, Li Yang, Lv Hanxiao, Zhou Songcheng, Sun Zhen, Wang Min
Department of Endodontics, School and Hospital of Stomatology, Wenzhou Medical University Wenzhou, 325000, PR China.
Department of Gastroenterology, Jining NO.1 People's Hospital Jining, Shandong, 272011, PR China.
Int J Clin Exp Pathol. 2015 Oct 1;8(10):12252-9. eCollection 2015.
Increasing evidences indicate that dysregulation of miRNAs contributes to the pathogenesis of oral squamous cell carcinoma (OSCC). However, little is known about the potential role of miR-98 in OSCC. Here, we found that miR-98 was downregulated in OSCC tissues and cell lines. Overexpression of miR-98 inhibited proliferation, colony formation, migration, and invasion of OSCC cells. IGF1R was identified as the potential target of miR-98 using dual luciferase assay, qRT-PCR and western blot. Furthermore, restoration of IGF1R remarkably reversed the tumor-suppressive effects of miR-98 on OSCC cells. Moreover, miR-98 expression was inversely correlated with IGF1R expression in 19 cases of OSCC. These findings suggest that miR-98 inhibits cancer cell growth and metastasis by direct targeting IGF1R, implicating miR-98 as a novel potential therapeutic target for OSCC.
越来越多的证据表明,微小RNA(miRNA)失调与口腔鳞状细胞癌(OSCC)的发病机制有关。然而,关于miR-98在OSCC中的潜在作用知之甚少。在此,我们发现miR-98在OSCC组织和细胞系中表达下调。miR-98的过表达抑制了OSCC细胞的增殖、集落形成、迁移和侵袭。通过双荧光素酶报告基因检测、qRT-PCR和蛋白质印迹法确定胰岛素样生长因子1受体(IGF1R)为miR-98的潜在靶标。此外,恢复IGF1R的表达显著逆转了miR-98对OSCC细胞的肿瘤抑制作用。此外,在19例OSCC中,miR-98表达与IGF1R表达呈负相关。这些发现表明,miR-98通过直接靶向IGF1R抑制癌细胞生长和转移,提示miR-98作为OSCC一种新的潜在治疗靶点。